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Nemaline Myopathy Clinical Research Network (NM-CTRN)

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Stanford University

Status

Not yet enrolling

Conditions

Nemaline Myopathy

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this study is to establish a research network to help define the natural disease history and clinical outcome measures for Nemaline Myopathy (NM).

Full description

The long-term aim of this study is to incorporate these outcome measures into clinical trials for NM therapies. Outcome measures to be assessed will be dependent on the participant's age and functional status. Follow-up visits will be conducted either every 3 or 6 months, dependent on age, for a total of 3 years.

Enrollment

50 estimated patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 0-18 years of age at recruitment
  • Confirmation of Nemaline Myopathy (pathogenic or likely pathogenic mutations in ACTA1 (AD) or NEB (AR)
  • Patient and/or parent or legal guardian must be willing and able to provide informed consent

Exclusion criteria

  • Clinically significant medical finding on the physical examination, other than NM, that the Investigator deems unsuitable for participation in and/or completion of the study procedures
  • Any confirmed chronic or acute condition or disease affecting any system(s), which could interfere with the results of the study and/or the compliance with the study procedures. This will be subject to the clinical judgement of the Principal Investigator (PI)
  • Participants of ongoing (interventional) clinical trials that assess the efficacy of potential treatments will be excluded
  • Safety concerns

Trial design

50 participants in 1 patient group

Individuals with Nemaline Myopathy
Description:
All participants in the study will have a diagnosis of Nemaline Myopathy, with either a pathogenic or likely pathogenic mutation in ACTA1 (AD) or NEB (AR). Participants can be either ambulatory or non-ambulatory and must be between the ages of 0-18.

Trial contacts and locations

6

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Central trial contact

Sarah Ismail, BSc; Carolina Tesi-Rocha, MD

Data sourced from clinicaltrials.gov

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