Phase 2 Cardiomyopathy Trial, Recruiting NCT06634108 Sponsor: London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's Condition: Cardiomyopathy
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Phase 2 Cardiomyopathy Trial, Recruiting

NCT06634108
Recruiting Phase 2

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
27 September 2024
Est. completion
1 September 2025

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Inflammatory markers; Cardiac markers; Complete metabolic profile

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov