- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT01870284
Badanie iksekizumabu u uczestników z czynnym zesztywniającym zapaleniem stawów kręgosłupa (ZZSK) (SPIRIT A1)
15 września 2014 zaktualizowane przez: Eli Lilly and Company
Wieloośrodkowe, randomizowane, podwójnie ślepe, aktywne i kontrolowane placebo badanie trwające 16 tygodni, po którym następowała długoterminowa ocena skuteczności i bezpieczeństwa iksekizumabu (LY2439821) u pacjentów z czynnym zesztywniającym zapaleniem stawów kręgosłupa
Badanie to oceni bezpieczeństwo i skuteczność iksekizumabu (LY2439821) w porównaniu z placebo u uczestników z aktywnym AS.
Przegląd badań
Status
Wycofane
Interwencja / Leczenie
Typ studiów
Interwencyjne
Faza
- Faza 3
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
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Buenos Aires, Argentyna, C1428DQG
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Caba, Argentyna, 1181
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Córdoba, Argentyna, X5004BAL
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San Miguel De Tucuman, Argentyna, T4000AXL
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Genk, Belgia, 3600
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Gent, Belgia, 9000
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Liège, Belgia, 4000
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Mons, Belgia, 7000
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Barnaul, Federacja Rosyjska, 656024
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Ekaterinburg, Federacja Rosyjska, 620102
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Kazan, Federacja Rosyjska, 420097
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Krasnoyarsk, Federacja Rosyjska, 660022
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Moscow, Federacja Rosyjska
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Novosibirsk, Federacja Rosyjska, 630099
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Petrozavodsk, Federacja Rosyjska, 185019
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Ryazan, Federacja Rosyjska, 390026
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Saint Petersburg, Federacja Rosyjska, 194291
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Amiens, Francja, 80054
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Bordeaux, Francja, 33076
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Montpellier, Francja, 34295
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Nantes, Francja, 44093
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Orleans, Francja, 45032
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Paris, Francja, 75679
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Rennes, Francja, 35202
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Strasbourg, Francja, 67098
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Barcelona, Hiszpania, 08034
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Bilbao, Hiszpania, 48013
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Cordoba, Hiszpania, 14004
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La Coruña, Hiszpania, 15006
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Madrid, Hiszpania, 28007
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Málaga, Hiszpania, 29009
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Oviedo, Hiszpania, 33012
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Santander, Hiszpania, 39008
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Sevilla, Hiszpania, 41009
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Amsterdam, Holandia, 1105 AZ
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Breda, Holandia, 4818 CK
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Leiden, Holandia, 2333 ZA
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Maastricht, Holandia, 6229 HX
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Nijmegen, Holandia, 6522 JV
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Rotterdam, Holandia, 3079 DZ
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Sneek, Holandia, 8601 ZK
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Alberta
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Edmonton, Alberta, Kanada, T6G 2R7
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Manitoba
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Winnipeg, Manitoba, Kanada, R3N 0K6
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Ontario
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Toronto, Ontario, Kanada, M5T 2S8
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Quebec
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Quebec City, Quebec, Kanada, G1W 4R4
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Rimouski, Quebec, Kanada, G5L 8W1
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Sainte-Foy, Quebec, Kanada, G1V 3M7
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Guadalajara, Meksyk, 45040
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Mexico City, Meksyk, 06700
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Monterrey, Meksyk, 64000
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Morelia, Meksyk, 58249
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San Luis, Meksyk, 78200
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Bad Doberan, Niemcy, 18209
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Berlin, Niemcy, 12203
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Halle, Niemcy, 06108
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Heidelberg, Niemcy, 69121
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Ratingen, Niemcy, 40882
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Katowice, Polska, 40-635
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Krakow, Polska, 31-501
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Lublin, Polska, 20582
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Poznan, Polska, 60-539
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Warsaw, Polska, 02-118
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Wroclaw, Polska, 51-124
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Brno, Republika Czeska, 638 00
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Bruntal, Republika Czeska, 79201
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Kladno, Republika Czeska, 272 01
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Ostrava - Trebovice, Republika Czeska, 722 00
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Prague, Republika Czeska, 140 00
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Zlin, Republika Czeska, 760 01
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Alabama
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Birmingham, Alabama, Stany Zjednoczone, 35205
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Arkansas
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Little Rock, Arkansas, Stany Zjednoczone, 72205
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California
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Upland, California, Stany Zjednoczone, 91786
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Colorado
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Denver, Colorado, Stany Zjednoczone, 80230
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Connecticut
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Trumbull, Connecticut, Stany Zjednoczone, 06611
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Florida
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Tampa, Florida, Stany Zjednoczone, 33609
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Georgia
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Atlanta, Georgia, Stany Zjednoczone, 30342
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Decatur, Georgia, Stany Zjednoczone, 30033
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Marietta, Georgia, Stany Zjednoczone, 30060
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Idaho
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Boise, Idaho, Stany Zjednoczone, 83704
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Idaho Falls, Idaho, Stany Zjednoczone, 83404
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Iowa
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Cedar Rapids, Iowa, Stany Zjednoczone, 52401
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Kansas
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Wichita, Kansas, Stany Zjednoczone, 67207
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Maryland
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Cumberland, Maryland, Stany Zjednoczone, 21502
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Hagerstown, Maryland, Stany Zjednoczone, 21740
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Massachusetts
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Worcester, Massachusetts, Stany Zjednoczone, 01605
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Michigan
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Ann Arbor, Michigan, Stany Zjednoczone, 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.
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New York
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Albany, New York, Stany Zjednoczone, 12206
- 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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Brooklyn, New York, Stany Zjednoczone, 11201
- 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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Mineola, New York, Stany Zjednoczone, 11501
- 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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Asheville, North Carolina, Stany Zjednoczone, 28803
- 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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Charlotte, North Carolina, Stany Zjednoczone, 28210
- 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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Toledo, Ohio, Stany Zjednoczone, 43606
- 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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Oregon
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Lake Oswego, Oregon, Stany Zjednoczone, 97035
- 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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Portland, Oregon, Stany Zjednoczone, 97239
- 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, Stany Zjednoczone, 29407
- 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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Columbia, South Carolina, Stany Zjednoczone, 29204
- 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 Charleston, South Carolina, Stany Zjednoczone, 29406
- 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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Hixon, Tennessee, Stany Zjednoczone, 37343
- 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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Jackson, Tennessee, Stany Zjednoczone, 38305
- 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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Dallas, Texas, Stany Zjednoczone, 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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Houston, Texas, Stany Zjednoczone, 77036
- 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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Kennewick, Washington, Stany Zjednoczone, 99336
- 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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Seattle, Washington, Stany Zjednoczone, 98104
- 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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Dnipropetrovsk, Ukraina, 49044
- 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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Donetsk, Ukraina, 83045
- 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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Ivano-Frankivsk, Ukraina, 76018
- 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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Kharkiv, Ukraina, 61039
- 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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Kyiv, Ukraina, 1601
- 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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Lutsk, Ukraina, 43024
- 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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Odesa, Ukraina, 65026
- 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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Vinnytsia, Ukraina, 21018
- 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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Vinnytsya, Ukraina, 21018
- 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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Zaporizhzhia, Ukraina, 69600
- 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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Balatonfüred, Węgry, 8230
- 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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Budapest, Węgry, 1036
- 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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Debrecen, Węgry, 4032
- 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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Kalocsa, Węgry, H-6300
- 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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Nyiregyhaza, Węgry, 4400
- 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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Veszprem, Węgry, 8200
- 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, Zjednoczone Królestwo, E11 1NR
- 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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Hants
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Southampton, Hants, Zjednoczone Królestwo, SO16 6YD
- 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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Norfolk
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Norwich, Norfolk, Zjednoczone Królestwo, NR4 7UY
- 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, Zjednoczone Królestwo, 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, Zjednoczone Królestwo, 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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West Yorkshire
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Bradford, West Yorkshire, Zjednoczone Królestwo, BD5 0NA
- 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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Leeds, West Yorkshire, Zjednoczone Królestwo, LS7 4SA
- 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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Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
18 lat i starsze (Dorosły, Starszy dorosły)
Akceptuje zdrowych ochotników
Nie
Płeć kwalifikująca się do nauki
Wszystko
Opis
Kryteria przyjęcia:
- Rozpoznanie umiarkowanego do ciężkiego ZA na podstawie wcześniej udokumentowanych dowodów radiologicznych (zdjęcie rentgenowskie) spełniających zmodyfikowane kryteria nowojorskie dotyczące AS (1984)
- Mieć aktywny AS zdefiniowany jako wskaźnik BASDAI (ang. Bath Ankylosing Spondylitis Disease Activity Index) ≥ 4 i wynik bólu kręgosłupa (ból pleców) ≥ 4 w numerycznej skali oceny (NRS)
- Uczestnicy powinni być na niesteroidowych lekach przeciwzapalnych (NLPZ) z niewystarczającą odpowiedzią
- Uczestnicy, którzy regularnie przyjmują NLPZ lub inhibitory cyklooksygenazy-2 (COX-2) w ramach terapii AS, muszą przyjmować stabilną dawkę
- Uczestnicy, którzy byli na inhibitorze czynnika martwicy nowotworów alfa (TNF) (nie więcej niż jeden), musieli doświadczyć niewystarczającej odpowiedzi
- Całkowity czas trwania wcześniejszej terapii (NLPZ i/lub odpowiednia fizjoterapia) powinien wynosić co najmniej 12 tygodni
- Mężczyźni muszą wyrazić zgodę na stosowanie niezawodnej metody antykoncepcji lub zachować abstynencję podczas badania
- Kobiety muszą wyrazić zgodę na stosowanie niezawodnej antykoncepcji lub zachować abstynencję podczas badania i przez co najmniej 12 tygodni po zakończeniu leczenia
Kryteria wyłączenia:
- Uczestnicy z całkowitym zesztywnieniem kręgosłupa
- Wcześniejsze lub obecne leczenie adalimumabem
- Uczestnicy wcześniej leczeni jakimikolwiek biologicznymi lub innymi czynnikami immunomodulującymi, z wyjątkiem tych ukierunkowanych na TNF
- Dowody na aktywne zespoły zapalne stawów lub spondyloartropatie inne niż zesztywniające zapalenie stawów kręgosłupa
- Brali udział w jakimkolwiek badaniu antagonistów interleukiny 17 (IL-17), w tym iksekizumabu
- Poważne zaburzenie lub choroba inna niż zesztywniające zapalenie stawów kręgosłupa
- Ciężka infekcja w ciągu ostatnich 3 miesięcy
- Kobiety karmiące piersią lub karmiące piersią
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Poczwórny
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Eksperymentalny: Schemat dawkowania iksekizumabu 1
Podawany we wstrzyknięciu podskórnym (SC) 80 miligramów (mg).
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Administrowany SC
Inne nazwy:
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Eksperymentalny: Schemat dawkowania iksekizumabu 2
Podawane przez wstrzyknięcie podskórne 80 mg
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Administrowany SC
Inne nazwy:
|
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Komparator placebo: Placebo
Placebo dla iksekizumabu i placebo dla adalimumabu podawanego we wstrzyknięciu SC
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Administrowany SC
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Aktywny komparator: Adalimumab
Podawany we wstrzyknięciu 40 mg SC
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Administrowany SC
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Ramy czasowe |
|---|---|
|
Skuteczność iksekizumabu u uczestników z zesztywniającym zapaleniem stawów kręgosłupa (ZZSK). Środek: ocena międzynarodowych kryteriów SpondyloArthritis International Society (ASAS20)
Ramy czasowe: 16 tygodni
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16 tygodni
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Miary wyników drugorzędnych
Miara wyniku |
Ramy czasowe |
|---|---|
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Skuteczność iksekizumabu u uczestników z ZA. Środek: ASAS
Ramy czasowe: 16 tygodni
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16 tygodni
|
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Ocena jakości życia i wyników. Środki: wyniki zgłaszane przez pacjentów (PRO)
Ramy czasowe: Linia bazowa do 16 tygodni
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Linia bazowa do 16 tygodni
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Skuteczność iksekizumabu u uczestników z ZA. Środek: oceny chorób niezwiązanych z zapaleniem stawów
Ramy czasowe: Linia bazowa do 16 tygodni
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Linia bazowa do 16 tygodni
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Skuteczność iksekizumabu u uczestników z ZA. Zmierz: liczbę stawów obwodowych
Ramy czasowe: 16 tygodni
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16 tygodni
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Skuteczność iksekizumabu u uczestników z ZA. Miara: Mobilność kręgosłupa
Ramy czasowe: Linia bazowa do 16 tygodni
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Linia bazowa do 16 tygodni
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Skuteczność iksekizumabu u uczestników z ZA. Zmierz: zmodyfikowany wynik Stoke zesztywniającego zapalenia stawów kręgosłupa (mSASSS)
Ramy czasowe: Linia bazowa do 108 tygodni
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Linia bazowa do 108 tygodni
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Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów
1 lipca 2014
Zakończenie podstawowe (Oczekiwany)
1 kwietnia 2016
Ukończenie studiów (Oczekiwany)
1 kwietnia 2018
Daty rejestracji na studia
Pierwszy przesłany
3 czerwca 2013
Pierwszy przesłany, który spełnia kryteria kontroli jakości
3 czerwca 2013
Pierwszy wysłany (Oszacować)
6 czerwca 2013
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
16 września 2014
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
15 września 2014
Ostatnia weryfikacja
1 września 2014
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Infekcje
- Choroby stawów
- Choroby układu mięśniowo-szkieletowego
- Artretyzm
- Choroby kręgosłupa
- Choroby kości
- Spondylartropatie
- Choroby kości, zakaźne
- Ankyloza
- Zapalenie stawów kręgosłupa
- Zapalenie stawów kręgosłupa
- Zapalenie stawów kręgosłupa, zesztywniające
- Środki przeciwzapalne
- Środki przeciwreumatyczne
- Środki dermatologiczne
- Adalimumab
- Iksekizumab
Inne numery identyfikacyjne badania
- 13650
- I1F-MC-RHAO (Inny identyfikator: Eli Lilly and Company)
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .