A Study of JNJ-78934804 in Participants With Moderately to Severely Active Crohn's Disease (DUET ENCORE-CD)
27. august 2026 opdateret af: Janssen Research & Development, LLC
A Phase 3, Randomized, Double-blind, and Active-controlled Multicenter Study to Evaluate the Efficacy and Safety of JNJ-78934804 in Participants With Moderately to Severely Active Crohn's Disease
The purpose of this study is to assess how well JNJ-78934804 works (efficacy) and how safe it is (safety) as compared to guselkumab at Week 48 in participants with moderately to severely active Crohn's disease (a long-term, progressive [worsens with time] and life-threatening disease of the intestine).
Studieoversigt
Status
Rekruttering
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
460
Fase
- Fase 3
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Study Contact
- Telefonnummer: 844-434-4210
- E-mail: Participate-In-This-Study1@its.jnj.com
Studiesteder
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AAI, Argentina, C1425BGC
- Rekruttering
- GEDYT
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La Plata, Argentina, 1896
- Rekruttering
- Globalpsy
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Mendoza, Argentina, M5500DPS
- Rekruttering
- HIGEA
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Quilmes, Argentina, B1878DVB
- Rekruttering
- Cer Instituto Medico
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Adelaide, Australien, 5000
- Rekruttering
- Banksia Trials SA
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Camperdown, Australien, 2050
- Rekruttering
- Royal Prince Alfred Hospital
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Clayton, Australien, 3168
- Rekruttering
- Monash Medical Centre
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East Melbourne, Australien, 3002
- Rekruttering
- The Melbourne Gut Clinic Epworth Hospital
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Kurralta Park, Australien, 5037
- Rekruttering
- IBD SA
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New Lambton Heights, Australien, 2305
- Rekruttering
- John Hunter Hospital
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South Brisbane, Australien, 4101
- Rekruttering
- Mater Misericordiae Hospital
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Edegem, Belgien, 2650
- Rekruttering
- Universitair Ziekenhuis Antwerpen
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Ghent, Belgien, 9000
- Rekruttering
- Ghent University Hospital
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Leuven, Belgien, 3000
- Rekruttering
- Universitair Ziekenhuis Leuven
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Roeselare, Belgien, 8800
- Rekruttering
- Algemeen Ziekenhuis Delta
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Curitiba, Brasilien, 80430 180
- Rekruttering
- CDC - Centro Digestivo de Curitiba
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Macaé, Brasilien, 27910-020
- Rekruttering
- Cliged
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Porto Alegre, Brasilien, 90035 903
- Rekruttering
- Hospital de Clinicas de Porto Alegre
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Porto Alegre, Brasilien, 90160 093
- Rekruttering
- Hospital Ernesto Dornelles
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Santo André, Brasilien, 09080-110
- Rekruttering
- Pesquisare Saúde
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São Paulo, Brasilien, 01236 030
- Rekruttering
- BR Trials
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São Paulo, Brasilien, 04077-020
- Rekruttering
- Rocco And Nazato Servicos Medicos Ltda
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Votuporanga, Brasilien, 15500-269
- Rekruttering
- Integral Pesquisa e Ensino
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Alberta
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Edmonton, Alberta, Canada, T5R 1W2
- Rekruttering
- Gastroenterology and Internal Medicine Research Institute (GIRI)
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Edmonton, Alberta, Canada, Code: T6K 4B2
- Rekruttering
- South Edmonton Gastroenterology Research Clinic
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British Columbia
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Vancouver, British Columbia, Canada, V6Z 2K5
- Rekruttering
- GI Research Institute (G.I.R.I.)
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Nova Scotia
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Kentville, Nova Scotia, Canada, B4N 0A3
- Rekruttering
- Viable Clinical Research
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Ontario
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London, Ontario, Canada, N6K 1M6
- Rekruttering
- London Digestive Disease Institute
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Mississauga, Ontario, Canada, L5M 2S4
- Rekruttering
- West GTA Research Inc
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Toronto, Ontario, Canada, M6A 3B4
- Rekruttering
- Toronto Immune and Digestive Health Institute Inc
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Quebec
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Montreal, Quebec, Canada, H2X 0C1
- Rekruttering
- CHUM - Centre hospitalier universitaire de Montreal
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Montreal, Quebec, Canada, H3H1E3
- Rekruttering
- Clinique IMD
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California
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Anaheim, California, Forenede Stater, 92805
- Rekruttering
- Clinnova Research
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Chula Vista, California, Forenede Stater, 91910
- Rekruttering
- Gastro SB Clinic
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Los Alamitos, California, Forenede Stater, 90720
- Rekruttering
- United Medical Doctors
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San Diego, California, Forenede Stater, 92123
- Rekruttering
- Medical Associates Research Group, Inc.
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Colorado
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Colorado Springs, Colorado, Forenede Stater, 80907
- Rekruttering
- Peak Gastroenterology Associates
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Florida
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Lakewood Rch, Florida, Forenede Stater, 34211
- Rekruttering
- Florida Research Center Inc.
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Miami, Florida, Forenede Stater, 33157-6575
- Rekruttering
- Sanchez Clinical Research, Inc
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Tampa, Florida, Forenede Stater, 33609
- Rekruttering
- GCP Clinical Research
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Georgia
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Suwanee, Georgia, Forenede Stater, 30024
- Rekruttering
- Atlanta Gastroenterology Specialists
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Kentucky
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Crestview Hills, Kentucky, Forenede Stater, 41017
- Rekruttering
- Tri-State Gastroenterology Assoc
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Louisiana
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Lafayette, Louisiana, Forenede Stater, 70503
- Rekruttering
- Gastroenterology Clinic of Acadiana
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Michigan
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Farmington Hills, Michigan, Forenede Stater, 48334
- Rekruttering
- Michigan Center of Medical Research
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New York
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New York, New York, Forenede Stater, 10075
- Rekruttering
- New York Gastroenterology Associates
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North Carolina
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Chapel Hill, North Carolina, Forenede Stater, 27599
- Rekruttering
- University of North Carolina Hospital
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Ohio
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Mentor, Ohio, Forenede Stater, 44060
- Rekruttering
- Great Lakes Gastroenterology Research, LLC
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Oklahoma
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Oklahoma City, Oklahoma, Forenede Stater, 73114
- Rekruttering
- Digestive Disease Specialists Inc
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Oregon
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Portland, Oregon, Forenede Stater, 97220
- Rekruttering
- The Oregon Clinic
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Tennessee
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Cordova, Tennessee, Forenede Stater, 38018
- Rekruttering
- Gastro One
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Texas
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Tyler, Texas, Forenede Stater, 75701
- Rekruttering
- Tyler Research Institute, LLC
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Washington
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Tacoma, Washington, Forenede Stater, 98405
- Rekruttering
- GI Alliance Tacoma
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Nantes, Frankrig, 44000
- Rekruttering
- CHU de Nantes hotel Dieu
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Reims, Frankrig, 51100
- Rekruttering
- CHU de Reims
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Nijmegen, Holland, 6525 GA
- Rekruttering
- Radboud Umcn
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Hubballi, Indien, 580021
- Rekruttering
- Sushruta Multispecialty Hospital and Research Centre
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Hyderabad, Indien, 500032
- Rekruttering
- Asian Institute of Gastroenterology
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Jaipur, Indien, 302006
- Rekruttering
- S. R. Kalla Memorial General Hospital
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Kochi, Indien, 682018
- Rekruttering
- Lisie Hospital
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Secunderabad, Indien, 500003
- Rekruttering
- Yashoda Super Speciality Hospitals
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Surat, Indien, 395002
- Rekruttering
- SIDS (Surat Institute of Digestive Sciences) Hospital and Research Centre
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Surat, Indien, 395009
- Rekruttering
- Gujarat Gastro and Vascular Hospital
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Ashdod, Israel, 7747629
- Rekruttering
- Assuta Medical Center
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Haifa, Israel, 3109601
- Rekruttering
- Rambam Medical Center
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Haifa, Israel, 31048
- Rekruttering
- Bnai Zion Medical Center
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Holon, Israel, 5822012
- Rekruttering
- Wolfson Medical Center
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Jerusalem, Israel, 9103102
- Rekruttering
- Shaare Zedek Medical Center
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Kfar Saba, Israel, 44281
- Rekruttering
- Meir Medical Center
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Nahariya, Israel, 2210001
- Rekruttering
- Galilee Medical Center
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Petah Tikva, Israel, 4941492
- Rekruttering
- Rabin Medical Center
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Ramat Gan, Israel, 52621
- Rekruttering
- Sheba medical center
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Tel Aviv, Israel, 64239
- Rekruttering
- Tel Aviv Sourasky Medical Center
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Hamamatsu, Japan, 431-3192
- Rekruttering
- Hamamatsu University Hospital
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Hirosaki, Japan, 036-8545
- Rekruttering
- National Hospital Organization Hirosaki National Hospital
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Kagoshima, Japan, 892-0843
- Rekruttering
- Kagoshima IBD Gastroenterology Clinic
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Kashiwa, Japan, 277-0871
- Rekruttering
- Tsujinaka Hospital Kashiwanoha
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Kobe, Japan, 650 0017
- Rekruttering
- Kobe University Hospital
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Kumamoto, Japan, 860-8556
- Rekruttering
- Kumamoto University Hospital
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Kumamoto, Japan, 861-8520
- Rekruttering
- Japanese Red Cross Kumamoto Hospital
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Kumamoto, Japan, 862-0971
- Rekruttering
- Takano Hospital
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Minatoku, Japan, 108-8642
- Rekruttering
- Kitasato University Kitasato Institute Hospital
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Nagoya, Japan, 467-8602
- Rekruttering
- Nagoya City University Hospital
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Osaka, Japan, 540-0006
- Rekruttering
- National Hospital Organization Osaka National Hospital
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Osaka, Japan, 543-8555
- Rekruttering
- Japanese Red Cross Osaka Hospital
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Sapporo, Japan, 065-0033
- Rekruttering
- Sapporo Higashi Tokushukai Hospital
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Sapporo, Japan, 060-0033
- Rekruttering
- Hokkaido P.W.F.A.C. Sapporo-Kosei General Hospital
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Shimizu, Japan, 411-8611
- Rekruttering
- National Hospital Organization Shizuoka Medical Center
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Takamatsu, Japan, 760-0017
- Rekruttering
- Takamatsu Red Cross Hospital
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Yamanashi, Japan, 400-8506
- Rekruttering
- Yamanashi Prefectural Central Hospital
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Beijing, Kina, 100191
- Rekruttering
- Peking University Third Hospital
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Changzhou, Kina, 213004
- Rekruttering
- Changzhou No 2 Peoples Hospital
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Chongqing, Kina, 400014
- Rekruttering
- Chongqing General Hospital
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Guangzhou, Kina, 510655
- Rekruttering
- Sun Yat-sen University - The Sixth Affiliated Hospital Guangdong Gastrointestinal Hospital
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Hangzhou, Kina, 310000
- Rekruttering
- Sir Run Run Shaw Hospital Zhejiang University School of Medicine
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Huai'an, Kina, 223300
- Rekruttering
- Huai'an 1st Hospital
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Ningbo, Kina, 315041
- Rekruttering
- Ningbo Medical Center Lihuili Hospital
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Zhuzhou, Kina, 412007
- Rekruttering
- Zhuzhou Central Hospital
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Ampang, Malaysia, 68000
- Rekruttering
- Hospital Ampang
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Kajang, Malaysia, 43000
- Rekruttering
- Sultan Idris Shah Hospital
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Kota Kinabalu, Malaysia, 88586
- Rekruttering
- Hospital Queen Elizabeth
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Kuala, Malaysia, 20400
- Rekruttering
- Hospital Sultanah Nur Zahirah
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Petaling Jaya, Malaysia, 50603
- Rekruttering
- University Malaya Medical Centre
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Tromsø, Norge, 9038
- Rekruttering
- Universitetssykehuset Nord-Norge HF
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Trondheim, Norge, 7030
- Rekruttering
- St. Olavs Hospital
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Ålesund, Norge, 6017
- Rekruttering
- Alesund sjukehus
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Bydgoszcz, Polen, 85 229
- Rekruttering
- Centrum Medyczne Medis ManerMed Sp Z O O
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Krakow, Polen, 31-513
- Rekruttering
- Centrum Medyczne PROMED
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Lublin, Polen, 20 582
- Rekruttering
- Medrise Sp. z o.o.
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Rzeszów, Polen, 35-055
- Rekruttering
- Centrum Medyczne 'Medyk' Sp. z o.o. K.
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Szczecin, Polen, 71-434
- Rekruttering
- Twoja Przychodnia - Szczecinskie Centrum Medyczne
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Zamość, Polen, 22 400
- Rekruttering
- ETG Zamość
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Braga, Portugal, 4710 243
- Rekruttering
- Uls Braga - Hosp. Braga
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Viana do Castelo, Portugal, 4900-408
- Rekruttering
- Ulsam - Hosp. Santa Luzia
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Banská Bystrica, Slovakiet, 975 17
- Rekruttering
- FNsP F. D. Roosevelta Banska Bystrica
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Bratislava, Slovakiet, 811 09
- Rekruttering
- Cliniq s.r.o.
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Košice, Slovakiet, 040 13
- Rekruttering
- ENDOMED s.r.o
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Nitra, Slovakiet, 949 01
- Rekruttering
- KM Management spol. s r.o.
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Prešov, Slovakiet, 080 01
- Rekruttering
- GASTRO I. s.r.o.
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Prešov, Slovakiet, 080 01
- Rekruttering
- Gastro LM s.r.o.
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Madrid, Spanien, 28031
- Rekruttering
- Hosp. Univ. Infanta Leonor
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Vigo, Spanien, 36312
- Rekruttering
- Hosp. Alvaro Cunqueiro
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Busan, Sydkorea, 48108
- Rekruttering
- Inje University Haeundae Paik Hospital
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Daejeon, Sydkorea, 34943
- Rekruttering
- The Catholic University of Korea Daejeon St Mary's Hospital
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Gangnam Gu, Sydkorea, 06351
- Rekruttering
- Samsung Medical Center
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Seoul, Sydkorea, 05505
- Rekruttering
- Asan Medical Center
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Taoyuan, Taiwan, 333
- Rekruttering
- Linkou Chang Gung Memorial Hospital
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Hradec Králové, Tjekkiet, 500 12
- Rekruttering
- Hepato-gastroenterologie HK, s.r.o.
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Prague, Tjekkiet, 190 00
- Rekruttering
- ISCARE a.s.
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Prague, Tjekkiet, 14000
- Rekruttering
- Fakultni Thomayerova nemocnice
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Antalya, Tyrkiet (Türkiye), 07100
- Rekruttering
- Antalya Training and Research Hospital
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Istanbul, Tyrkiet (Türkiye), 34899
- Rekruttering
- Marmara University Pendik Training Hospital
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Istanbul, Tyrkiet (Türkiye), 34093
- Rekruttering
- Bezmialem University Medical Faculty
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Izmir, Tyrkiet (Türkiye), 35540
- Rekruttering
- Izmir Şehir Hastanesi
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Kocaeli, Tyrkiet (Türkiye), 41001
- Rekruttering
- Kocaeli University Medical Faculty
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Mersin, Tyrkiet (Türkiye), 33343
- Rekruttering
- Mersin University Medical Faculty
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Berlin, Tyskland, 14163
- Rekruttering
- Krankenhaus Waldfriede Mitte
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Dresden, Tyskland, 01307
- Rekruttering
- Universitätsklinikum Carl Gustav Carus Dresden
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Hanover, Tyskland, 30625
- Rekruttering
- Medizinische Hochschule Hannover
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Kiel, Tyskland, 24105
- Rekruttering
- Universitatsklinikum Schleswig Holstein Kiel
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Leipzig, Tyskland, 04103
- Rekruttering
- EUGASTRO GmbH
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Mannheim, Tyskland, 68167
- Rekruttering
- Universitaetsklinikum Mannheim
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Rostock, Tyskland, 18057
- Rekruttering
- Universitaetsmedizin Rostock
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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
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion criteria:
- Have a diagnosis of Crohn's disease (CD) or fistulizing CD established greater than or equal to (>=) 12 weeks before screening including both endoscopic evidence and a histopathology report consistent with a diagnosis of CD
- Have moderately to severely active CD based on crohn's disease activity index (CDAI) criteria defined as a baseline CDAI score >= 220 but less than or equal to (<=) 450 and either: a. Mean daily stool frequency (SF) count >= 4.0, based on the unweighted CDAI component of the number of liquid or very soft stools or b. Mean daily AP score >= 2.0, based on the unweighted CDAI component of abdominal pain (AP)
- Have moderately to severely active ileal and/or colonic CD as assessed by central review of the screening video ileocolonoscopy based on simple endoscopic score for crohn's disease (SES-CD) criteria
- Have had an inadequate initial response, loss of response, or intolerance to previously approved systemic therapies
Exclusion criteria:
- Diagnosis of indeterminate colitis, microscopic colitis, ischemic colitis, ulcerative colitis (UC) or clinical findings highly suggestive of UC
- Complications of CD such as symptomatic bowel strictures or stenoses, or any other manifestation that may require intestinal surgery while enrolled in the study
- Presence of draining (that is, functioning) stoma or ostomy
- Has a history of short bowel syndrome, is missing greater than (>) 2 of the 5 ileocolonic segments, or has any other medical condition that could preclude or confound the ability to use efficacy assessment tools (such as CDAI) to assess response to study intervention
- Currently has or is suspected of having an abscess
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: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: JNJ-78934804
Participants will receive JNJ-78934804 induction dose, at Weeks 0, 4, and 8 followed by JNJ-78934804 maintenance dose, once every 4 weeks (q4w) starting at Week 12.
All participants who meet the rescue criteria will receive JNJ-78934804 induction dose at Weeks 16, 20, and 24 followed by JNJ-78934804 maintenance dose q4w starting at Week 28.
Participants who complete double-blind treatment phase (Week 48) and who may benefit from continued study intervention in the opinion of the investigator will have the opportunity to enter the long-term extension (LTE) phase.
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JNJ-78934804 will be administered subcutaneously.
Andre navne:
|
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Aktiv komparator: Guselkumab
Participants will receive guselkumab induction dose at Weeks 0, 4, and 8 followed by guselkumab maintenance dose q4w starting at Week 12.
All participants who meet the rescue criteria will receive JNJ-78934804 induction dose at Weeks 16, 20, and 24 followed by JNJ-78934804 maintenance dose q4w starting at Week 28.
Participants who complete double-blind treatment phase (Week 48) and who may benefit from continued study intervention in the opinion of the investigator will have the opportunity to enter the LTE phase.
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Guselkumab vil blive administreret subkutant.
Andre navne:
JNJ-78934804 will be administered subcutaneously.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Co-Primary: Percentage of Participants with Clinical Remission at Week 48
Tidsramme: At Week 48
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Clinical remission is defined as a Crohn's Disease Activity Index (CDAI) score less than (<) 150.
CDAI scores range from 0 to approximately 600.
Higher score indicates higher disease activity.
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At Week 48
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Co-Primary: Percentage of Participants with Endoscopic Remission at Week 48
Tidsramme: At Week 48
|
Endoscopic remission is defined as a Simple Endoscopic Score for Crohn's Disease (SES-CD) score of less than or equal to (<=) 4 with at least a 2-point reduction from baseline and no subscore greater than (>) 1 in any individual component.
The SES-CD is based on the evaluation of 4 endoscopic components (presence/size of ulcers, proportion of mucosal surface covered by ulcers, proportion of mucosal surface affected by any lesions, and presence/type of narrowing/strictures) across 5 ileocolonic segments.
SES-CD score can range from 0 to 56.
Higher scores indicating more severe disease.
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At Week 48
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Percentage of Participants with Deep Remission at Week 48
Tidsramme: At Week 48
|
Deep remission (composite endpoint) is defined as achieving both clinical remission and endoscopic remission at Week 48 at the participant level.
Clinical remission is defined as a CDAI score of <150 and Endoscopic remission is defined as a SES-CD score of <= 4 with at least a 2-point reduction from baseline and no subscore >1 in any individual component.
CDAI scores range from 0 to approximately 600.
Higher score indicates higher disease activity.
SES-CD score can range from 0 to 56.
Higher scores indicating more severe disease.
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At Week 48
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Percentage of Participants with Corticosteroid-Free (90-Day) Clinical Remission at Week 48
Tidsramme: At Week 48
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Corticosteroid-free (90-day) clinical remission at Week 48 is defined as clinical remission at Week 48 and not receiving corticosteroids for at least 90 days prior to Week 48.
Clinical remission is defined as a CDAI score of <150.
CDAI scores range from 0 to approximately 600.
Higher score indicates higher disease activity.
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At Week 48
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Percentage of Participants with Corticosteroid-Free (90-day) PRO-2 Remission at Week 48
Tidsramme: At Week 48
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Corticosteroid-free (90-day) patient-reported outcome(s) (PRO-2) remission at Week 48 is defined as an abdominal plan (AP) mean daily score less than or equal to (<=) 1 and stool frequency (SF) mean daily score <= 2.8, and no worsening of AP or SF from baseline, and not receiving corticosteroids for at least 90 days prior to Week 48.
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At Week 48
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Percentage of Participants with Sustained Clinical Remission
Tidsramme: At Weeks 12 and 48
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Sustained clinical remission is defined as clinical remission at Week 12 and Week 48.
Clinical remission is defined as CDAI score of <150.
CDAI scores range from 0 to approximately 600.
Higher score indicates higher disease activity.
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At Weeks 12 and 48
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Percentage of Participants with Histologic-Endoscopic Remission at Week 48
Tidsramme: At Week 48
|
Histologic-endoscopic remission at week 48 is defined as achieving a combination of histologic remission and endoscopic remission at Week 48.
Histologic remission is defined as absence of neutrophils from the mucosa (both lamina propria and epithelium), no crypt destruction, and no erosions, or ulcerations or granulation tissue as assessed by the Robarts Histopathology Index.
Endoscopic remission is defined as a SES-CD score of <= 4 with at least a 2-point reduction from baseline and no subscore > 1 in any individual component.
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At Week 48
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Percentage of Participants with Inflammatory Bowel Disease Questionnaire (IBDQ) Response at Week 48
Tidsramme: At Week 48
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IBDQ response at Week 48 is defined as an improvement of at least 16 points in the IBDQ total score from baseline at Week 48.
IBDQ is a validated, 32-item, self-reported questionnaire for participants with IBD that will be used to evaluate disease-specific health related quality of life (HRQoL) across 4 dimensional scores: bowel symptoms (loose stools, AP), systemic function (fatigue, altered sleep pattern), social function (work attendance, need to cancel social events), and emotional function (anger, depression, irritability).
Scores range from 32 to 224, with higher scores indicating better outcomes.
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At Week 48
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Percentage of Participants with Patient-Reported Outcomes Measurement Information System 29 (PROMIS-29) Mental Component Summary Score (MCS) Response at Week 48
Tidsramme: At Week 48
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PROMIS-29 MCS response at Week 48 is defined as an improvement of at least 7 points in PROMIS-29 MCS score from baseline at Week 48.
The PROMIS-29 is a collection of short forms containing 4 items for each of 7 domains (depression, anxiety, physical function, pain interference, fatigue, sleep disturbance, and ability to participate in social roles and activities).
PROMIS-29 also includes an overall average pain intensity 0-10 numeric rating scale.
The PROMIS-29 MCS will be assessed, which is primarily informed by domains of emotional distress (depression/anxiety) and fatigue as well as sleep disturbance where higher MCS scores reflect better mental health.
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At Week 48
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Percentage of Participants with Clinical Remission at Week 12
Tidsramme: At Week 12
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Clinical remission at Week 12 is defined as CDAI score <150 at Week 12. CDAI scores range from 0 to approximately 600.
Higher score indicates higher disease activity.
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At Week 12
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Percentage of Participants with Endoscopic Response at Week 12
Tidsramme: At Week 12
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Endoscopic response at Week 12 is defined as greater than (>) 50 percent (%) improvement from baseline in SES-CD score at Week 12 or a decrease of at least 2 points in participants with a baseline score of 4 and isolated ileal disease.
SES-CD score can range from 0 to 56.
Higher scores indicating more severe disease.
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At Week 12
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Number of Participants with Adverse Events (AE) and Serious AEs (SAEs)
Tidsramme: Up to approximately 3 years
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An AE is any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non investigational) product.
An AE does not necessarily have a causal relationship with the intervention.
An SAE is any untoward medical occurrence that at any dose: results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, is a suspected transmission of any infectious agent via a medicinal product, and is medically important.
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Up to approximately 3 years
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Studieleder: Janssen Research & Development, LLC Clinical Trial, Janssen Research & Development, LLC
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 (Faktiske)
22. maj 2026
Primær færdiggørelse (Anslået)
12. juni 2028
Studieafslutning (Anslået)
12. juli 2030
Datoer for studieregistrering
Først indsendt
5. maj 2026
Først indsendt, der opfyldte QC-kriterier
5. maj 2026
Først opslået (Faktiske)
11. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
28. august 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
27. august 2026
Sidst verificeret
1. august 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 78934804CRD3001
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
JA
IPD-planbeskrivelse
The data sharing policy of Johnson & Johnson Innovative Medicine is available at www.innovativemedicine.jnj.com/our-innovation/clinical-trials/transparency.
As noted on this site, requests for access to the study data can be submitted through Yale Open Data Access (YODA) Project site at yoda.yale.edu.
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ja
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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 .