Prospective Natural History Study of Patients With Myotubular Myopathy and Other CentroNuclear Myopathies (NatHis-CNM)

Institut de Myologie, France

Status

Completed

Conditions

Centronuclear Myopathy

Treatments

Other: Standardized strength, respiratory and motor function assessments

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT03351270

NatHis-CNM

Details and patient eligibility

About

This is the 2 years extension of the prospective and longitudinal study of the natural history and functional status of patients with myotubular myopathy and other centronuclear (CNM) sponsored by Dynacure including ten additional pediatric patients with mutation in MTM1 or DNM2 genes). the patients are planned to be enrolled in one year leading to an expected total number of 70 patients followed at least over 1 year period. Data from the study will be used to characterize the disease course of CNM and determine which outcome measures will be the best to assess the efficacy of potential therapies.

Enrollment

60 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients of any age (newborns included) may participate
Patients over 18 years of age and parent(s)/legal guardian(s) of patients < 18 years of age must be provide written informed consent prior to participating in the study and informed assent will be obtained from minors at least 7 years of age when required by regulation.
Myotubular Centronuclear myopathy (MTMCNM) resulting from a mutation in the MTM1, DNM2 or BIN1 gene
Male or symptomatic female. A symptomatic female will be defined by the motor function assessment by Motor Function Measure (MFM) or North Star Ambulatory Assessment (NSAA) below 80% of the total score.
Willing and able to comply with all protocol requirements and procedures.
In France only: Affiliated to or a beneficiary of a social security category

Exclusion criteria

Other disease which may significantly interfere with the assessment of the MTM CNM and is clearly not related to the disease
Currently enrolled in a treatment study; or treatment with an experimental therapy other than pyridostigmine
For women: pregnancy or current breastfeeding