Combination CurQD and Vedolizumab in Ulcerative Colitis
Part of paid clinical trials in New York, New York.
- Sponsor
- Ryan C Ungaro
- Study ID
- NCT07665294
- Phase
- PHASE4
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- CurQD — DRUGCapsule doses 235mg - 385mg curcumin/150mg-300mg QingDai
- Placebo — DRUGMatching capsules
- Vedolizumab — DRUGas prescribed by participant's provider as part of routine clinical care
Study Details
The purpose of this research study is to test the efficacy and safety of the study intervention, CurQD or placebo (non-active pill), in combination with vedolizumab prescribed as standard of care for patients with ulcerative colitis (UC)..
Key Dates
- Start date
- Jun 24, 2026
- Status verified
- Jun 2026
- Primary completion
- Jun 23, 2027
- Completion
- Jun 23, 2027
Study Design
- Enrollment
- 160 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: CurQDCurQD in 1-2 oral capsules twice a day, increasing doses up to 30 weeks. Dose ranging from 470-1540mg curcumin and 300mg-600mg QingDai
- Placebo Comparator: PlaceboPlacebo comparator in same dosing frequency
Primary Outcome Measure
Number of participants with clinical remission [ Time Frame: Week 14 ]
Central Contacts
- Nicole Lewis212-468-2174
- Miriam San Lucas
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Icahn School of Medicine at Mount Sinai | New York | New York | 10029 | - |
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