Genistein in trAnSthyretin recePtor Amyloid caRdiomyopathy

Recruiting Phase 1 Phase 2 Interventional Study
Amyloid Cardiomyopathy
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
40 – 80
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Other
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About This Trial
This Phase 1b/2a study aims to investigate the safety and efficacy of genistein in patients with Transthyretin (TTR) Amyloidosis. The focus is on its impact on inflammatory and cardiometabolic biomarkers, along with the effects on cardiac function and exercise capacity. Blood samples will be collected at baseline, following each dose of genistein, and after a six-week placebo washout period. Thes…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age: 40-80 years * Heart failure with Reduced Ejection Fraction * ischemic or nonischemic etiology * LVEF \<40% by echocardiography, MUGA, or MRI * ATTR cardiomyopathy * any LVEF by echocardiography, MUGA, or MRI * Stable optimally tolerated dosages of HF therapies for…
Contacts

Mark JK Chandy, MD PhD

5196612111

mark.chandy@lhsc.on.ca

CONTACT

Kerry-Ann Nakrieko, PhD

5196112111

knakrie@uwo.ca

CONTACT