The Natural History of Danon Disease

NCT ID: NCT03766386

Last Updated: 2022-05-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-11-30

Study Completion Date

2024-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Danon disease (DD) is a rare, X-linked disorder associated with severe cardiomyopathy, and in many cases, skeletal myopathy, and cognitive impairment caused by mutations in the LAMP2 gene. There is still uncertainty regarding the natural history of DD because of its rarity.

This study aims to determine the natural history of DD through the collection and analysis of retrospective and prospective data. To achieve this, the investigators will perform surveys and obtain medical records from DD patients. The same cohort of patients will also be assessed by a multidisciplinary team with expertise in DD (cardiologist, neurologist, ophthalmologist, psychologist, geneticist) at the University of California, San Diego. All patients with DD are eligible, including those who underwent a heart transplant. Additionally, data and records from deceased patients will provide valuable retrospective data for this study.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The study design will include:

1. Collection of information for all patients from:

* Survey of patient or caregiver (if the patient has deceased)
* Medical Charts
2. Collection of information from living patients assessed by the multidisciplinary team at the University of California, San Diego including:

* A complete medical history and physical examination
* Cardiac Testing (Electrocardiography; Echocardiography; Cardiac magnetic resonance imaging with gadolinium contrast agent-gadolinium contrast is optional-; Cardiopulmonary Test)
* Pulmonary function testing (PFT)
* Neuromuscular Assessment
* Cognitive Tests
* Vision exam including retinal evaluation
* Laboratory Tests
* Questionnaires on Quality of life
* Needle Skeletal muscle biopsy (only for patients over 18 years old)
* Abdominal Ultrasound for assessment of the liver structure

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Danon Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

OTHER

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Danon Disease Patients

Patients with a confirmed diagnosis of Danon disease who are currently alive (including patients who may or may not have undergone heart transplantation).

No interventions assigned to this group

Deceased Danon Disease Patients

Patients with a confirmed diagnosis of Danon disease who are deceased (including patients who may or may not have undergone heart transplantation).

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

• Living or deceased patients with a diagnosis of Danon disease(including patients who may or may not have undergone heart transplantation) based on a genetic test positive for the LAMP2 mutation

Exclusion Criteria

• Patients without a genetic test positive for a LAMP2 mutation
Minimum Eligible Age

0 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Rocket Pharmaceuticals Inc.

INDUSTRY

Sponsor Role collaborator

University of California, San Diego

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Eric Adler, MD

Professor of Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of California, San Diego

San Diego, California, United States

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

United States

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Eric Adler, MD

Role: CONTACT

8582462996

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Eric Adler, MD

Role: primary

Michela Brambatti, MD,MS

Role: backup

References

Explore related publications, articles, or registry entries linked to this study.

Hong KN, Eshraghian E, Khedro T, Argiro A, Attias J, Storm G, Tsotras M, Bloks T, Jackson I, Ahmad E, Graw S, Mestroni L, Bui QM, Schwartz J, Turner S, Adler ED, Taylor M. An International Longitudinal Natural History Study of Patients With Danon Disease: Unique Cardiac Trajectories Identified Based on Sex and Heart Failure Outcomes. J Am Heart Assoc. 2025 Apr;14(7):e038394. doi: 10.1161/JAHA.124.038394. Epub 2025 Mar 21.

Reference Type DERIVED
PMID: 40118805 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

170727

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

A Natural History of Late Onset Tay-Sachs Disease
NCT02851862 ACTIVE_NOT_RECRUITING
The Prevalence of RYR1-related Disease
NCT06791369 NOT_YET_RECRUITING