Een studie van chemotherapie en Ramucirumab versus alleen chemotherapie bij deelnemers aan tweedelijns niet-kleincellige longkanker (NSCLC) die eerder eerstelijns chemotherapie op basis van platina kregen
10 september 2019 bijgewerkt door: Eli Lilly and Company
Een gerandomiseerde, dubbelblinde, fase 3-studie van docetaxel en ramucirumab versus docetaxel en placebo bij de behandeling van niet-kleincellige longkanker in stadium IV na progressie van de ziekte na één eerdere op platina gebaseerde therapie
Het doel van de studie is om de overleving van deelnemers die chemotherapie en ramucirumab krijgen te vergelijken met alleen chemotherapie als tweedelijnsbehandeling voor NSCLC na eerdere eerstelijns chemotherapie op basis van platina.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
1253
Fase
- Fase 3
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Buenos Aires, Argentinië, C1417EYG
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Córdoba, Argentinië, X5016KEH
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La Rioja, Argentinië, 5300
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Rosario, Argentinië, 2000
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Tucumain, Argentinië, 4000
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Viedma, Argentinië, 8500
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Barretos, Brazilië, 14784700
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Belo Horizonte, Brazilië, 31110580
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Goiania, Brazilië, 74140050
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Porto Alegre, Brazilië, 90430-090
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São Paulo, Brazilië, 1224010
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Alberta
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Edmonton, Alberta, Canada, T6G 1Z2
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New Brunswick
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Moncton, New Brunswick, Canada, E1C 6Z8
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Quebec
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Sainte-Foy, Quebec, Canada, G1V 4G5
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Augsburg, Duitsland, 86150
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Bad Soden, Duitsland, 65812
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Bielefeld, Duitsland, 33611
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Dresden, Duitsland, 01307
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Frankfurt, Duitsland, 60596
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Gerlingen, Duitsland, 70839
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Großhansdorf, Duitsland, 22927
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Halle, Duitsland, 06120
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Heidelberg, Duitsland, 69126
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Immenhausen, Duitsland, 34376
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Oldenburg, Duitsland, 26121
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Ulm, Duitsland, 89081
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Villingen-Schwenningen, Duitsland, 78050
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Grenoble, Frankrijk, 38049
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Lille, Frankrijk, 59037
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Lyon, Frankrijk, 69373
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Nice, Frankrijk, 06050
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Strasbourg, Frankrijk, 67091
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Toulouse, Frankrijk, 31059
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Vandoeuvre Les Nancy, Frankrijk, 54511
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Athens, Griekenland, 10676
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Chania, Griekenland, 73300
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Kifissia, Griekenland, 14564
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Patras, Griekenland, 26500
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Budapest, Hongarije, 1145
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Gyula, Hongarije, 5703
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Matrahaza, Hongarije, 3233
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Nyiregyhaza, Hongarije, 4412
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Pécs, Hongarije, 7623
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Szekesfehervar, Hongarije, 8000
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Bangalore, Indië, 560099
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Cuttack, Indië, 753007
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Delhi, Indië, 110085
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Jaipur, Indië, 302017
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Kochin, Indië, 628040
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Madurai, Indië, 625020
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Mumbai, Indië, 400 012
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Pune, Indië, 411001
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Trivandrum, Indië, 695 011
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Haifa, Israël, 31096
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Jerusalem, Israël, 91120
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Kfar Saba, Israël, 44281
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Petah Tikva, Israël, 49100
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Safed, Israël, 13110
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Tel-Aviv, Israël, 64239
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Livorno, Italië, 57124
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Monza, Italië, 20900
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Novara, Italië, 28100
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Padova, Italië, 35128
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Palermo, Italië, 90146
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Parma, Italië, 43100
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Pisa, Italië, 56124
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Rome, Italië, 00152
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Ankara, Kalkoen, 06500
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Istanbul, Kalkoen, 81540
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Izmir, Kalkoen, 35340
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Kayseri, Kalkoen, 38039
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Incheon, Korea, republiek van, 405-760
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Seoul, Korea, republiek van, 120-752
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Suwon-City, Korea, republiek van, 442-723
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Guadalajara, Mexico, 44280
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Mexico City, Mexico, 14000
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Amsterdam, Nederland, 1091AC
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Arnhem, Nederland, 6815 AD
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Harderwijk, Nederland, 3844 DG
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S-Hertogenbosch, Nederland, 5223 GZ
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Zwolle, Nederland, 80211 JW
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Grafton, Nieuw-Zeeland, 1023
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Wellington, Nieuw-Zeeland, 6002
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Oslo, Noorwegen, 0310
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Tromsø, Noorwegen, 9012
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Graz, Oostenrijk, 8036
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Grimmenstein, Oostenrijk, 2840
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Vienna, Oostenrijk, A-1140
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Wels, Oostenrijk, 4600
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Gdansk, Polen, 80-219
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Gdynia, Polen, 81-519
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Glucholazy, Polen, 48-340
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Krakow, Polen, 31-202
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lodz, Polen, 90-242
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Opole, Polen, 45-060
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Otwock, Polen, 05-400
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Poznan, Polen, 60-693
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Bayamon, Puerto Rico, 00959
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Bucharest, Roemenië, 022328
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Cluj-Napoca, Roemenië, 400058
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Iasi, Roemenië, 700106
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Moscow, Russische Federatie, 115478
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Saint Petersburg, Russische Federatie, 197758
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Stavropol, Russische Federatie, 355047
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Barcelona, Spanje, 08003
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Girona, Spanje, 17007
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Las Palmas De Gran Canaria, Spanje, 35016
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Madrid, Spanje, 28050
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Mataró, Spanje, 08304
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Pamplona, Spanje, 31008
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Pozuelo De Alarcon, Spanje, 28223
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kaohsiung, Taiwan, 813
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kuei Shan Hsiang, Taiwan, 33305
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Neihu Taipei, Taiwan, 114
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Niao Sung Hsiang, Taiwan, 833
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Taichung, Taiwan, 40705
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Taipei, Taiwan, 11031
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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East Yorkshire
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Cottingham, East Yorkshire, Verenigd Koninkrijk, HU16 5JQ
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Greater London
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London, Greater London, Verenigd Koninkrijk, W6 8RF
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lancashire
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Preston, Lancashire, Verenigd Koninkrijk, PR2 9HT
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Manchester
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Wythenshawe, Manchester, Verenigd Koninkrijk, M23 9LT
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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North Lincolnshire
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Scunthorpe, North Lincolnshire, Verenigd Koninkrijk, DN15 7BH
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Scotland
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Glasgow, Scotland, Verenigd Koninkrijk, G12 0YN
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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West Midlands
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Coventry, West Midlands, Verenigd Koninkrijk, CV2 2DX
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wolverhampton, West Midlands, Verenigd Koninkrijk, WV10 0QP
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Arizona
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Phoenix, Arizona, Verenigde Staten, 85016
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Sedona, Arizona, Verenigde Staten, 86336
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Arkansas
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Fayetteville, Arkansas, Verenigde Staten, 72703
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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California
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Alhambra, California, Verenigde Staten, 91801
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Duarte, California, Verenigde Staten, 91010
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Fresno, California, Verenigde Staten, 93720
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Fullerton, California, Verenigde Staten, 92835
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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La Jolla, California, Verenigde Staten, 92093
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Long Beach, California, Verenigde Staten, 90813
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Los Angeles, California, Verenigde Staten, 90095
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Northridge, California, Verenigde Staten, 91325
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Redondo Beach, California, Verenigde Staten, 90277
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Santa Barbara, California, Verenigde Staten, 93105
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Santa Monica, California, Verenigde Staten, 93454
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Colorado
-
Denver, Colorado, Verenigde Staten, 80218
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Connecticut
-
Waterbury, Connecticut, Verenigde Staten, 06708
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Florida
-
Jacksonville, Florida, Verenigde Staten, 32204
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Miami, Florida, Verenigde Staten, 33176
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Ocala, Florida, Verenigde Staten, 34471
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Orlando, Florida, Verenigde Staten, 32806
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Georgia
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Athens, Georgia, Verenigde Staten, 30607
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Augusta, Georgia, Verenigde Staten, 30901
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Lawrenceville, Georgia, Verenigde Staten, 30045
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Macon, Georgia, Verenigde Staten, 31201
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Rome, Georgia, Verenigde Staten, 30165
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Savannah, Georgia, Verenigde Staten, 31405
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
-
Illinois
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Springfield, Illinois, Verenigde Staten, 62703
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Indiana
-
Bloomington, Indiana, Verenigde Staten, 47402
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Iowa
-
Cedar Rapids, Iowa, Verenigde Staten, 52402
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Iowa City, Iowa, Verenigde Staten, 52242
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Kansas
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Overland Park, Kansas, Verenigde Staten, 66210
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Wichita, Kansas, Verenigde Staten, 67214
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Kentucky
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Ashland, Kentucky, Verenigde Staten, 41101
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Mount Sterling, Kentucky, Verenigde Staten, 40353
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Louisiana
-
Baton Rouge, Louisiana, Verenigde Staten, 70809
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Metairie, Louisiana, Verenigde Staten, 70006
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Maryland
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Bethesda, Maryland, Verenigde Staten, 20817
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Chevy Chase, Maryland, Verenigde Staten, 20815
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Massachusetts
-
Boston, Massachusetts, Verenigde Staten, 02115
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Danvers, Massachusetts, Verenigde Staten, 01923
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Framingham, Massachusetts, Verenigde Staten, 01701
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Newton, Massachusetts, Verenigde Staten, 02462
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Michigan
-
Ann Arbor, Michigan, Verenigde Staten, 48109
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
-
Minnesota
-
Minneapolis, Minnesota, Verenigde Staten, 55404
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
-
Missouri
-
Columbia, Missouri, Verenigde Staten, 65201
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Joplin, Missouri, Verenigde Staten, 64804
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Saint Louis, Missouri, Verenigde Staten, 63110
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
-
Montana
-
Billings, Montana, Verenigde Staten, 59101
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
-
Nevada
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Henderson, Nevada, Verenigde Staten, 89169
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Reno, Nevada, Verenigde Staten, 89502
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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New Hampshire
-
Lebanon, New Hampshire, Verenigde Staten, 03756
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Portsmouth, New Hampshire, Verenigde Staten, 03801
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New Mexico
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Albuquerque, New Mexico, Verenigde Staten, 87109
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New York
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Bronx, New York, Verenigde Staten, 10467
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Latham, New York, Verenigde Staten, 12110
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New York, New York, Verenigde Staten, 10021
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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North Carolina
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Durham, North Carolina, Verenigde Staten, 27704
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Raleigh, North Carolina, Verenigde Staten, 27607
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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North Dakota
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Fargo, North Dakota, Verenigde Staten, 58122
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Ohio
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Columbus, Ohio, Verenigde Staten, 43219
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Oklahoma
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Tulsa, Oklahoma, Verenigde Staten, 74136
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Pennsylvania
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Abington, Pennsylvania, Verenigde Staten, 19001
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kingston, Pennsylvania, Verenigde Staten, 18704
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Philadelphia, Pennsylvania, Verenigde Staten, 19106
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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South Carolina
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Charleston, South Carolina, Verenigde Staten, 29414
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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South Dakota
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Sioux Falls, South Dakota, Verenigde Staten, 57104
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Tennessee
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Chattanooga, Tennessee, Verenigde Staten, 37403
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Memphis, Tennessee, Verenigde Staten, 38138
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Texas
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Abilene, Texas, Verenigde Staten, 79606
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Amarillo, Texas, Verenigde Staten, 79106
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Beaumont, Texas, Verenigde Staten, 77702
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Bedford, Texas, Verenigde Staten, 76022
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Dallas, Texas, Verenigde Staten, 75231
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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El Paso, Texas, Verenigde Staten, 79915
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Fort Worth, Texas, Verenigde Staten, 76104
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lewisville, Texas, Verenigde Staten, 75067
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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McAllen, Texas, Verenigde Staten, 78503
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Mesquite, Texas, Verenigde Staten, 75150
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Midland, Texas, Verenigde Staten, 79701
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Odessa, Texas, Verenigde Staten, 79761
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Paris, Texas, Verenigde Staten, 75460
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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San Antonio, Texas, Verenigde Staten, 78229
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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San Antonio, Texas, Verenigde Staten, 78212
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Sherman, Texas, Verenigde Staten, 75090
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Sugar Land, Texas, Verenigde Staten, 77479
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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The Woodlands, Texas, Verenigde Staten, 77380
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Tyler, Texas, Verenigde Staten, 75702
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Webster, Texas, Verenigde Staten, 77598
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wichita Falls, Texas, Verenigde Staten, 76310
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Virginia
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Christiansburg, Virginia, Verenigde Staten, 24073
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Fairfax, Virginia, Verenigde Staten, 22031
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Newport News, Virginia, Verenigde Staten, 23601
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Richmond, Virginia, Verenigde Staten, 23298
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Washington
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Lacey, Washington, Verenigde Staten, 98503
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Spokane, Washington, Verenigde Staten, 99216
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wenatchee, Washington, Verenigde Staten, 98801
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wisconsin
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Madison, Wisconsin, Verenigde Staten, 53705
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Eskilstuna, Zweden, 63188
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Linkoping, Zweden, 58185
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lund, Zweden, 22185
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Solna, Zweden, 17176
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Basel, Zwitserland, CH-4031
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Bern, Zwitserland, CH-3010
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Fribourg, Zwitserland, 1708
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Luzern, Zwitserland, CH-6000
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Zurich, Zwitserland, CH-8091
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusiecriteria:
- Ziekteprogressie tijdens of na een eerdere eerstelijns chemotherapie op basis van platina met of zonder onderhoudstherapie
- Voorafgaande bevacizumab als eerstelijns- en/of onderhoudstherapie is toegestaan
- Ondertekende geïnformeerde toestemming
- Eastern Cooperative Oncology Group (ECOG) prestatiestatus van 0-1
- Histologisch of cytologisch bevestigd NSCLC
- Stadium IV NSCLC-ziekte
- Deelnemers hebben een meetbare of niet-meetbare ziekte
Adequate orgaanfunctie, gedefinieerd als:
- Totaal bilirubine minder dan of gelijk aan de bovengrens van normaal (ULN),
- Aspartaat Aminotransferase (AST) en Alanine Aminotransaminase (ALT) minder dan of gelijk aan 2,5 x ULN, of minder dan of gelijk aan 5 x ULN als de verhoging van de transferase te wijten is aan levermetastasen,
- Serumcreatinine lager dan of gelijk aan 1,5 x ULN of berekende creatinineklaring groter dan of gelijk aan 50 milliliter per minuut (ml/min) (volgens de Cockcroft-Gault-formule of equivalent en/of 24-uurs urineverzameling),
- Absoluut aantal neutrofielen (ANC) groter dan of gelijk aan 1,5 x 10^3/microliter (µL), hemoglobine groter dan of gelijk aan 10,0 gram/deciliter (g/dL) en bloedplaatjes groter dan of gelijk aan 100 x 10^3 /µL,
- Adequate stollingsfunctie zoals gedefinieerd door International Normalized Ratio (INR) kleiner dan of gelijk aan 1,5, of protrombinetijd en partiële tromboplastinetijd kleiner dan of gelijk aan 1,5 x ULN.
- De deelnemer heeft geen cirrose op een niveau van Child-Pugh B (of erger) of cirrose (in welke mate dan ook) en een voorgeschiedenis van hepatische encefalopathie of klinisch relevante ascites als gevolg van cirrose. Klinisch relevante ascites wordt gedefinieerd als ascites die het gevolg zijn van cirrose en die voortdurende behandeling met diuretica en/of paracentese vereist.
- Urine-eiwit is minder dan of gelijk aan 1+ op peilstok of routine urineonderzoek. Als urine-peilstok of routine-analyse proteïnurie groter dan of gelijk aan 2+ aangeeft, moet 24 uur per dag urine worden verzameld en moet minder dan 1000 milligram (mg) eiwit worden aangetoond.
- Deelnemers met reproductief potentieel (beide geslachten) moeten ermee instemmen om een betrouwbare anticonceptiemethode (hormonale of barrièremethoden) te gebruiken tijdens de onderzoeksperiode en ten minste 12 weken na de laatste dosis studietherapie
- Levensverwachting van meer dan of gelijk aan 3 maanden
- Voorafgaande bestraling is toegestaan indien: Bij thoraxbestraling minimaal 28 dagen zijn verstreken na voltooiing van de bestraling voorafgaand aan randomisatie; Bij focale of palliatieve bestraling zijn minimaal 7 dagen verstreken sinds de laatste bestraling voorafgaand aan randomisatie (en mits 25% of minder van het totale beenmerg is bestraald); In het geval van bestraling van het centrale zenuwstelsel (CZS) zijn ten minste 14 dagen verstreken vanaf de voltooiing van de bestralingsbehandeling voorafgaand aan randomisatie
Uitsluitingscriteria:
- Ziekteprogressie bij meer dan 1 eerdere chemotherapieregimes
- Deelnemers van wie de enige eerdere behandeling een tyrosinekinaseremmer was
- De tumor van de deelnemer bevat geheel of gedeeltelijk kleincellige longkanker
- Grote operatie binnen 28 dagen voorafgaand aan randomisatie, of plaatsing van een hulpmiddel voor subcutane veneuze toegang binnen 7 dagen voorafgaand aan randomisatie. Postoperatieve bloedingscomplicaties of wondcomplicaties van een chirurgische ingreep die in de afgelopen 2 maanden is uitgevoerd.
- Gelijktijdige behandeling met andere antikankertherapie, waaronder andere chemotherapie, immunotherapie, hormonale therapie, chemo-embolisatie of gerichte therapie
- De laatste dosis bevacizumab moet ten minste 28 dagen na randomisatie zijn
- De laatste dosis cytotoxische chemotherapie moet ten minste 14 dagen na randomisatie zijn
- De deelnemer heeft onbehandelde CZS-metastasen. Deelnemers met behandelde hersenmetastasen komen in aanmerking als ze klinisch stabiel zijn met betrekking tot de neurologische functie, zonder steroïden na craniale bestraling die ten minste 2 weken voorafgaand aan randomisatie is geëindigd, of na chirurgische resectie die ten minste 28 dagen voorafgaand aan randomisatie is uitgevoerd. Geen bewijs van Graad groter dan of gelijk aan 1 CZS-bloeding op basis van voorbehandeling Magnetic Resonance Imaging (MRI) of IV-contrast Computertomografie (CT)-scan.
- Radiologisch gedocumenteerd bewijs van een grote invasie of omhulling van bloedvaten door kanker
- Radiografisch bewijs van intratumorcavitatie
- Geschiedenis van ongecontroleerde erfelijke of verworven trombotische aandoening
- Chronische therapie met niet-steroïde anti-inflammatoire geneesmiddelen (NSAID's) of andere plaatjesaggregatieremmers; Aspirinegebruik in doseringen tot 325 milligram per dag (mg/dag) is toegestaan
- Geschiedenis van grove bloedspuwing (gedefinieerd als helder rood bloed of groter dan of gelijk aan 1/2 theelepel) binnen 2 maanden voorafgaand aan randomisatie
- Klinisch relevant congestief hartfalen [New York Heart Association (NYHA II-IV)] of symptomatische of slecht gecontroleerde hartritmestoornissen
- Elke arteriële trombotische gebeurtenis, inclusief myocardinfarct, onstabiele angina, cerebrovasculair accident of voorbijgaande ischemische aanval, binnen 6 maanden voorafgaand aan randomisatie
- Ongecontroleerde arteriële hypertensie groter dan of gelijk aan 150 / groter dan of gelijk aan 90 millimeter kwik (mm Hg) ondanks standaard medische behandeling
- Ernstige of niet-genezende wond, zweer of botbreuk binnen 28 dagen voorafgaand aan randomisatie
- Significante bloedingsstoornissen, vasculitis of Graad 3/4 gastro-intestinale bloeding binnen 3 maanden voorafgaand aan randomisatie
- Gastro-intestinale (GI) perforatie en/of fistels binnen 6 maanden voorafgaand aan randomisatie
- Darmobstructie, voorgeschiedenis of aanwezigheid van inflammatoire enteropathie of uitgebreide darmresectie Ziekte van Crohn, colitis ulcerosa of chronische diarree
- Perifere neuropathie hoger dan of gelijk aan graad 2 [National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) versie 4.02]
- Ernstige ziekte of medische aandoening(en), waaronder, maar niet beperkt tot: infectie met het humaan immunodeficiëntievirus (hiv) of aan het verworven immunodeficiëntiesyndroom (aids) gerelateerde ziekte; Actieve of ongecontroleerde klinisch ernstige infectie; Ernstige acute of chronische medische of psychiatrische aandoening of laboratoriumafwijking die het risico kan verhogen dat gepaard gaat met deelname aan de studie of toediening van onderzoeksmedicatie
- Bekende allergie of overgevoeligheidsreactie op een van de behandelingscomponenten
- De deelnemer is zwanger of geeft borstvoeding
- Huidige of recente (binnen 28 dagen voorafgaand aan randomisatie) behandeling met een onderzoeksgeneesmiddel of apparaat dat op het moment van randomisatie geen wettelijke goedkeuring heeft gekregen voor enige indicatie, of deelname aan een ander interventioneel klinisch onderzoek
- Voorafgaande therapie met docetaxel
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Ramucirumab + Docetaxel
|
10 milligram per kilogram (mg/kg) intraveneus toegediend (IV) op dag 1 van de cyclus van 21 dagen totdat aan ziekteprogressie, onaanvaardbare toxiciteit of een ander ontwenningscriterium is voldaan
Andere namen:
75 milligram per vierkante meter (mg/m^2) (60 mg/m^2 voor de landen Korea en Taiwan alleen met protocolwijziging van 22 mei 2012) intraveneus toegediend op dag 1 van de cyclus van 21 dagen tot ziekteprogressie, onaanvaardbaar toxiciteit of aan een ander ontwenningscriterium is voldaan
|
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Placebo-vergelijker: Placebo + Docetaxel
|
75 milligram per vierkante meter (mg/m^2) (60 mg/m^2 voor de landen Korea en Taiwan alleen met protocolwijziging van 22 mei 2012) intraveneus toegediend op dag 1 van de cyclus van 21 dagen tot ziekteprogressie, onaanvaardbaar toxiciteit of aan een ander ontwenningscriterium is voldaan
IV toegediend op dag 1 van de 21-daagse cyclus totdat aan ziekteprogressie, onaanvaardbare toxiciteit of een ander ontwenningscriterium is voldaan
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Algemeen overleven
Tijdsspanne: Randomisatie tot datum van overlijden door welke oorzaak dan ook (tot 34 maanden)
|
De totale overleving was de tijd vanaf randomisatie tot de datum van overlijden door welke oorzaak dan ook.
Deelnemers die aan het einde van de follow-upperiode in leven waren (of verloren voor de follow-up) werden gecensureerd op de laatste datum waarvan bekend was dat de deelnemer in leven was.
|
Randomisatie tot datum van overlijden door welke oorzaak dan ook (tot 34 maanden)
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Progressievrije overlevingstijd (PFS).
Tijdsspanne: Randomisatie naar gemeten PD of datum van overlijden door welke oorzaak dan ook (tot 29 maanden)
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PFS-tijd was de tijd vanaf randomisatie tot de datum van objectief bepaalde progressieve ziekte (PD) of overlijden door welke oorzaak dan ook, afhankelijk van wat zich het eerst voordeed.
Volgens Response Evaluation Criteria in Solid Tumors versie 1.1 (RECIST v1.1), was PD een toename van ten minste 20% in de som van de diameters van doellaesies, waarbij de kleinste som van het onderzoek als referentie werd genomen.
Naast de relatieve toename van 20% moet de som ook een absolute toename van minimaal 5 millimeter (mm) hebben aangetoond.
Het verschijnen van 1 of meer nieuwe laesies en/of duidelijke progressie van bestaande niet-doellaesies werd ook als progressie beschouwd.
Deelnemers zonder objectief bepaalde PD die aan het einde van de follow-up-periode in leven waren (of verloren voor follow-up) werden gecensureerd op de datum van de laatste volledige radiografische tumorbeoordeling van de deelnemer; als er geen basislijn of post-basislijn radiologische beoordeling beschikbaar was, werd de deelnemer gecensureerd op de datum van randomisatie.
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Randomisatie naar gemeten PD of datum van overlijden door welke oorzaak dan ook (tot 29 maanden)
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Percentage deelnemers dat een objectieve respons behaalt (objectieve responsratio)
Tijdsspanne: Basislijn tot gemeten PD (tot 29 maanden)
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Deelnemers bereikten een objectieve respons als ze als beste algehele respons partiële respons (PR) of complete respons (CR) hadden.
Volgens RECIST v1.1 werd PR gedefinieerd als een afname van ten minste 30% in de som van de diameters van doellaesies (inclusief de korte assen van elke doellymfeknoop), waarbij de basissomdiameter als referentie werd genomen; CR was het verdwijnen van alle niet-nodale doellaesies, met de korte assen van elke doellymfeknoop teruggebracht tot <10 mm, het verdwijnen van alle niet-doellaesies en de normalisatie van tumormarkerniveaus [als tumormarkers aanvankelijk boven de bovenste limiet van normaal (ULN)].
Het percentage deelnemers dat een objectieve respons behaalde=(aantal deelnemers met CR of PR)/(aantal beoordeelde deelnemers)*100.
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Basislijn tot gemeten PD (tot 29 maanden)
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Percentage deelnemers dat ziektebestrijding bereikt (ziektebestrijdingspercentage)
Tijdsspanne: Basislijn tot gemeten PD (tot 29 maanden)
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Deelnemers bereikten ziektecontrole als ze de beste algehele respons hadden van PR, CR of stabiele ziekte (SD).
Volgens RECIST v1.1 werd PR gedefinieerd als een afname van ten minste 30% in de som van de diameters van doellaesies (inclusief de korte assen van elke doellymfeknoop), waarbij de basissomdiameter als referentie werd genomen; CR was het verdwijnen van alle niet-nodale doellaesies, met de korte assen van elke doellymfklier teruggebracht tot <10 mm, het verdwijnen van alle niet-doellaesies en de normalisatie van tumormarkerniveaus (als tumormarkers aanvankelijk boven de ULN waren ).
SD was niet voldoende krimp om als PR te kwalificeren, noch voldoende toename om als PD te kwalificeren, uitgaande van de kleinste totale diameter sinds de start van de behandeling.
Het percentage deelnemers dat ziektebestrijding heeft bereikt=(aantal deelnemers met CR, PR of SD)/(aantal beoordeelde deelnemers)*100.
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Basislijn tot gemeten PD (tot 29 maanden)
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Maximale verbetering op de longkankersymptoomschaal (LCSS)
Tijdsspanne: Basislijn, dag 21 van elke cyclus en 30 dagen na de laatste infusie (tot cyclus 38, 21 dagen/cyclus)
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De LCSS bestond uit 9 items: 6 items waren gericht op longkankersymptomen [verlies van eetlust, vermoeidheid, hoesten, dyspnoe (kortademigheid), bloedspuwing (bloed in sputum) en pijn] en 3 items waren globale items (symptoomangst, interferentie met activiteitenniveau en globale levenskwaliteit).
De reacties van deelnemers op elk item werden gemeten met behulp van visuele analoge schalen (VAS) met lijnen van 100 mm.
Een hogere score voor elk item vertegenwoordigde een hoger niveau van symptomen/problemen.
De Average Symptom Burden Index (ASBI) was het gemiddelde van de 6 symptoomitems van de LCSS en de Total LCSS was het gemiddelde van alle 9 LCSS-items.
ASBI en Total LCSS werden niet berekend voor een deelnemer als hij/zij 1 of meer ontbrekende waarden had voor respectievelijk de 6 en 9 items.
Maximale verbetering in LCSS-scores, ASBI en totale LCSS-score was de grootste afname ten opzichte van de basislijn voor elke variabele, wat de kleinste (meest negatieve of kleinste positieve) niet-ontbrekende waarde was van alle verandering ten opzichte van de basislijnwaarden voor elke variabele.
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Basislijn, dag 21 van elke cyclus en 30 dagen na de laatste infusie (tot cyclus 38, 21 dagen/cyclus)
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Verandering van basislijn naar follow-upbezoek van 30 dagen op European Quality of Life Questionnaire-5 Dimension (EQ-5D) Health State Scores
Tijdsspanne: Basislijn, 30 dagen na de laatste infusie (tot cyclus 38, 21 dagen/cyclus)
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De EQ-5D is een quality-of-life instrument dat uit 2 delen bestaat.
In het eerste deel (Health State Index-score) konden deelnemers hun gezondheidstoestand beoordelen op 5 gezondheidsdomeinen: mobiliteit, zelfzorg, gebruikelijke activiteiten, pijn/ongemak en angst/depressie met behulp van een schaal van 1 tot 3 (geen probleem, sommige respectievelijk extreme problemen).
Deze combinaties van attributen werden omgezet in een gewogen Health State Index-score volgens een op de bevolking gebaseerd algoritme in het Verenigd Koninkrijk; de mogelijke waarden voor de Health State Index-score varieerden van -0,59 (ernstige problemen in alle 5 dimensies) tot 1,0 (geen probleem in welke dimensie dan ook).
Het tweede deel van de EQ-5D was een VAS waarmee deelnemers hun huidige gezondheidstoestand konden beoordelen.
Mogelijke EQ-5D VAS-scores varieerden van 0 (slechtst denkbare gezondheidstoestand) tot 100 (best denkbare gezondheidstoestand).
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Basislijn, 30 dagen na de laatste infusie (tot cyclus 38, 21 dagen/cyclus)
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Maximale en minimale serumconcentraties (Cmax en Cmin) van Ramucirumab
Tijdsspanne: Voorafgaand aan infusie en 1 uur na infusie voor 4 en 8 (cycli 3 en 5 met 21 dagen/cyclus)
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Voorafgaand aan infusie en 1 uur na infusie voor 4 en 8 (cycli 3 en 5 met 21 dagen/cyclus)
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Aantal deelnemers met antilichamen tegen Ramucirumab
Tijdsspanne: Baseline, voorafgaand aan infusie voor week 4 en 8 (cycli 3 en 5), en 30 dagen na laatste infusie (tot cyclus 38, 21 dagen/cyclus)
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Het aantal deelnemers dat tijdens de behandeling of tijdens de follow-up optredende anti-drug-antilichamen (ADA) had, wordt gerapporteerd.
Deelnemers met tijdens de behandeling optredende ADA werden gedefinieerd als deelnemers die vanaf baseline tot en met cyclus 5 pre-infusie een monster hadden dat een 4-voudige toename (2 verdunningstoename) was in immunogeniciteitstiter ten opzichte van de baselinetiter, of deelnemers die negatief testten bij baseline en positief na baseline (bij een titer van ≥1:20).
Deelnemers met follow-up opkomende ADA werden gedefinieerd als deelnemers die gedurende 30 dagen na de laatste infusie een monster hadden dat een 4-voudige toename was (2 verdunningstoename) in immunogeniciteitstiter ten opzichte van de basislijntiter.
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Baseline, voorafgaand aan infusie voor week 4 en 8 (cycli 3 en 5), en 30 dagen na laatste infusie (tot cyclus 38, 21 dagen/cyclus)
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Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Aantal deelnemers dat tijdens de behandeling optredende bijwerkingen (TEAE's) had of stierf
Tijdsspanne: Eerste infusie tot 30 dagen na laatste infusie (tot cyclus 38, 21 dagen/cyclus)
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De gepresenteerde gegevens zijn het aantal deelnemers dat ten minste 1 TEAE, Graad 3, 4 of 5 TEAE, tijdens de behandeling optredende ernstige bijwerkingen (SAE), TEAE die leidde tot stopzetting van de studiebehandeling (ramucirumab/placebo of docetaxel) en TEAE ervoer leidend tot de dood.
Klinisch significante gebeurtenissen werden gedefinieerd als tijdens de behandeling optredende SAE's en andere niet-ernstige bijwerkingen (AE's), ongeacht de causaliteit.
Een samenvatting van SAE's en andere niet-ernstige AE's, ongeacht de causaliteit, bevindt zich in de module Gerapporteerde ongewenste voorvallen.
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Eerste infusie tot 30 dagen na laatste infusie (tot cyclus 38, 21 dagen/cyclus)
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Medewerkers en onderzoekers
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Publicaties en nuttige links
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Algemene publicaties
- Rolfo C, Hess LM, Jen MH, Peterson P, Li X, Liu H, Lai Y, Sugihara T, Kiiskinen U, Vickers A, Summers Y. External control cohorts for the single-arm LIBRETTO-001 trial of selpercatinib in RET+ non-small-cell lung cancer. ESMO Open. 2022 Aug;7(4):100551. doi: 10.1016/j.esmoop.2022.100551. Epub 2022 Aug 2.
- Garon EB, Scagliotti GV, Gautschi O, Reck M, Thomas M, Iglesias Docampo L, Kalofonos H, Kim JH, Gans S, Brustugun OT, Orlov SV, Cuyun Carter G, Zimmermann AH, Oton AB, Alexandris E, Lee P, Wolff K, Stefaniak VJ, Socinski MA, Perol M. Exploratory analysis of front-line therapies in REVEL: a randomised phase 3 study of ramucirumab plus docetaxel versus docetaxel for the treatment of stage IV non-small-cell lung cancer after disease progression on platinum-based therapy. ESMO Open. 2020 Jan;5(1):e000567. doi: 10.1136/esmoopen-2019-000567.
- Garon EB, Ciuleanu TE, Arrieta O, Prabhash K, Syrigos KN, Goksel T, Park K, Gorbunova V, Kowalyszyn RD, Pikiel J, Czyzewicz G, Orlov SV, Lewanski CR, Thomas M, Bidoli P, Dakhil S, Gans S, Kim JH, Grigorescu A, Karaseva N, Reck M, Cappuzzo F, Alexandris E, Sashegyi A, Yurasov S, Perol M. Ramucirumab plus docetaxel versus placebo plus docetaxel for second-line treatment of stage IV non-small-cell lung cancer after disease progression on platinum-based therapy (REVEL): a multicentre, double-blind, randomised phase 3 trial. Lancet. 2014 Aug 23;384(9944):665-73. doi: 10.1016/S0140-6736(14)60845-X. Epub 2014 Jun 2.
- Garon EB, Cao D, Alexandris E, John WJ, Yurasov S, Perol M. A randomized, double-blind, phase III study of Docetaxel and Ramucirumab versus Docetaxel and placebo in the treatment of stage IV non-small-cell lung cancer after disease progression after 1 previous platinum-based therapy (REVEL): treatment rationale and study design. Clin Lung Cancer. 2012 Nov;13(6):505-9. doi: 10.1016/j.cllc.2012.06.007. Epub 2012 Jul 31.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 december 2010
Primaire voltooiing (Werkelijk)
1 december 2013
Studie voltooiing (Werkelijk)
1 augustus 2016
Studieregistratiedata
Eerst ingediend
16 juli 2010
Eerst ingediend dat voldeed aan de QC-criteria
22 juli 2010
Eerst geplaatst (Schatting)
23 juli 2010
Updates van studierecords
Laatste update geplaatst (Werkelijk)
25 september 2019
Laatste update ingediend die voldeed aan QC-criteria
10 september 2019
Laatst geverifieerd
1 september 2019
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Ziekten van de luchtwegen
- Neoplasmata
- Longziekten
- Neoplasmata per site
- Neoplasmata van de luchtwegen
- Thoracale neoplasmata
- Carcinoom, bronchogeen
- Bronchiale neoplasmata
- Longneoplasmata
- Carcinoom, niet-kleincellige long
- Fysiologische effecten van medicijnen
- Moleculaire mechanismen van farmacologische werking
- Antineoplastische middelen
- Immunologische factoren
- Tubuline-modulatoren
- Antimitotische middelen
- Mitose modulatoren
- Docetaxel
- Ramucirumab
- Antilichamen, monoklonaal
Andere studie-ID-nummers
- 13852
- I4T-MC-JVBA (Andere identificatie: Eli Lilly and Company)
- 2010-021297-11 (EudraCT-nummer)
- CP12-1027 (Andere identificatie: ImClone Trial Number)
- CTRI/2011/08/001942 (Register-ID: Clinical Trials Registry India)
Plan Individuele Deelnemersgegevens (IPD)
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Beschrijving IPD-plan
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IPD-tijdsbestek voor delen
Gegevens zijn beschikbaar 6 maanden na de primaire publicatie en goedkeuring van de onderzochte indicatie in de VS en de EU, afhankelijk van wat later is.
Gegevens zullen voor onbepaalde tijd beschikbaar zijn om op te vragen.
IPD-toegangscriteria voor delen
Een onderzoeksvoorstel moet worden goedgekeurd door een onafhankelijk beoordelingspanel en onderzoekers moeten een overeenkomst voor het delen van gegevens ondertekenen.
IPD delen Ondersteunend informatietype
- LEERPROTOCOOL
- SAP
- MVO
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .