Drug intelligence / Profile preview

zelminemab

Development stage
Phase 2
Lead developer
Amgen
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Subcutaneous
01

Overview

Zelminemab (AMG 301) is a fully human monoclonal antibody developed for the prevention of migraine. It acts as an antagonist of the pituitary adenylate cyclase-activating polypeptide type I (PAC1) receptor. By inhibiting this receptor, which is implicated in migraine pathophysiology through neuronal signaling pathways, zelminemab was intended to reduce migraine frequency and severity. Clinical trials demonstrated that it did not provide significant benefit over placebo in reducing monthly migraine days or other efficacy measures[2][4][5]. The drug was originally developed by Amgen and later licensed to Novartis for markets outside the USA, Canada, and Japan[4].

Other names
zelminemabAMG 301AMG301AMG-301
02

Targets

ADCYAP1R1 (Pituitary adenylate cyclase-activating polypeptide receptor PAC1)

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