drugset / Trial / NCT05470413

Evaluate the Efficacy and Safety of SHR0302 in Adult Patients With Severe Alopecia Areata

NCT05470413

Phase 3 Unknown 330 enrolled Reistone Biopharma Company Limited
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multi-central, double-blind, randomized, parallel, placebo-controlled phase 3 study in adult subjects with severe alopecia areata (SALT≥50%). Approximately 330 adult patients will be enrolled into the study. Efficacy and safety of two doses of SHR0302 will be compared to placebo.

Timeline

Start
2022-04-18
Primary completion
2023-10-31
Completion
2024-02-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator SHR0302 Unknown 4 mg
Comparator SHR0302 Unknown 8 mg

Indications