Trial Profile

A Phase 2b, Double-Blind, Randomized, Placebo-Controlled, Dose-Finding Study, to Compare the Efficacy and Safety/Tolerability of CS1 Versus Placebo When Added to Standard of Care for the Treatment of Pulmonary Arterial Hypertension (PAH).

Status: Planning

Phase of Trial: Phase II

Latest Information Update: 18 Dec 2025

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At a glance

18 Dec 2025 New trial record
08 Dec 2025 According to the Cereno Scientific media release, the U.S. Food and Drug Administration (FDA) has granted clearance to initiate the company's Phase IIb trial of its lead drug candidate CS1 for the treatment of pulmonary arterial hypertension (PAH). First patient in (FPI) is planned for Q2 2026, with top-line results anticipated around Q4 2028, subject to enrollment timelines.

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