Phase 1 Cardiomyopathy Trial, Recruiting NCT02962661 Sponsor: M.D. Anderson Cancer Center Condition: Cardiomyopathy
Back to Cardiomyopathy

Phase 1 Cardiomyopathy Trial, Recruiting

NCT02962661
Recruiting Phase 1

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:

  • You have a weakened heart (reduced pumping ability of 40% or less) that was caused by chemotherapy drugs called anthracyclines, used to treat any type of cancer, at any dose and at any point in the past, with no other known cause for the heart weakness.
  • You are between 18 and 90 years old. Both English and non-English speakers are welcome.
  • Your heart failure symptoms have been classified by a doctor as mild, moderate, or noticeable but not severe (NYHA Class I, II, or III — confirm with trial site if unsure which applies to you).
  • If you were also treated with the drug trastuzumab (Herceptin), your heart must still be showing weakness at least 90 days after stopping that treatment.
  • You are able to complete a 6-minute walking test.
  • You have already been treated with the best available standard medicines for heart failure.
  • You, or someone legally authorised to act on your behalf, are able to sign a consent form.

Who may not be able to join:

  • You have been diagnosed with heart disease caused by blocked or narrowed arteries, as confirmed by a heart specialist.
  • You have a significant heart valve problem (such as a severely narrowed or leaking valve — confirm with trial site).
  • You have a family history of inherited heart muscle disease.
  • You have had heart muscle inflammation (myocarditis) within the past 2 months.
  • You have a history of heart muscle disease caused by a substance building up in the heart, or a stiffening of the heart muscle (confirm with trial site).
  • A blood clot has been found inside the left side of your heart, as shown by a heart scan.
  • Your liver is not functioning well — specifically, certain liver test results are more than 3 times higher than the normal range.
  • Your heart failure symptoms are classified as very severe (NYHA Class IV — confirm with trial site).
  • You rely on medication given through a drip to keep your heart pumping.
  • You have a dangerous or unstable irregular heartbeat.
  • If you are not taking blood-thinning medication, your blood clotting level (INR) is above 1.5 (confirm with trial site).
  • You have an artificial or donor tissue heart valve.
  • Your heart is in a state of crisis and cannot pump enough blood to the body (cardiogenic shock).
  • You are currently pregnant or breastfeeding.
  • You have an autoimmune condition and are currently taking medication that suppresses your immune system.
  • You have an active infection that is not responding to treatment, as assessed by the trial doctor.
  • You have received trastuzumab (Herceptin) within the last 3 months.
  • You have had an internal heart defibrillator device (AICD) implanted within the last 30 days.
  • Your internal heart defibrillator (AICD) has delivered a shock within the last 30 days.

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 27 July 2026
Phase 1: approximately ~10% 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: Amanda Olson, MD, M.D. Anderson Cancer Center

Phone: 713-745-3055

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 1
Registry
ClinicalTrials.gov
Start date
18 July 2020
Est. completion
30 July 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of adverse events; Change in left ventricular ejection fraction (LVEF)

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: 27 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