Tibulizumab Skin Healing and Inflammation Evaluation for Lasting Defense
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- Zura Bio Inc
- Study ID
- NCT06993610
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Hidradenitis Suppurativa (HS)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Tibulizumab Dose A — BIOLOGICALAnti BAFF/IL-17 antibody. ZB-106
- Tibulizumab Dose B — BIOLOGICALAnti BAFF/IL-17 antibody. ZB-106
- Placebo — OTHERZB-106 Placebo
Study Details
The study is a Phase 2, multi-center, randomized, double-blind, placebo-controlled study to evaluate the effects of tibulizumab over 16 weeks (Period 1) in adults with hidradenitis suppurativa, followed by a 16-week open-label extension period in which all participants will receive tibulizumab (Period 2)
Key Dates
- Start date
- May 16, 2025
- Status verified
- Feb 2026
- Primary completion
- Nov 30, 2026
- Completion
- Apr 30, 2027
Study Design
- Enrollment
- 225 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Tibulizumab Dose ASubcutaneous injection
- Experimental: Tibulizumab Dose BSubcutaneous injection
- Placebo Comparator: PlaceboSubcutaneous injection
Primary Outcome Measure
[Period 1] Percent change from baseline in abscess and inflammatory nodule (AN) count at 16 weeks [ Time Frame: Week 16 ]
Central Contacts
- Chief Medical Officer702-825-9872
Locations (31)
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