drugset / Trial / NCT03619902

A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Generalized Pustular Psoriasis

NCT03619902 ↗

Phase 2 Completed 8 enrolled Vanda Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The main objectives of this study are to evaluate the efficacy, safety and tolerability of imsidolimab in adults with active GPP.

Timeline

Start
2019-01-30
Primary completion
2021-01-20
Completion
2021-01-20

Outcome

Met primary endpoint

release “Six of 8 (75%) patients treated with imsidolimab monotherapy achieved the primary endpoint of improvement in the CGI scale on Day 29.” anaptysbio.com ↗

release “Imsidolimab demonstrated rapid and sustained efficacy with 6 of 8 (75%) generalized pustular psoriasis (GPP) patients achieving the primary endpoint” anaptysbio.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Imsidolimab Monoclonal antibody 100 mg Intravenous