Phase 2 Cardiomyopathy Trial, Recruiting NCT06902896 Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University Condition: Cardiomyopathy
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Phase 2 Cardiomyopathy Trial, Recruiting

NCT06902896
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 aged between 18 and 75 years old who have been diagnosed with dilated cardiomyopathy (a condition where the heart muscle is weakened and enlarged).
  • People who are able to confirm they understand the risks, benefits, and treatment options involved, and who (or whose legal representative) are willing to sign a consent form before taking part.
  • People diagnosed with heart failure where the heart's pumping function is significantly reduced, who have been on the maximum tolerated standard heart failure medications for at least 3 months, whose heart pumps less than 35% of its capacity, and whose symptoms fall within a specific range of severity (NYHA class IIIB–IV and INTERMACS class 3–6) (confirm with trial site).
  • People whose blood test results show: red blood cell levels (hematocrit) above 30%, a type of white blood cell (lymphocytes) above a certain level, and platelets above a certain level (confirm exact values with trial site).

Who may not be able to join:

  • People who have had a heart attack, unstable chest pain, stroke, or a mini-stroke (transient ischemic attack) within the 12 weeks before enrolling.
  • People who have had a cardiac resynchronisation therapy (CRT) device implanted within the 12 weeks before enrolling, or who are planning to have one implanted.
  • People who have previously had a heart transplant or a mechanical heart pump device implanted, or who are planning to have one.
  • People whose heart failure is caused by conditions other than dilated cardiomyopathy, such as blocked arteries, stiff heart muscle, active heart inflammation, scarring around the heart, thickened heart muscle, long-term high blood pressure, birth-related heart defects, or uncorrected valve disease.
  • People who have a dangerously slow heart rate with symptoms, or a significant electrical conduction problem in the heart (second or third degree heart block).
  • People who have an active autoimmune disease that currently requires medication to suppress the immune system.
  • People who have a blood clot in the lungs (pulmonary embolism).
  • People with a history of tuberculosis.
  • People with a history of severe kidney failure or who require dialysis, or whose creatinine (a measure of kidney function) is above a certain level.
  • People with uncontrolled low platelet counts or blood clotting problems, or who have active bleeding that cannot be corrected.
  • People with significantly elevated liver enzyme levels or raised bilirubin (a marker of liver function) in their blood.
  • People with a history of serious ongoing infection, blockage in the liver or bile ducts, or cancer.
  • People with active hepatitis B (at a certain level of virus detected in the blood), hepatitis C, syphilis, or HIV; or any uncontrolled serious infection caused by fungus, bacteria, a virus, or another pathogen.
  • People in a state of severe haemodynamic instability, such as shock (where the body's organs are not receiving enough blood).
  • People who are pregnant or who may become pregnant during the trial.
  • People who have known contraindications (reasons they should not receive) to any of the study drugs or tests involved.

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: Xinyang Hu, PhD, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Phone: 86-18868112006

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
22 April 2025
Est. completion
30 June 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The proportion of subjects with Dose-limiting toxicity (DLT); Incidence of treatment-emergent adverse events (TEAEs)

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