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A Randomized, Double-Blind, Parallel Group, Phase 2 Study to Assess the Safety, Tolerability, and Efficacy of Once Weekly Subcutaneous (SC) Injections of a Sustained-Release Vasoactive Intestinal Peptide (VIP) Analogue, Pemziviptadil (PB1046), in Adult Subjects With Symptomatic Pulmonary Arterial Hypertension (PAH)

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Trial Profile

A Randomized, Double-Blind, Parallel Group, Phase 2 Study to Assess the Safety, Tolerability, and Efficacy of Once Weekly Subcutaneous (SC) Injections of a Sustained-Release Vasoactive Intestinal Peptide (VIP) Analogue, Pemziviptadil (PB1046), in Adult Subjects With Symptomatic Pulmonary Arterial Hypertension (PAH)

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 13 Sep 2023

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At a glance

  • Drugs Pemziviptadil (Primary)
  • Indications Pulmonary arterial hypertension
  • Focus Adverse reactions; Pharmacodynamics; Therapeutic Use
  • Acronyms VIP
  • Sponsors PhaseBio Pharmaceuticals

    • Most Recent Events

    • 04 Feb 2022 Status changed from suspended to discontinued. Reason the study was stopped: Terminated: Study drug resupply delayed (Covid-19).
    • 19 Jan 2022 This trial has been discontinued in Austria (Date of the global end of the trial : 22-Dec-2021), according to European Clinical Trials Database record.
    • 13 Jan 2022 This trial has been discontinued in Hungary, according to European Clinical Trials Database (22 Dec 2021)
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