drugset / Trial / NCT07695090

Lumacaftor Yields Reversal of Impaired Cerebral Blood Flow in Heart Failure Patients

NCT07695090

Phase 2 Recruiting 60 enrolled Qanatpharma AG Qanatpharma Canada LTD · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

Cognitive impairment (CI) is highly prevalent in patients with heart failure with reduced ejection fraction (HFrEF), which has significant implications for disease management, quality of life and clinical outcomes. Currently, there are no specific treatments for CI aside from the current standard of care therapy for HF, making this a high unmet medical need. Impaired cerebral autoregulation is a proposed mechanistic factor that leads to cerebral hypoperfusion, ischemic damage and the development for CI. Preclinical data indicates that restoring CFTR-protein expression normalizes cerebral microvascular function and cerebral blood flow (CBF) in models of HF. The purpose of this study is to investigate whether CFTR-targeting therapy enhances cerebral perfusion and cognitive function in heart failure patients using the CFTR-corrector Lumacaftor.

Timeline

Start
2026-07
Primary completion
2027-05
Completion
2027-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Lumacaftor Small molecule 200 mg