CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 45 enrolled
Drug / intervention
750 mg Imsidolimab +2 moredrug
Likely dose
750 mg Imsidolimabfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05352893
NCT05352893Phase 3Completed

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Adult Subjects With Generalized Pustular Psoriasis

Vanda Pharmaceuticals·interventional·Posted Apr 29, 2022·Updated Mar 17, 2026

In Brief

A Phase 3 clinical trial evaluating 750 mg Imsidolimab, 300 mg Imsidolimab, and 1 other intervention for Generalized Pustular Psoriasis. Completed, enrolled 45 participants across 65 sites in 15 countries.

Detailed Summary

This is a Phase 3, multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of imsidolimab compared with placebo in adult subjects with generalized pustular psoriasis (GPP).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, France, Georgia, Germany, Malaysia, Morocco, Poland, Romania, South Korea, Spain, Taiwan, Thailand, Tunisia, Turkey (Türkiye), United States
Collaborators--

Timeline

Phase 3CompletedFinished
2023202420252026
First PostedApr 29, 2022
Enrollment StartApr 14, 2022
Primary CompletionAug 17, 2023
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 4.2 years ago

Interventions

750 mg Imsidolimabdrug

Intravenous

300 mg Imsidolimabdrug

Intravenous

Placeboother

Intravenous