Overview

A Phase 2b Study to Evaluate RIST4721 in Palmoplantar Pustulosis (PPP)

Status:
Recruiting
Trial end date:
2023-05-30
Target enrollment:
0
Participant gender:
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 Pustulosis
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
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