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 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.
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
Where this trial is recruiting
Primary endpoints
The proportion of subjects with Dose-limiting toxicity (DLT); Incidence of treatment-emergent adverse events (TEAEs)
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.