Pulmonary Hypertension clinical trials at UC Irvine

4 in progress, 2 open to eligible people

Showing trials for

  • Learn About the Treatment LTP001 in Healthy Participants (Part A) and in Participants With PAH (Part B)

    open to eligible people ages 18-100

    A study to learn about the treatment LTP001 in healthy participants (Part A) and in participants with PAH (Part B)

    Orange, California and other locations

  • De-implementing Inhaled Nitric Oxide for Congenital Diaphragmatic Hernia

    open to eligible people ages 0 months to 1 month

    The purpose of this study is to determine if de-implementation of inhaled nitric oxide (iNO) in the post-natal resuscitation/stabilization phase affects the composite outcome of extracorporeal life support (ECLS) use and/or mortality, as well as ECLS use, mortality, and/or oxygenation in congenital diaphragmatic hernia (CDH) newborns and to establish the cost-effectiveness of de-implementing iNO as a therapy in the postnatal resuscitation/stabilization phase of CDH management, which will be assessed as the incremental health system costs (savings) per prevented ECLS use and/or death.

    Irvine, California and other locations

  • Long-Term Efficacy and Safety of Ralinepag in Subjects With PAH Via an Open-Label Extension

    Sorry, accepting new patients by invitation only

    Study ROR-PH-303, ADVANCE EXTENSION, is an open-label extension (OLE) study for participants with WHO Group 1 PAH who have participated in another Phase 2 or Phase 3 study of ralinepag.

    Orange, California and other locations

  • Learn About the Study Medicine Called PF-07868489 in Healthy Adult People and in People With Pulmonary Arterial Hypertension

    Sorry, in progress, not accepting new patients

    The purpose of the study is to learn how the study medicine called PF-07868489 is tolerated and acts in healthy adult people and people with pulmonary arterial hypertension (PAH). Part A: An investigator- and participant-blind, sponsor-open, placebo-controlled, single ascending dose study to assess the safety, tolerability, and pharmacokinetics (PK) of PF-07868489 in healthy adult participants. Part B: A 24-week, randomized, double blind, placebo-controlled study to assess the safety, tolerability, PK, and pharmacodynamics (PD) of PF-07868489 in adult participants with PAH.

    Orange, California and other locations

Our lead scientists for Pulmonary Hypertension research studies include .

Last updated: