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Clinical Trial ● Currently Recruiting Phase II NCT06814145

Extension Study of Sotatercept in People With Pulmonary Hypertension (MK-7962-023)

Extension Study of Sotatercept in People With Pulmonary Hypertension (MK-7962-023) — Recruiting • Phase II • Cardiology / Cardiovascular • NCT06814145.

📅 27 Mar 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT06814145
Sponsor
Merck Sharp & Dohme LLC
Start
2025-04-16
ClinicaliQ Trial Snapshot
  • Extension Study of Sotatercept in People With Pulmonary Hypertension (MK-7962-023) — Recruiting • Phase II • Cardiology / Cardiovascular • NCT06814145.
  • Researchers are looking for new ways to treat people with a type of pulmonary hypertension called combined postcapillary and precapillary pulmonary hypertension (Cpc-PH). This study focuses on Cpc-PH that is caused by heart failure with preserved ejection fraction (HFpEF). Researchers want to….
  • Sponsor: Merck Sharp & Dohme LLC.

Verify eligibility, endpoints and current status on the original source registry before acting on this summary.

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  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

Researchers are looking for new ways to treat people with a type of pulmonary hypertension called combined postcapillary and precapillary pulmonary hypertension (Cpc-PH). This study focuses on Cpc-PH that is caused by heart failure with preserved ejection fraction (HFpEF). Researchers want to know if the study treatment, sotatercept, can treat people with Cpc-PH caused by HFpEF. This is an extension study, which means people who took part in a certain study on sotatercept for Cpc-PH (called a parent study) may be able to join this study. In this extension study,…

Eligibility Snapshot
  • : The main inclusion criteria include but are not limited to the following: - Completed MK-7962-007 (CADENCE) (Visit 9 and end of treatment [EOT] visit) without discontinuing study intervention and is able to safely enroll into MK-7962-007 (HARMONIZE)

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
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Eligibility criteria, protocol, and results when available
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Related Clinical Intelligence

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