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A Study to Investigate the Safety and Efficacy of KER-012 in Combination With Background Therapy in Adult Participants With Pulmonary Arterial Hypertension (PAH) (TROPOS). - Trial NCT05975905

Access comprehensive clinical trial information for NCT05975905 through Pure Global AI's free database. This Phase 2 trial is sponsored by Keros Therapeutics, Inc. and is currently Recruiting. The study focuses on Pulmonary Arterial Hypertension. Target enrollment is 90 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT05975905
Phase 2
Recruiting
biological
Trial Details
ClinicalTrials.gov โ€ข NCT05975905
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A Study to Investigate the Safety and Efficacy of KER-012 in Combination With Background Therapy in Adult Participants With Pulmonary Arterial Hypertension (PAH) (TROPOS).
A Randomized, Phase 2, Double-blind, Placebo-controlled Study to Investigate the Safety and Efficacy of KER-012 in Combination With Background Therapy in Adult Participants With Pulmonary Arterial Hypertension (TROPOS)

Study Focus

Dose A KER-012

Interventional

biological

Sponsor & Location

Keros Therapeutics, Inc.

Sydney, Australia

Timeline & Enrollment

Phase 2

Jun 27, 2023

Jan 31, 2027

90 participants

Primary Outcome

Change from Baseline in PVR (Pulmonary Vascular Resistance)

Summary

Study KER-012-A201 is Phase 2, double-blind, randomized, placebo-controlled study to
 determine the efficacy and safety of KER-012 compared to Placebo in adults with PAH (WHO
 Group 1 PH) on stable background PAH therapy. The study is divided into the Screening Period,
 Treatment Period, Extension Period, and Follow-Up Period.

ICD-10 Classifications

Primary pulmonary hypertension
Other secondary pulmonary hypertension
Pulmonary heart disease and diseases of pulmonary circulation
Stenosis of pulmonary artery
Pulmonary heart disease, unspecified

Data Source

ClinicalTrials.gov

NCT05975905

Non-Device Trial