- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01870284
Undersøgelse af Ixekizumab hos deltagere med aktiv ankyloserende spondylitis (AS) (SPIRIT A1)
15. september 2014 opdateret af: Eli Lilly and Company
En multicenter, randomiseret, dobbeltblind, aktiv og placebokontrolleret 16-ugers undersøgelse efterfulgt af langtidsevaluering af Ixekizumabs effekt og sikkerhed (LY2439821) hos patienter med aktiv ankyloserende spondylitis
Denne undersøgelse vil vurdere sikkerheden og effekten af ixekizumab (LY2439821) sammenlignet med placebo hos deltagere med aktiv AS.
Studieoversigt
Status
Trukket tilbage
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Fase
- Fase 3
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Buenos Aires, Argentina, C1428DQG
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Caba, Argentina, 1181
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Córdoba, Argentina, X5004BAL
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San Miguel De Tucuman, Argentina, T4000AXL
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Genk, Belgien, 3600
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Gent, Belgien, 9000
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Liège, Belgien, 4000
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Mons, Belgien, 7000
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Alberta
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Edmonton, Alberta, Canada, T6G 2R7
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Manitoba
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Winnipeg, Manitoba, Canada, R3N 0K6
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Ontario
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Toronto, Ontario, Canada, M5T 2S8
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Quebec
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Quebec City, Quebec, Canada, G1W 4R4
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Rimouski, Quebec, Canada, G5L 8W1
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Sainte-Foy, Quebec, Canada, G1V 3M7
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Barnaul, Den Russiske Føderation, 656024
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Ekaterinburg, Den Russiske Føderation, 620102
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Kazan, Den Russiske Føderation, 420097
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Krasnoyarsk, Den Russiske Føderation, 660022
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Moscow, Den Russiske Føderation
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Novosibirsk, Den Russiske Føderation, 630099
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Petrozavodsk, Den Russiske Føderation, 185019
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Ryazan, Den Russiske Føderation, 390026
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Saint Petersburg, Den Russiske Føderation, 194291
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Greater London
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London, Greater London, Det Forenede Kongerige, E11 1NR
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Hants
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Southampton, Hants, Det Forenede Kongerige, SO16 6YD
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Norfolk
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Norwich, Norfolk, Det Forenede Kongerige, NR4 7UY
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West Midlands
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Coventry, West Midlands, Det Forenede Kongerige, CV2 2DX
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Wolverhampton, West Midlands, Det Forenede Kongerige, WV10 0QP
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West Yorkshire
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Bradford, West Yorkshire, Det Forenede Kongerige, BD5 0NA
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Leeds, West Yorkshire, Det Forenede Kongerige, LS7 4SA
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Alabama
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Birmingham, Alabama, Forenede Stater, 35205
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Arkansas
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Little Rock, Arkansas, Forenede Stater, 72205
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California
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Upland, California, Forenede Stater, 91786
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Colorado
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Denver, Colorado, Forenede Stater, 80230
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Connecticut
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Trumbull, Connecticut, Forenede Stater, 06611
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Florida
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Tampa, Florida, Forenede Stater, 33609
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Georgia
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Atlanta, Georgia, Forenede Stater, 30342
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Decatur, Georgia, Forenede Stater, 30033
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Marietta, Georgia, Forenede Stater, 30060
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Idaho
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Boise, Idaho, Forenede Stater, 83704
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Idaho Falls, Idaho, Forenede Stater, 83404
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Iowa
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Cedar Rapids, Iowa, Forenede Stater, 52401
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Kansas
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Wichita, Kansas, Forenede Stater, 67207
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Maryland
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Cumberland, Maryland, Forenede Stater, 21502
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Hagerstown, Maryland, Forenede Stater, 21740
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Massachusetts
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Worcester, Massachusetts, Forenede Stater, 01605
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Michigan
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Ann Arbor, Michigan, Forenede Stater, 48109
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New York
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Albany, New York, Forenede Stater, 12206
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Brooklyn, New York, Forenede Stater, 11201
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Mineola, New York, Forenede Stater, 11501
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North Carolina
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Asheville, North Carolina, Forenede Stater, 28803
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Charlotte, North Carolina, Forenede Stater, 28210
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Ohio
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Toledo, Ohio, Forenede Stater, 43606
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Oregon
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Lake Oswego, Oregon, Forenede Stater, 97035
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Portland, Oregon, Forenede Stater, 97239
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South Carolina
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Charleston, South Carolina, Forenede Stater, 29407
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Columbia, South Carolina, Forenede Stater, 29204
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North Charleston, South Carolina, Forenede Stater, 29406
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Tennessee
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Hixon, Tennessee, Forenede Stater, 37343
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Jackson, Tennessee, Forenede Stater, 38305
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Texas
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Dallas, Texas, Forenede Stater, 75231
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Houston, Texas, Forenede Stater, 77036
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Washington
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Kennewick, Washington, Forenede Stater, 99336
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Seattle, Washington, Forenede Stater, 98104
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Amiens, Frankrig, 80054
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Bordeaux, Frankrig, 33076
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Montpellier, Frankrig, 34295
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Nantes, Frankrig, 44093
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Orleans, Frankrig, 45032
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Paris, Frankrig, 75679
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Rennes, Frankrig, 35202
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Strasbourg, Frankrig, 67098
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Amsterdam, Holland, 1105 AZ
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Breda, Holland, 4818 CK
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Leiden, Holland, 2333 ZA
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Maastricht, Holland, 6229 HX
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Nijmegen, Holland, 6522 JV
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Rotterdam, Holland, 3079 DZ
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Sneek, Holland, 8601 ZK
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Guadalajara, Mexico, 45040
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Mexico City, Mexico, 06700
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Monterrey, Mexico, 64000
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Morelia, Mexico, 58249
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San Luis, Mexico, 78200
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Katowice, Polen, 40-635
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Krakow, Polen, 31-501
- 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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Lublin, Polen, 20582
- 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, 60-539
- 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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Warsaw, Polen, 02-118
- 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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Wroclaw, Polen, 51-124
- 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, Spanien, 08034
- 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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Bilbao, Spanien, 48013
- 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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Cordoba, Spanien, 14004
- 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 Coruña, Spanien, 15006
- 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, Spanien, 28007
- 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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Málaga, Spanien, 29009
- 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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Oviedo, Spanien, 33012
- 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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Santander, Spanien, 39008
- 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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Sevilla, Spanien, 41009
- 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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Brno, Tjekkiet, 638 00
- 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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Bruntal, Tjekkiet, 79201
- 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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Kladno, Tjekkiet, 272 01
- 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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Ostrava - Trebovice, Tjekkiet, 722 00
- 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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Prague, Tjekkiet, 140 00
- 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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Zlin, Tjekkiet, 760 01
- 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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Bad Doberan, Tyskland, 18209
- 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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Berlin, Tyskland, 12203
- 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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Halle, Tyskland, 06108
- 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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Heidelberg, Tyskland, 69121
- 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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Ratingen, Tyskland, 40882
- 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, Ukraine, 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, Ukraine, 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, Ukraine, 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, Ukraine, 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, Ukraine, 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, Ukraine, 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, Ukraine, 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, Ukraine, 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, Ukraine, 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, Ukraine, 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, Ungarn, 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, Ungarn, 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, Ungarn, 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, Ungarn, 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, Ungarn, 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, Ungarn, 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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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inklusionskriterier:
- Diagnose af moderat til svær AS med forudgående dokumenteret radiologisk evidens (røntgen), der opfylder de modificerede New York-kriterier for AS (1984)
- Har aktiv AS defineret som Bath Ankyloserende Spondylitis Disease Activity Index (BASDAI) ≥4 og spinal smerte (rygsmerter) score ≥4 på en numerisk vurderingsskala (NRS)
- Deltagerne skulle have været på ikke-steroide antiinflammatoriske lægemidler (NSAID'er) med en utilstrækkelig respons
- Deltagere, der regelmæssigt tager NSAID'er eller cyclooxygenase-2 (COX-2)-hæmmere som en del af deres AS-behandling, skal have en stabil dosis
- Deltagere, der har været på en tumor nekrose faktor alfa (TNF) hæmmer (ikke mere end én) skal have oplevet en utilstrækkelig respons
- Samlet varighed af tidligere behandling (NSAID'er og/eller tilstrækkelig fysioterapi) bør være mindst 12 uger
- Mænd skal acceptere at bruge en pålidelig præventionsmetode eller forblive afholdende under undersøgelsen
- Kvinder skal acceptere at bruge pålidelig prævention eller forblive afholdende under undersøgelsen og i mindst 12 uger efter ophør af behandlingen
Ekskluderingskriterier:
- Deltagere med total ankylose i rygsøjlen
- Tidligere eller nuværende behandling med adalimumab
- Deltagere tidligere behandlet med et hvilket som helst biologisk eller andet immunmodulerende middel bortset fra dem, der er målrettet mod TNF
- Beviser for aktive inflammatoriske arthritiske syndromer eller spondyloarthropatier bortset fra ankyloserende spondylitis
- Har deltaget i et hvilket som helst studie med interleukin 17 (IL-17) antagonister, inklusive ixekizumab
- Alvorlig lidelse eller anden sygdom end ankyloserende spondylitis
- Alvorlig infektion inden for de sidste 3 måneder
- Ammende eller ammende (ammende) kvinder
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Ixekizumab doseringsregime 1
Administreret ved 80 milligram (mg) subkutan (SC) injektion
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Administreret SC
Andre navne:
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Eksperimentel: Ixekizumab doseringsregime 2
Administreret ved 80 mg SC-injektion
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Administreret SC
Andre navne:
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Placebo komparator: Placebo
Placebo for ixekizumab og placebo for adalimumab administreret ved subkutan injektion
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Administreret SC
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Aktiv komparator: Adalimumab
Administreret ved 40 mg SC-injektion
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Administreret SC
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Effekten af Ixekizumab hos deltagere med ankyloserende spondylitis (AS). Foranstaltning: Vurdering af SpondyloArthritis International Society Criteria (ASAS20)
Tidsramme: 16 uger
|
16 uger
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Effekten af Ixekizumab hos deltagere med AS. Mål: ASAS
Tidsramme: 16 uger
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16 uger
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Livskvalitet og resultatvurderinger. Mål: Patientrapporterede resultater (PRO)
Tidsramme: Baseline gennem 16 uger
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Baseline gennem 16 uger
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Effekten af Ixekizumab hos deltagere med AS. Foranstaltning: Ikke-gigtsygdomsvurderinger
Tidsramme: Baseline gennem 16 uger
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Baseline gennem 16 uger
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Effekten af Ixekizumab hos deltagere med AS. Mål: Perifere led tæller
Tidsramme: 16 uger
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16 uger
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Effekten af Ixekizumab hos deltagere med AS. Mål: Spinal mobilitet
Tidsramme: Baseline gennem 16 uger
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Baseline gennem 16 uger
|
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Effekten af Ixekizumab hos deltagere med AS. Mål: modificeret Stoke Ankyloserende Spondylitis Spinal Score (mSASSS)
Tidsramme: Baseline gennem 108 uger
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Baseline gennem 108 uger
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. juli 2014
Primær færdiggørelse (Forventet)
1. april 2016
Studieafslutning (Forventet)
1. april 2018
Datoer for studieregistrering
Først indsendt
3. juni 2013
Først indsendt, der opfyldte QC-kriterier
3. juni 2013
Først opslået (Skøn)
6. juni 2013
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
16. september 2014
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
15. september 2014
Sidst verificeret
1. september 2014
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 13650
- I1F-MC-RHAO (Anden identifikator: Eli Lilly and Company)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Spondylitis, ankyloserende
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Eighth Affiliated Hospital, Sun Yat-sen UniversityGuangzhou Cellgenes Biotechnology Co.,LtdIkke rekrutterer endnuAnkyloserende spondylitisKina
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Sohag UniversityIkke rekrutterer endnuAnkyloserende spondylitis
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Saglik Bilimleri UniversitesiRekrutteringAnkyloserende spondylitisTyrkiet (Türkiye)
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Henan Provincial People's HospitalThe Second Affiliated Hospital of Henan University of Traditional Chinese...Trukket tilbageAnkyloserende spondylitisKina
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SPH-BIOCAD (HK) LimitedAfsluttet
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China-Japan Friendship HospitalThe Second Affiliated Hospital of Henan University of Traditional Chinese...Rekruttering
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Shenzhen Huishan Biotechnology Co., Ltd.Southern Medical University, ChinaIkke rekrutterer endnu
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Lynk Pharmaceuticals Co., LtdRekrutteringAnkyloserende spondylitisKina
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Bursa City HospitalAfsluttetAnklyoserende spondylitisTyrkiet (Türkiye)
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Sunshine Guojian Pharmaceutical (Shanghai) Co.,...RekrutteringAnkyloserende spondylitisKina
Kliniske forsøg med Ixekizumab
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Shanghai Yueyang Integrated Medicine HospitalShanghai Skin Disease and Venereal Disease HospitalIkke rekrutterer endnu
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Eli Lilly and CompanyAfsluttetPlaque PsoriasisForenede Stater, Puerto Rico
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CelltrionAktiv, ikke rekrutterende
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University of New MexicoAfsluttetLav Planus | Lichen Planopilaris | Lichen Planus HovedbundForenede Stater
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Massachusetts Eye Research and Surgery InstitutionEli Lilly and CompanyRekrutteringUveitis, Anterior | Panuveitis | Uveitis, posterior | Uveitis, mellemliggendeForenede Stater
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Eli Lilly and CompanyAfsluttet
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Eli Lilly and CompanyAfsluttetPsoriasisgigtForenede Stater, Frankrig, Taiwan, Spanien, Australien, Tyskland, Det Forenede Kongerige, Polen, Tjekkiet, Italien
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Eli Lilly and CompanyAfsluttetRheumatoid arthritisTyskland, Forenede Stater, Rumænien, Den Russiske Føderation, Argentina, Peru, Polen, Taiwan, Korea, Republikken, Indien, Chile
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Eli Lilly and CompanyAfsluttetPsoriasisItalien, Forenede Stater, Australien, Tyskland, Canada, Danmark, Japan, Polen, Ungarn, Rumænien, Det Forenede Kongerige
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Icahn School of Medicine at Mount SinaiAfsluttet