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Clinical Trials in the EU / 2024-514754-79-00
Ongoing Phase II

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamic Effects of REGN13335, an Anti-PDGF-B Monoclonal Antibody, in Adults with Pulmonary Arterial Hypertension

2024-514754-79-00 · tracked via the Priya Life Science EU tracker
Sponsor
Regeneron Pharmaceuticals Inc.
Sponsor type
Pharmaceutical company
Therapeutic area
Cardiovascular Diseases
Decision date
18/03/2026
Enrollment target
47
Sites
Latvia, Belgium, France, Poland, Germany, Spain, Czechia

Condition studied

Pulmonary Arterial Hypertension (PAH)

Investigational medicinal product(s)

REGN13335REGN13335Placebo to REGN13335

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

Change from baseline in Pulmonary Vascular Resistance (PVR)

Endpoint detail

Occurrence of Treatment-Emergent Adverse Events (TEAEs), Severity of TEAEs, Change from baseline in circulating N-Terminal pro-B-type Natriuretic Peptide (NT-proBNP) concentrations, Change from baseline in mean pulmonary artery pressure, Change from baseline in cardiac output, Change from baseline in cardiac index, Change from baseline in right atrial pressure, Change from baseline in 6-Minute Walk Distance (6MWD), Concentrations of functional REGN13335 in plasma, Concentrations of total soluble Platelet-Derived Growth Factor-B (PDGF-B) ligands in plasma

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2024-514754-79-00 on CTIS ↗ ← All trials in the EU