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Studie van Ixekizumab bij deelnemers met actieve spondylitis ankylopoetica (AS) (SPIRIT A1)

15 september 2014 bijgewerkt door: Eli Lilly and Company

Een multicenter, gerandomiseerde, dubbelblinde, actieve en placebogecontroleerde studie van 16 weken, gevolgd door langetermijnevaluatie van de werkzaamheid en veiligheid van Ixekizumab (LY2439821) bij patiënten met actieve spondylitis ankylopoetica

Deze studie zal de veiligheid en werkzaamheid van ixekizumab (LY2439821) beoordelen in vergelijking met placebo bij deelnemers met actieve AS.

Studie Overzicht

Studietype

Ingrijpend

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

      • Buenos Aires, Argentinië, C1428DQG
        • 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.
      • Caba, Argentinië, 1181
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      • Córdoba, Argentinië, X5004BAL
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      • San Miguel De Tucuman, Argentinië, T4000AXL
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      • Genk, België, 3600
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      • Gent, België, 9000
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      • Liège, België, 4000
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      • Mons, België, 7000
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    • Alberta
      • Edmonton, Alberta, Canada, T6G 2R7
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    • Manitoba
      • Winnipeg, Manitoba, Canada, R3N 0K6
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    • Ontario
      • Toronto, Ontario, Canada, M5T 2S8
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    • Quebec
      • 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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      • Bad Doberan, Duitsland, 18209
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      • Berlin, Duitsland, 12203
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      • Halle, Duitsland, 06108
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      • Heidelberg, Duitsland, 69121
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      • Ratingen, Duitsland, 40882
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      • Amiens, Frankrijk, 80054
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      • Bordeaux, Frankrijk, 33076
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      • Montpellier, Frankrijk, 34295
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      • Nantes, Frankrijk, 44093
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      • Orleans, Frankrijk, 45032
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      • Paris, Frankrijk, 75679
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      • Rennes, Frankrijk, 35202
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      • Strasbourg, Frankrijk, 67098
        • 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.
      • Balatonfüred, Hongarije, 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.
      • Budapest, Hongarije, 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.
      • Debrecen, Hongarije, 4032
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      • Kalocsa, Hongarije, 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.
      • Nyiregyhaza, Hongarije, 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.
      • Veszprem, Hongarije, 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.
      • Guadalajara, Mexico, 45040
        • 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.
      • Mexico City, Mexico, 06700
        • 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.
      • Monterrey, Mexico, 64000
        • 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.
      • Morelia, Mexico, 58249
        • 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.
      • San Luis, Mexico, 78200
        • 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.
      • Amsterdam, Nederland, 1105 AZ
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      • Breda, Nederland, 4818 CK
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      • Leiden, Nederland, 2333 ZA
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      • Maastricht, Nederland, 6229 HX
        • 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.
      • Nijmegen, Nederland, 6522 JV
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      • Rotterdam, Nederland, 3079 DZ
        • 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.
      • Sneek, Nederland, 8601 ZK
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      • Dnipropetrovsk, Oekraïne, 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.
      • Donetsk, Oekraïne, 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.
      • Ivano-Frankivsk, Oekraïne, 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.
      • Kharkiv, Oekraïne, 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.
      • Kyiv, Oekraïne, 1601
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      • Lutsk, Oekraïne, 43024
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      • Odesa, Oekraïne, 65026
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      • Vinnytsia, Oekraïne, 21018
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      • Vinnytsya, Oekraïne, 21018
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      • Zaporizhzhia, Oekraïne, 69600
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      • Katowice, Polen, 40-635
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      • Krakow, Polen, 31-501
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      • Lublin, Polen, 20582
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      • Poznan, Polen, 60-539
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      • Warsaw, Polen, 02-118
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      • Wroclaw, Polen, 51-124
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      • Barnaul, Russische Federatie, 656024
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      • Ekaterinburg, Russische Federatie, 620102
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      • Kazan, Russische Federatie, 420097
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      • Krasnoyarsk, Russische Federatie, 660022
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      • Moscow, Russische Federatie
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      • Novosibirsk, Russische Federatie, 630099
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      • Petrozavodsk, Russische Federatie, 185019
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      • Ryazan, Russische Federatie, 390026
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      • Saint Petersburg, Russische Federatie, 194291
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      • Barcelona, Spanje, 08034
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      • Bilbao, Spanje, 48013
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      • Cordoba, Spanje, 14004
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      • La Coruña, Spanje, 15006
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      • Madrid, Spanje, 28007
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      • Málaga, Spanje, 29009
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      • Oviedo, Spanje, 33012
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      • Santander, Spanje, 39008
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      • Sevilla, Spanje, 41009
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      • Brno, Tsjechische Republiek, 638 00
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      • Bruntal, Tsjechische Republiek, 79201
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      • Kladno, Tsjechische Republiek, 272 01
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      • Ostrava - Trebovice, Tsjechische Republiek, 722 00
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      • Prague, Tsjechische Republiek, 140 00
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      • Zlin, Tsjechische Republiek, 760 01
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    • Greater London
      • London, Greater London, Verenigd Koninkrijk, E11 1NR
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    • Hants
      • Southampton, Hants, Verenigd Koninkrijk, SO16 6YD
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    • Norfolk
      • Norwich, Norfolk, Verenigd Koninkrijk, NR4 7UY
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    • West Midlands
      • Coventry, West Midlands, Verenigd Koninkrijk, CV2 2DX
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      • Wolverhampton, West Midlands, Verenigd Koninkrijk, WV10 0QP
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    • West Yorkshire
      • Bradford, West Yorkshire, Verenigd Koninkrijk, 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.
      • Leeds, West Yorkshire, Verenigd Koninkrijk, 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.
    • Alabama
      • Birmingham, Alabama, Verenigde Staten, 35205
        • 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.
    • Arkansas
      • Little Rock, Arkansas, Verenigde Staten, 72205
        • 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.
    • California
      • Upland, California, Verenigde Staten, 91786
        • 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.
    • Colorado
      • Denver, Colorado, Verenigde Staten, 80230
        • 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.
    • Connecticut
      • Trumbull, Connecticut, Verenigde Staten, 06611
        • 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.
    • Florida
      • Tampa, Florida, Verenigde Staten, 33609
        • 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.
    • Georgia
      • Atlanta, Georgia, Verenigde Staten, 30342
        • 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.
      • Decatur, Georgia, Verenigde Staten, 30033
        • 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.
      • Marietta, Georgia, Verenigde Staten, 30060
        • 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.
    • Idaho
      • Boise, Idaho, Verenigde Staten, 83704
        • 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.
      • Idaho Falls, Idaho, Verenigde Staten, 83404
        • 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
      • Cedar Rapids, Iowa, Verenigde Staten, 52401
        • 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.
    • Kansas
      • Wichita, Kansas, Verenigde Staten, 67207
        • 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.
    • Maryland
      • Cumberland, Maryland, Verenigde Staten, 21502
        • 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.
      • Hagerstown, Maryland, Verenigde Staten, 21740
        • 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.
    • Massachusetts
      • Worcester, Massachusetts, Verenigde Staten, 01605
        • 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.
    • 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.
    • New York
      • Albany, New York, Verenigde Staten, 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.
      • Brooklyn, New York, Verenigde Staten, 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.
      • Mineola, New York, Verenigde Staten, 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.
    • North Carolina
      • Asheville, North Carolina, Verenigde Staten, 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.
      • Charlotte, North Carolina, Verenigde Staten, 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.
    • Ohio
      • Toledo, Ohio, Verenigde Staten, 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.
    • Oregon
      • Lake Oswego, Oregon, Verenigde Staten, 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.
      • Portland, Oregon, Verenigde Staten, 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.
    • South Carolina
      • Charleston, South Carolina, Verenigde Staten, 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.
      • Columbia, South Carolina, Verenigde Staten, 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.
      • North Charleston, South Carolina, Verenigde Staten, 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.
    • Tennessee
      • Hixon, Tennessee, Verenigde Staten, 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.
      • Jackson, Tennessee, Verenigde Staten, 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.
    • Texas
      • 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.
      • Houston, Texas, Verenigde Staten, 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.
    • Washington
      • Kennewick, Washington, Verenigde Staten, 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.
      • Seattle, Washington, Verenigde Staten, 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.

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:

  • Diagnose van matige tot ernstige AS met eerder gedocumenteerd radiologisch bewijs (röntgenfoto) dat voldoet aan de Modified New York-criteria voor AS (1984)
  • Heb actieve AS gedefinieerd als Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) ≥4 en de spinale pijn (rugpijn) score ≥4 op een numerieke beoordelingsschaal (NRS)
  • Deelnemers hadden niet-steroïde anti-inflammatoire geneesmiddelen (NSAID's) moeten gebruiken met een ontoereikende respons
  • Deelnemers die regelmatig NSAID's of cyclo-oxygenase-2 (COX-2)-remmers gebruiken als onderdeel van hun AS-therapie, moeten een stabiele dosis hebben
  • Deelnemers die een tumornecrosefactor-alfa (TNF)-remmer (niet meer dan één) hebben gebruikt, moeten een ontoereikende respons hebben ervaren
  • De totale duur van eerdere therapie (NSAID's en/of adequate fysiotherapie) moet ten minste 12 weken zijn
  • Mannen moeten ermee instemmen een betrouwbare anticonceptiemethode te gebruiken of zich tijdens het onderzoek te onthouden
  • Vrouwen moeten ermee instemmen om betrouwbare anticonceptie te gebruiken of zich te onthouden tijdens het onderzoek en gedurende ten minste 12 weken na het stoppen van de behandeling

Uitsluitingscriteria:

  • Deelnemers met een totale ankylose van de wervelkolom
  • Eerdere of huidige behandeling met adalimumab
  • Deelnemers die eerder zijn behandeld met biologische of andere immunomodulerende middelen, behalve degenen die gericht zijn op TNF
  • Bewijs van actieve inflammatoire artritische syndromen of andere spondyloartropathieën dan spondylitis ankylopoetica
  • Heeft deelgenomen aan een studie met interleukine-17 (IL-17)-antagonisten, waaronder ixekizumab
  • Ernstige aandoening of ziekte anders dan spondylitis ankylopoetica
  • Ernstige infectie in de afgelopen 3 maanden
  • Vrouwen die borstvoeding geven of borstvoeding geven (zogende vrouwen).

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
Experimenteel: Ixekizumab-doseringsschema 1
Toegediend door middel van 80 milligram (mg) subcutane (SC) injectie
SC toegediend
Andere namen:
  • LY2439821
Experimenteel: Ixekizumab-doseringsregime 2
Toegediend door 80 mg SC-injectie
SC toegediend
Andere namen:
  • LY2439821
Placebo-vergelijker: Placebo
Placebo voor ixekizumab en placebo voor adalimumab toegediend via SC-injectie
SC toegediend
Actieve vergelijker: Adalimumab
Toegediend door 40 mg SC-injectie
SC toegediend

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Werkzaamheid van Ixekizumab bij deelnemers met spondylitis ankylopoetica (AS). Maatregel: Beoordeling van spondyloartritis International Society Criteria (ASAS20)
Tijdsspanne: 16 weken
16 weken

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Werkzaamheid van Ixekizumab bij deelnemers met AS. Maatregel: ASAS
Tijdsspanne: 16 weken
16 weken
Kwaliteit van leven en resultaatbeoordelingen. Maatregelen: door de patiënt gerapporteerde resultaten (PRO)
Tijdsspanne: Basislijn tot en met 16 weken
Basislijn tot en met 16 weken
Werkzaamheid van Ixekizumab bij deelnemers met AS. Maatregel: Niet-artritische ziektebeoordelingen
Tijdsspanne: Basislijn tot en met 16 weken
Basislijn tot en met 16 weken
Werkzaamheid van Ixekizumab bij deelnemers met AS. Maatregel: perifere gewrichtstellingen
Tijdsspanne: 16 weken
16 weken
Werkzaamheid van Ixekizumab bij deelnemers met AS. Maatregel: spinale mobiliteit
Tijdsspanne: Basislijn tot en met 16 weken
Basislijn tot en met 16 weken
Werkzaamheid van Ixekizumab bij deelnemers met AS. Maatregel: gemodificeerde Stoke Ankylosing Spondylitis Spinal Score (mSASSS)
Tijdsspanne: Basislijn tot en met 108 weken
Basislijn tot en met 108 weken

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

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 juli 2014

Primaire voltooiing (Verwacht)

1 april 2016

Studie voltooiing (Verwacht)

1 april 2018

Studieregistratiedata

Eerst ingediend

3 juni 2013

Eerst ingediend dat voldeed aan de QC-criteria

3 juni 2013

Eerst geplaatst (Schatting)

6 juni 2013

Updates van studierecords

Laatste update geplaatst (Schatting)

16 september 2014

Laatste update ingediend die voldeed aan QC-criteria

15 september 2014

Laatst geverifieerd

1 september 2014

Meer informatie

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 .

Klinische onderzoeken op Spondylitis, ziekte van Bechterew

Klinische onderzoeken op Ixekizumab

3
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