CIRRUS-HCM (Hypertrophic Cardiomyopathy) - Clinical Trial

What is the Purpose of this Study?

We are doing this study to find out if an experimental drug called EDG-7500 (the study drug) is a safe and effective option for patients with both obstructive and non-obstructive hypertrophic cardiomyopathy (HCM).

The study drug is designed to help the heart's ability to relax by making contractions more controlled, and we want to know how successful the drug is in achieving its intended outcome.

What is the Condition Being Studied?

Obstructive or Non-obstructive Hypertrophic Cardiomyopathy (HCM)

Who Can Participate in the Study?

Adults ages 18+ who:

  • Have a body mass index (BMI) that is less than 38 kg/m2
  • Have a left ventricular ejection fraction of at least 60%
  • Have New York Heart Association (NYHA) Classification I-III HCM at the start of the study
  • Have not had any changes to their dosing within 30 days of joining the study if they use a beta blocker

For more information, contact the study team at joshua.stablein@duke.edu.

Grupo etario
Adultos

What is Involved?

If you choose to join this study, you will participate in 1 of 4 different parts to the study:

  • Part A (lasts about 2-6 weeks): In this part, you will be screened for eligibility, have a single clinic visit to get the study drug, and have follow-up visits with the study team. You will get only one dose of the study drug.
  • Part B & Part C (each lasts about 2.5 months): In this part, you will be screened for eligibility, take the study drug every day for 28 days at home, and have follow-up visits with the study team.
  • Part D (lasts about 12.5 months): In this part, you will be screened for eligibility, take the study drug every day for 48 weeks at home, and have follow-up visits with the study team.

Procedures during your study visits will include physical exams, genetic testing, blood draws, heart function tests (ECG, echocardiograms), and symptom assessments. Some tests, like stress tests, are optional.

If you take part in Part A, you will get a random assignment to be placed into 1 of several groups that will get different doses of the study drug. Neither you nor the study team can choose your group assignment, but we will let you know what it is.

Study Details

Full Title
An Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of EDG-7500 in Adults with Hypertrophic Cardiomyopathy
Principal Investigator
Especialista en enfermedad estructural del corazón
Protocol Number
IRB: PRO00117443
NCT: NCT06347159
Phase
Phase II
ClinicalTrials.gov
Estado de inscripción
Abierto para inscripción
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