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Taking people in United StatesPhase 3

Tests duvakitug to maintain remission in ulcerative colitis

Tests duvakitug against placebo in adults with active ulcerative colitis.

Plain-language title generated from the registry record
Registry title: A Maintenance Study to Investigate the Efficacy and Safety of Duvakitug in Participants With Moderately to Severely Active Ulcerative Colitis

Key facts

Where
Atlanta, Baton Rouge, Chesterfield, Colorado Springs, Columbus, Coronado, Fayetteville, Gurnee, Idaho Falls, Kingwood, Kissimmee, Lexington, Liberty, Lubbock, Mandeville, Maspeth, Miami, Monroe, Murrieta, New Albany, New York, Pittsburgh, Providence, San Antonio, Southlake, Sparta, Tampa, Tucson, Tyler, Vancouver, Victorville, Westlake, Worcester, and Wyoming, United StatesSee the 37 sites
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 16 and 80 years old?

Source: NCT07185009, who can take part

Where in United States

  • Atlanta Gastroenterology Associates-Site Number: 8400109Atlanta, United StatesTaking people
  • GI Alliance - Baton Rouge-Site Number: 8400129Baton Rouge, United StatesTaking people
  • ChesterfieldChesterfield, United StatesTaking people
  • Peak Gastroenterology Associates - Colorado Springs-Site Number: 8400039Colorado Springs, United StatesTaking people
  • Ohio Gastroenterology Group Inc.-Site Number: 8400006Columbus, United StatesTaking people
  • Southern California GI & Liver Centers-Site Number: 8400062Coronado, United StatesTaking people
  • Cross Creek Medical Clinic-Site Number: 8400057Fayetteville, United StatesTaking people
  • GI Alliance - Gurnee-Site Number:Gurnee, United StatesTaking people
  • Grand Teton Research Group, PLLC-Site Number: 8400127Idaho Falls, United StatesTaking people
  • One of a Kind Clinical Research Center TX, LLC-Site Number; 8400125Kingwood, United StatesTaking people
  • Clinical Research of Osceola-Site Number: 8400013Kissimmee, United StatesTaking people
  • University of Kentucky Hospital/UK Albert B. Chandler Hospital-Site Number: 8400058Lexington, United StatesTaking people
  • BVL Clinical Research-Site Number: 8400005Liberty, United StatesTaking people
  • GI Alliance - Lubbock-Site Number: 8400092Lubbock, United StatesTaking people
  • Texas Digestive Disease Consultants, PLLC d/b/a GI Alliance - Mandeville-Site Number: 8400128Mandeville, United StatesTaking people
  • MedTraits NY-Site Number: 8400045Maspeth, United StatesTaking people
  • Bioresearch Partner-Kendale Lakes-Site Number: 8400053Miami, United StatesTaking people
  • Delta Research Partners-Site Number: 8400087Monroe, United StatesTaking people
  • United Medical Doctors CA-Site Number: 8400044Murrieta, United StatesTaking people
  • Gastroenterology Health Partners, PLLC - New Albany-Site Number: 8400100New Albany, United StatesTaking people
  • Lenox Hill Hospital-Site Number: 8400052New York, United StatesTaking people
  • New York Gastroenterology Associates-Site Number: 8400009New York, United StatesTaking people
  • NYU Langone Health-Site Number: 8400091New York, United StatesTaking people
  • Weill Cornell Medicine - NewYork-Presbyterian Hospital-Site Number: 8400040New York, United StatesTaking people
  • The Allegheny Health Network (AHN) Center for Digestive Health-Site Number: 8400107Pittsburgh, United StatesTaking people
  • University Gastroenterology-Site Number: 8400103Providence, United StatesTaking people
  • Gastroenterology Research of San Antonio LLC-Site Number: 8400054San Antonio, United StatesTaking people
  • Texas Digestive Disease Consultants, PLLC. dba GI Alliance - Southlake - Corporate Office-Site Number: 8400101Southlake, United StatesTaking people
  • Premier Health Research, LLC-Site Number: 8400114Sparta, United StatesTaking people
  • NMC Research LLC-Site Number: 8400033Tampa, United StatesTaking people
  • Del Sol Research Management, LLC-Site Number: 8400012Tucson, United StatesTaking people
  • Tyler Research Institute, LLC-Site Number: 8400095Tyler, United StatesTaking people
  • The Vancouver Clinic Inc. P.S.-Site Number: 8400090Vancouver, United StatesTaking people
  • Om Research, LLC - Victorville-Site Number: 8400022Victorville, United StatesTaking people
  • North Shore Gastroenterology Research-Site Number: 8400130Westlake, United StatesTaking people
  • UMass Memorial Medical Center-Site Number: 8400121Worcester, United StatesTaking people
  • Gastroenterology Associates of Western Michigan-Site Number: 8400060Wyoming, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Sanofi
Trial code
NCT07185009
Record updated
16 October 2026
Original description
This is a multicenter, randomized, double-blind, placebo-controlled Phase 3 maintenance study to evaluate the efficacy and safety of duvakitug in participants with moderately to severely active Ulcerative Colitis (UC).Read full original descriptionShow less

A Multicenter, Multinational, Randomized, Double-blind, Placebo-Controlled, Phase 3 Maintenance Study to Evaluate the Efficacy and Safety of Duvakitug in Participants With Moderately to Severely Active Ulcerative Colitis

This is a multicenter, randomized, double-blind, placebo-controlled Phase 3 maintenance study to evaluate the efficacy and safety of duvakitug in participants with moderately to severely active Ulcerative Colitis (UC).

Study details include:

The study duration may be up to 286 weeks including:

* 40-week Pivotal Maintenance Sub-Study * 240-week Open-Label Extension (OLE) Sub-Study * 45-day Follow-up Visit Note: For the participants who do not enroll into OLE Sub-Study, the duration will be up to 46 weeks, including the 40-week maintenance period and a 45-day follow-up visit.

The treatment duration may be up to 280 weeks including:

* 40 weeks in Pivotal Maintenance Sub-Study * 240 weeks in OLE Sub-Study

The total number of on-site visit will be up to 32:

* 21 visits in the Pivotal Maintenance Sub-Study. * 11 visits in the OLE Sub-Study.

Inclusion: Participants aged ≥18 and ≤80 years of age at Baseline. (Where locally permissible, participants 16 to <18 years of age who meet the definition of Tanner stage 5 for development); Pivotal Maintenance Sub-Study: Participants who achieved clinical response and completed endoscopy at the end of SUNSCAPE-1; OLE Sub-Study: Participants who complete the Pivotal Maintenance Sub-Study or participation in the TV48574-IMM-20038 Study.

Exclusion: Participants with medical or compliance conditions that are deemed unsuitable for the study by the investigator; Participants with a known hypersensitivity to duvakitug that makes the participant unsuitable for the study by the investigator; The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

ClinicalTrials.gov NCT07185009