Trial intelligence / Profile preview

Safety and Pharmacokinetics of REGN9035 and Vixticibart in Healthy and Hypertensive Subjects

NCT05291546Phase 1Completed

Sponsor
Regeneron Pharmaceuticals
Start
Apr 2022
Primary completion
Apr 2024
Modality
Monoclonal Antibodies
Countries
2
01

Overview

Phase 1, randomised, double-blind trial in hypertension (HTN) comparing Part A: REGN9035 SAD with Part B: Vixticibart + REGN9035 (2 arms). Primary endpoint: Treatment Emergent Adverse Events. Started Apr 2022; status: completed.

02

Drugs

REGN5381imelciment
03

Conditions

hypertension (HTN)

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