Phase 2 Cardiomyopathy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People between 40 and 80 years old.
- People who have heart failure with a weakened heart pump (where the heart is pumping less blood than normal), caused either by blocked arteries or other reasons, confirmed by a heart scan showing the pumping function is below 40%.
- People who have a heart condition caused by a protein build-up called ATTR cardiomyopathy, with any level of heart pumping function confirmed by a heart scan.
- People whose heart failure medicines have been stable and at the best tolerated doses for at least 3 months, with no changes to their treatment for at least 1 month.
- People with a specific blood marker level (NT-proBNP) above a certain threshold — above 125 pg/mL for those under 75 years old, or above 450 pg/mL for those 75 and older.
Who may not be able to join:
- People who have had a heart procedure (such as a stent or bypass) in the past 3 months.
- People who are pregnant.
- People who have endometriosis (a condition where tissue similar to the uterine lining grows outside the uterus).
- People who have uterine fibroids (non-cancerous growths in the uterus).
- People with a current cancer diagnosis, including breast cancer, an abnormal mammogram result, a family history of cancer, or who carry the BRCA1 or BRCA2 gene variants.
- People who follow a vegan diet.
- People who take supplements such as isoflavonoids, genistein, or resveratrol.
- People with alcohol use concerns — for men, this means drinking more than 4 drinks on any single day or more than 14 drinks per week; for women, more than 3 drinks on any single day or more than 7 drinks per week.
- People with liver problems, where certain liver function blood test results are significantly above the normal range (confirm specific values with the trial site).
- People currently taking hormone replacement therapy (HRT).
- People currently taking thyroid supplements.
- People with significantly reduced kidney function (eGFR below 25 mL/min/1.73 m²) (confirm with trial site).
- People with poorly controlled diabetes, where a blood sugar marker (HbA1c) is above 10%.
- People with blood clotting disorders.
- People with certain low blood cell counts, including low white blood cells, haemoglobin below 9 mg/dL, or low platelets.
- People who have been hospitalised in the past 3 months for any reason other than heart failure.
- People whose heart failure symptoms fall into the mildest category (no symptoms at all) or the most severe category (symptoms even at rest), based on a standard heart failure classification system.
- People with an active bacterial or viral infection, or a flare-up of a long-term infection.
- People with a known allergy to genistein or inulin.
- People with a known allergy to perflutren dye, which is used in certain heart ultrasound scans.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Mark JK Chandy, MD PhD, Lawson
Phone: 5196612111
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Inflammatory markers; Cardiac markers; Complete metabolic profile
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.