drugset / Trial / NCT05934526

Efficacy and Safety of Seralutinib in Adult Subjects With PAH (PROSERA)

NCT05934526 ↗

Phase 3 Completed 390 enrolled GB002, Inc.
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

EvaluationDrugModalityDoseRoute
Subject Seralutinib Peptide 90 mg Inhaled