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Clinical Trial Summary

Proof of concept study to assess the safety and tolerability of AX-158 in patients with mild to moderate psoriasis. Patients will be evaluated for a 28-day treatment period with either AX-158 or Placebo and then followed for an additional 30 days for safety.


Clinical Trial Description

This is a Phase 2a Proof of Concept randomized, double-blind, placebo-controlled study to investigate the safety and tolerability of AX-158 in patients with mild to moderate Psoriasis. Participants will be randomized 2:1 to receive AX-158 or Placebo. A total of 30 participants will be treated for 28 days and followed for an additional 30 days for safety. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05725057
Study type Interventional
Source Artax Biopharma Inc
Contact Suzanne Crowley, MS, BSN
Phone 321-266-9347
Email ax-158-1011@artaxbiopharma.com
Status Recruiting
Phase Phase 1/Phase 2
Start date November 30, 2023
Completion date December 2024

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