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GMA-301

Alternative Names: gma-301, gma 301, gma301, GMA-301a, GMA-301b
Latest Update: 2022-01-14
Latest Update Note: Clinical Trial Update

Product Description

GMA301 is a humanized monoclonal antibody against endothelin receptor A, may become the first long-lasting PAH drug with better efficacy and less adverse effects. (Sourced from: https://www.gmaxbiopharm.com/wap_product_detailen/id/4.html)

Mechanisms of Action: ETa Inhibitor

Novel Mechanism: No

Modality: Antibody

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Gmax Biopharm
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for GMA-301

Countries in Clinic: China

Active Clinical Trial Count: 1

Highest Development Phases

Phase 1: Hypertension, Pulmonary

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

CTR20200854

P1

Not yet recruiting

Hypertension, Pulmonary

None

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