drugset / Trial / NCT04503733

A Study of GMA301 in Subjects With Pulmonary Arterial Hypertension

NCT04503733 ↗

Phase 1 Unknown 48 enrolled Gmax Biopharm LLC.
RandomizedSequentialDouble-blindTreatment

Summary

A Randomized, Placebo-Controlled, Double-blind, Dose Escalation Study to Assess Safety, Efficacy and Pharmacokinetics of GMA301 Injection in Subjects with Pulmonary Arterial Hypertension

Timeline

Start
2020-10-22
Primary completion
2022-10-26
Completion
2023-06-10

Drugs

EvaluationDrugModalityDoseRoute
Subject PATECIBART Monoclonal antibody 300 mg Intravenous
Subject PATECIBART Monoclonal antibody 600 mg Intravenous
Subject PATECIBART Monoclonal antibody 1000 mg Intravenous
Subject PATECIBART Monoclonal antibody 1800 mg Intravenous