RecruitingPhase 2NCT07073820

A Study to Learn About the Study Medicine (Called PF-07868489) in People With Pulmonary Arterial Hypertension Who Have Previously Participated in a Clinical Study With PF-07868489

A PHASE 2, OPEN-LABEL EXTENSION STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF PF-07868489 ADMINISTERED TO ADULT PARTICIPANTS WITH PULMONARY ARTERIAL HYPERTENSION


Sponsor

Pfizer

Enrollment

36 participants

Start Date

Nov 10, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to learn about the long-term safety, tolerability and effects of the study medicine (PF-07868489) for the possible treatment of PAH. PAH is a condition in which there is high blood pressure in the arteries that carry blood from the heart to the lungs. This high pressure makes it harder for the heart to pump blood through those lungs, potentially damaging the right side of the heart. This is an open-label study. Which means that both the healthcare providers and the study participants are aware of the medicine being given. This study is also an extension study with study medicine (PF-07868489). An extension study allows patients from an earlier clinical study (also called as qualifying study) to continue participating to assess long-term benefits and safety of the medicine.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is offering continued access to an investigational drug called PF-07868489 for people with pulmonary arterial hypertension (a type of high blood pressure in the lungs) who have already been part of a previous study with this drug. **You may be eligible if...** - You previously took part in a clinical study with PF-07868489 and completed the full required treatment period - You are 18 years or older at the time you enrolled in the original study - You are willing to follow all scheduled visits, tests, and study procedures **You may NOT be eligible if...** - You were hospitalized for worsening pulmonary arterial hypertension during the prior study - You are on a waiting list for or planning to have a transplant or PAH surgery - You had a major health issue during the qualifying study that the doctor believes would disqualify you - You have a history of a condition called hepato-pulmonary syndrome Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPF-07868489

Participants will receive subcutaneous doses of PF-07868489 every 4 weeks


Locations(44)

UCSF Health St. Mary's Hospital

San Francisco, California, United States

Heart and Vascular Center

San Francisco, California, United States

University of Colorado Anschutz Medical Campus

Aurora, Colorado, United States

Norton Hospital

Louisville, Kentucky, United States

Norton Pulmonary Specialists

Louisville, Kentucky, United States

Clinical Trials Unit at Eastowne Medical Office Building

Chapel Hill, North Carolina, United States

Pulmonary Hypertension Clinical Trials Office at Eastowne

Chapel Hill, North Carolina, United States

Pulmonary Specialty Clinic at Eastowne Medical Office Building

Chapel Hill, North Carolina, United States

UNC Hospitals

Chapel Hill, North Carolina, United States

Rhode Island Hospital

Providence, Rhode Island, United States

Center for Advanced Lung Care

Providence, Rhode Island, United States

Royal Prince Alfred Hospital

Camperdown, New South Wales, Australia

Pulmonary Hypertension Research Queensland Pty Ltd

Auchenflower, Queensland, Australia

HUB Hôpital Erasme

Brussels, Belgium

UZ Leuven

Leuven, Belgium

London Health Sciences Centre - University Hospital

London, Ontario, Canada

London Health Sciences Centre

London, Ontario, Canada

Guangdong Provincial People's Hospital

Guangzhou, Guangdong, China

The Second Xiangya Hospital of Central South University

Changsha, Hunan, China

Zhongda Hospital Southeast University

Nanjing, Jiangsu, China

Shanghai Pulmonary Hospital

Shanghai, Shanghai Municipality, China

Vseobecna fakultni nemocnice v Praze

Prague, Czechia

CHRU de Brest

Brest, Finistère, France

Centre Hospitalier Universitaire de Saint-Etienne, Hôpital Nord

Saint-Priest-en-Jarez, France

Thoraxklinik-Heidelberg gGmbH

Heidelberg, Baden-Wurttemberg, Germany

Universitätsklinikum Regensburg

Regensburg, Bavaria, Germany

Universitaetsklinikum Giessen und Marburg GmbH

Giessen, Hesse, Germany

Universitätsmedizin Greifswald

Greifswald, Mecklenburg-Vorpommern, Germany

Universitaetsklinikum Carl Gustav Carus, Technischen Universitaet Dresden

Dresden, Saxony, Germany

University General Hospital "ATTIKON" - General Hospital of West Attica "H AGIA VARVARA"

Chaïdári, Attica, Greece

AHEPA University General Hospital of Thessaloniki

Thessaloniki, Central Macedonia, Greece

Fondazione IRCCS Policlinico San Matteo

Pavia, Italy

Kobe University Hospital

Kobe, Hyōgo, Japan

St. Marianna University Hospital

Kawasaki, Kanagawa, Japan

Tohoku University Hospital

Sendai, Miyagi, Japan

National Hospital Organization Okayama Medical Center

Okayama, Japan

Gachon University Gil Medical Center

Incheon, Incheon-gwangyeoksi [incheon], South Korea

Seoul National University Hospital

Seoul, Seoul-teukbyeolsi [seoul], South Korea

Severance Hospital, Yonsei University Health System

Seoul, Seoul-teukbyeolsi [seoul], South Korea

Samsung Medical Center

Seoul, Seoul-teukbyeolsi [seoul], South Korea

Hospital Universitario Marques de Valdecilla

Santander, Cantabria, Spain

Hospital Universitario La Paz

Madrid, Madrid, Comunidad de, Spain

Hospital Universitario 12 de Octubre

Madrid, Spain

Hammersmith Hospital

London, Greater London, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT07073820


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