Familial primary pulmonary hypertension

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Information
Disease name
Familial primary pulmonary hypertension
Disease ID
Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT03528902 Completed Phase 2 Tamoxifen Therapy to Treat Pulmonary Arterial Hypertension October 1, 2018 June 14, 2023
NCT04908397 Completed Phase 1 Carnitine Consumption and Augmentation in Pulmonary Arterial Hypertension September 29, 2021 June 30, 2023
NCT03683186 Enrolling by invitation Phase 3 A Study Evaluating the Long-Term Efficacy and Safety of Ralinepag in Subjects With PAH Via an Open-Label Extension September 23, 2019 September 2024
NCT03626688 Recruiting Phase 3 A Study Evaluating the Efficacy and Safety of Ralinepag to Improve Treatment Outcomes in PAH Patients August 30, 2018 December 2024
NCT04084678 Terminated Phase 3 A Study of Ralinepag to Evaluate Effects on Exercise Capacity by CPET in Subjects With WHO Group 1 PH January 20, 2021 April 12, 2023
NCT01645826 Withdrawn N/A Efficacy Study of Cardizem in Pulmonary Arterial Hypertension July 2012 September 2014
MedGen concept unique identifier (MedGen Concept name)
C0340543
MedGen unique identifier (MedGen Concept name)
90953
MeSH unique ID (MeSH (Medical Subject Headings))
D065627