Rocket RP-NI-A501-0223 (Danon NHS)
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StatusAccepting Candidates
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Age8 Years - N/A
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SexesAll
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Healthy VolunteersNo
Objective
The goal of this international observational study is to learn about the natural history of Danon disease in male patients >8 years of age and female patients
Description
This is an international observational study with both retrospective and prospective data collection. The study is designed to describe the natural history of Danon disease which is a rare x-linked genetic disorder and one of the most severe and penetrant forms of inherited cardiomyopathy. This study will collect data about the clinical course of Danon disease including signs and symptoms, key clinical events, and the impact of the disease on quality of life managed with current standard of care. A hybrid (retrospective and prospective data collection) approach is being taken with the aim of achieving robust and longitudinal data generation.
Subset of patients will be used as an External Control Arm for comparison to RP-A501 Trial participants.
Details
Full study title | An Observational Study of Genetic Cardiomyopathy, Danon Disease |
Protocol number | OCR45634 |
ClinicalTrials.gov ID | NCT06214507 |
Eligibility
Inclusion Criteria:
Prospective Cohort:
Documentation of a pathogenic or likely pathogenic variant of the LAMP2 gene by a CLIA-certified genetic testing laboratory
Patient or parent/legal guardian are capable and willing to provide signed informed consent
Age 鈮� 8 years at enrollment
Female Prospective Cohort:
- Evidence of left ventricular hypertrophy with preserved systolic function in the 12
Months prior to or at enrollment as defined by each of the following:
Retrospective (only) Cohort:
Documentation of a pathogenic or likely pathogenic variant of the LAMP2 gene by a CLIA-certified genetic testing laboratory
Patient or parent/legal guardian are capable and willing to provide signed informed consent, as required by local regulations
Age 鈮� 8 years at enrollment
Prior cardiac transplantation or prior mechanical circulatory support
At least 30 days of retrospective medical records available prior to cardiac transplantation or mechanical circulatory support Female Retrospective (only) Cohort:
Prior evidence of left ventricular hypertrophy.
Exclusion Criteria:
All Cohorts:
Concurrent enrollment in any other clinical investigation involving use of an investigational agent for any condition at time of enrollment to this study that could confound interpretation of this study
Previous treatment with a gene therapy
Prospective Cohort:
Prior mechanical circulatory support at time of enrollment to this study
Prior cardiac transplantation at time of enrollment to this study
Female patients:
- Age >30 years at enrollment
Lead researcher
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Mustafa M Ahmed, MDCardiologist (Heart Specialist), Advanced Heart Failure and Transplant Specialist
Participate in a study
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Step1
Contact the research team
Call or email the research team listed within the specific clinical trial or study to let them know that you're interested. A member of the research team, such as the researcher or study coordinator, will be available to tell you more about the study and to answer any questions or concerns you may have.
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Step2
Get screened to confirm eligibility
You may be asked to take part in prescreening to make sure you are eligible for a study. The prescreening process ensures it is safe for you to participate. During the prescreening process, you will be asked some questions and you may also be asked to schedule tests or procedures to confirm your eligibility.
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Step3
Provide your consent to participate
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Step4
Participate
If you decide to participate in a clinical trial or study, the research team will keep you informed of the study requirements and what you will need to do to throughout the study. For some trials or studies, your health care provider may work with the research team to ensure there are no conflicts with other medications or treatments.