Trial intelligence / Profile preview

Safety and PK of High-Dose GMA301 in Healthy Volunteers

NCT04505137Phase 1Completed

Sponsor
Gmax Biopharm
Start
Sep 2020
Primary completion
Mar 2021
Modality
Engineered Antibody Formats, Antibody Conjugates, Monoclonal Antibodies
Countries
1
01

Overview

Phase 1, randomised, double-blind trial of GMA301 in pulmonary arterial hypertension (PAH) (2 cohorts), sponsored by Gmax Biopharm. Primary endpoint: Safety and Tolerability (Adverse Events) at Day 70. Started Sep 2020; status: completed.

02

Drugs

GMA301
03

Conditions

pulmonary arterial hypertension (PAH)

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