drugset / Trial / NCT06857955

A Study to Identify an Optimal Dose of QCZ484 in Mild to Moderate Hypertensive Patients

NCT06857955

Phase 2 Active not recruiting 399 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupTriple-blindOther

Summary

The purpose of this study is to evaluate the efficacy, safety and tolerability of QCZ484 or placebo, given subcutaneously, every 6 months, at different dose levels in patients with mild to moderate hypertension

Timeline

Start
2025-03-26
Primary completion
2027-01-29
Completion
2028-04-05

Drugs

EvaluationDrugModalityDoseRoute
Subject QCZ484 Unknown Subcutaneous

Indications