drugset / Trial / NCT03532958
Phase 2 Trial of BNZ-1 in Patients With Moderate to Severe Alopecia Areata
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This study is a randomized, double-blind, placebo-controlled, multi-center, dose-ranging study to characterize the efficacy and safety of BNZ-1 administered by slow IV push weekly for 3 months to adults diagnosed with moderate to severe alopecia areata, defined as having a \>50% loss of terminal hair on the scalp. The study has three periods: * 30-Day Screening Period * 3-Month Treatment Period * 3-Month Follow-up Period The study will be conducted at approximately 15-20 clinical sites in the United States.
Timeline
- Start
- 2021-10
- Primary completion
- 2022-11
- Completion
- 2022-11
Outcome
Outcome not reported
Stopped: “Transfer of study sponsor”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BNZ-1 | Peptide | 0.5 mg/kg | Intravenous |
| Subject | BNZ-1 | Peptide | 2 mg/kg | Intravenous |