drugset / Trial / NCT05934526
Efficacy and Safety of Seralutinib in Adult Subjects With PAH (PROSERA)
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary objective of the study is to determine the effect of seralutinib on improving exercise capacity in subjects with WHO Group 1 PAH who are FC II or III. The secondary objective for this trial is to determine time to clinical worsening.
Timeline
- Start
- 2023-12-28
- Primary completion
- 2025-11-27
- Completion
- 2025-12-22
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Seralutinib | Peptide | 90 mg | Inhaled |