671 Participants Needed

Duvakitug for Ulcerative Colitis

(SUNSCAPE-2 Trial)

Recruiting at 1 trial location
Age: Any Age
Sex: Any
Trial Phase: Phase 3
Sponsor: Sanofi
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment called duvakitug to determine its effectiveness for people with ulcerative colitis, a condition causing inflammation and sores in the colon. The study compares three different doses of duvakitug with a placebo (a treatment with no active drug) to identify the most effective dose. It aims to assess the long-term safety and effectiveness of duvakitug. Individuals with moderate to severe ulcerative colitis who have responded well to previous treatments might be suitable candidates for this trial. As a Phase 3 trial, it represents the final step before FDA approval, offering participants a chance to contribute to the potential availability of a new treatment.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the study team or your doctor.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that duvakitug is generally safe. In earlier studies, patients handled the treatment well, experiencing only a few side effects. Most participants reported mild to moderate reactions, common with new treatments, such as minor skin irritation at the injection site.

In another study on similar conditions, duvakitug showed promise in reducing inflammation, crucial for treating ulcerative colitis. This treatment is in the final stages of testing, indicating that its safety has been carefully evaluated so far. However, as with any treatment, some risk remains. Researchers will closely monitor participants to ensure their safety during the trial.12345

Why do researchers think this study treatment might be promising for Ulcerative Colitis?

Most treatments for ulcerative colitis, like mesalamine, corticosteroids, and biologics, focus on reducing inflammation in the colon. But Duvakitug works differently, targeting specific pathways involved in the immune response, which could mean more precise control of inflammation. Researchers are excited because Duvakitug is administered through a subcutaneous injection, which can be more convenient and less invasive compared to some other treatment methods like intravenous infusions. This combination of a new mechanism of action and a more patient-friendly delivery method makes Duvakitug a promising option for those with ulcerative colitis.

What evidence suggests that duvakitug might be an effective treatment for ulcerative colitis?

Research has shown that duvakitug may help treat ulcerative colitis. In one study, 36% of patients taking a 450 mg dose and 48% taking a 900 mg dose experienced significant symptom relief, compared to 20% who took a placebo (a pill with no active medicine). This indicates that many more people felt better with duvakitug than with no treatment. The treatment also led to improved results when doctors examined the intestines with a camera. This evidence suggests duvakitug could be very effective for people with moderate to severe ulcerative colitis.14678

Are You a Good Fit for This Trial?

This trial is for adults aged 18 to 80 with moderately to severely active Ulcerative Colitis. Eligible participants must have shown a clinical response in a previous study (SUNSCAPE-1) and completed an endoscopy. Those under 18 may join if they are fully physically developed.

Inclusion Criteria

I completed a specific previous study or its maintenance part.
I completed the SUNSCAPE-1 study and had a positive response.
I am between 18 and 80 years old, or 16-18 with full physical development.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Pivotal Maintenance Sub-Study

Participants receive the study medication or placebo for maintenance of ulcerative colitis

40 weeks
21 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

6 weeks
1 visit (in-person)

Open-Label Extension (OLE) Sub-Study

Participants may opt into continuation of treatment long-term with open-label duvakitug

240 weeks
11 visits (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • Duvakitug
Trial Overview The trial tests Duvakitug's long-term effectiveness and safety against a placebo in maintaining remission of Ulcerative Colitis symptoms over up to 286 weeks, including both a pivotal maintenance phase and an open-label extension where everyone gets the drug.
How Is the Trial Designed?
4Treatment groups
Experimental Treatment
Placebo Group
Group I: Duvakitug - dose 3Experimental Treatment1 Intervention
Group II: Duvakitug - dose 2Experimental Treatment1 Intervention
Group III: Duvakitug - dose 1Experimental Treatment1 Intervention
Group IV: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Sanofi

Lead Sponsor

Trials
2,246
Recruited
4,085,000+
Paul Hudson profile image

Paul Hudson

Sanofi

Chief Executive Officer since 2019

Degree in Economics from Manchester Metropolitan University

Christopher Corsico profile image

Christopher Corsico

Sanofi

Chief Medical Officer

MD from Cornell University, MPH in Chronic Disease Epidemiology from Yale University

Teva Branded Pharmaceutical Products R&D LLC

Industry Sponsor

Citations

Press Release: ECCO 2025: new duvakitug data reinforce ...ECCO 2025: new duvakitug data reinforce best-in-class potential in ulcerative colitis and Crohn's disease. New detailed data from the RELIEVE ...
OP41 Duvakitug (TEV-48574), an anti-TL1a monoclonal ...Both duvakitug doses successfully achieved the week 14 primary endpoint of clinical remission (36% [450 mg], 48% [900 mg] versus 20% [PBO]; PBO- ...
NCT07185009 | A Maintenance Study to Investigate the ...... Efficacy and Safety of Duvakitug in Participants With Moderately to Severely Active Ulcerative Colitis. Conditions. Ulcerative Colitis.
RELIEVE-UCCD: Duvakitug Improves Clinical, Endoscopic ...The RELIEVE-UCCD study showed duvakitug's efficacy in achieving clinical remission and endoscopic improvement in moderate to severe UC.
New data indicate duvakitug could “transform” IBD treatmentIn the CD cohort, 26% (450mg dose) and 48% (900mg dose) of patients treated with duvakitug achieved the primary endpoint of endoscopic response ...
NCT07184996 | An Induction Study to Investigate the ...This is a multinational, multicenter, randomized, double-blind, placebo-controlled, Phase 3 induction study to evaluate the efficacy and safety of duvakitug ...
Press Release: Duvakitug positive phase 2b results ...Duvakitug positive phase 2b results demonstrate best-in-class potential in ulcerative colitis and Crohn's disease. Primary endpoints met in ...
OP40 Duvakitug (TEV-48574), an anti-TL1a monoclonal ...Duvakitug has demonstrated reduced inflammation and fibrosis in colitis animal models.1 Few data are available for the potential of anti-TL1A ...
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