drugset / Trial / NCT07641634
A Phase 1/2 Study of PRO-203 in Healthy Volunteers and Participants With Systemic Sclerosis.
RandomizedSequentialTriple-blindTreatment
Summary
A two-part study of PRO-203 administered subcutaneously in healthy adult volunteers and participants with Systemic Sclerosis (SSc).
Timeline
- Start
- 2025-10-27
- Primary completion
- 2027-01
- Completion
- 2028-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PRO-203 | Unknown | — | Subcutaneous |