Repurposing Valsartan May Protect Against Pulmonary Hypertension

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is a Phase 2, single-center, randomized placebo controlled trial of valsartan (an angiotensin receptor blocker) in adults with pulmonary arterial hypertension. The study will evaluate the safety and clinical efficacy of a 24-week course of valsartan.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Male or female, age 18 to 80

• WHO Group 1 Pulmonary Arterial Hypertension

• NYHA Functional Class II, III, or IV at screening (Appendix 2 for Functional Class Decision Aid)

• Right heart catheterization within five years demonstrating a mean pulmonary arterial pressure of ≥25 mmHg, occlusion pressure of ≤15 mmHg, and resistance ≥ 3 wood units

• Participants with a right heart catheterization within five years demonstrating a mean pulmonary arterial pressure of ≥ 25 mmHg and occlusion pressure of 15 - 20 mmHg will be considered for inclusion if the pulmonary vascular resistance ≥ 9 wood units and they are being treated with pulmonary arterial hypertension specific therapy

• Able to walk with/without a walking aid for a distance of at least 50 meters

Locations
United States
Washington
University of Washington Medical Center
RECRUITING
Seattle
Contact Information
Primary
Laurie Hogl, RRT
lalnaser@uw.edu
206.543.8334
Backup
Nancy Liston, MS
nmliston@uw.edu
206.543.8334
Time Frame
Start Date: 2024-02-28
Estimated Completion Date: 2027-07-01
Participants
Target number of participants: 60
Treatments
Experimental: Valsartan
Valsartan 40mg capsule taken twice daily for 24 weeks.
Placebo_comparator: Placebo
Placebo capsule taken twice daily for 24 weeks.
Sponsors
Leads: University of Washington
Collaborators: National Heart, Lung, and Blood Institute (NHLBI)

This content was sourced from clinicaltrials.gov