Overview
A Phase 2b Study to Evaluate RIST4721 in Palmoplantar Pustulosis (PPP)
Status:
Recruiting
Recruiting
Trial end date:
2023-05-30
2023-05-30
Target enrollment:
0
0
Participant gender:
All
All
Summary
A Randomized, Double-blind, Placebo-controlled, Dose Ranging Phase 2 Study to Evaluate the Efficacy and Safety of RIST4721 in Subjects with Palmoplantar PustulosisPhase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Aristea Therapeutics, Inc.
Criteria
Inclusion Criteria:- At least 6 months history of moderate or severe PPP, as defined by PPPASI ≥12 and
PPPGA ≥3 at screening
- Males and females must be willing to use birth control as indicated
Exclusion Criteria:
- Moderate to severe psoriasis covering ≥10% of total body surface area (BSA) at
screening
- Breastfeeding or pregnant
- Known immunodeficiency or subject is immunocompromised
- Active/latent infection with HBV, HCV, HIV, SARS-CoV-2 or TB
- Any topical medications for PPP excluding emollients within two weeks of randomization
and systemic therapies (including phototherapy) within 4 weeks of randomization