LAMA2-MD \(Merosin Deficient Congenital Muscular Dystrophy, MDC1A\)
Conditions
Keywords
Early Phase 1, Observational, Natural History, Neuromuscular, Functional Assessments
Brief summary
The goal of this observational study is to understand how young children with LAMA2-related dystrophy move and change over time. We will also learn about how this condition impacts other body systems. Participants will undergo: * Neuromuscular assessments * Blood collections * Swallowing and breathing assessments * Questionnaires
Detailed description
READY CMD LAMA2 is a Pre-Phase 1, single-arm, multicenter, prospective natural history clinical study to evaluate the natural history and potential early outcome measures in subjects with laminin α2-related dystrophy (LAMA2-RD) aged 0-5 years. The study seeks to enroll 44 subjects across 14 sites. NCH will enroll 10 subjects. Subjects will complete in-person visits at Baseline, Month 6, Month 12, Month 18, and Month 24. Within two weeks of the Baseline, Month 12, and Month 24 visits, a remote visit will be performed to repeat and compare remote outcomes with in-person outcomes. Remote visits only will also be performed at Month 3 and Month 9. Adverse events will be captured every three months, beginning at baseline. Phone calls will be made by the coordinator and/or other delegated study staff at months 3, 9, 15, and 21. The total study duration for each subject is up to 24 months. Physical assessments to be performed will depend on the subject's age and may include the following: * Assessment of motor milestones (maintained, lost or acquired) * Neuromuscular Gross Motor Outcome (GRO) * Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP-INTEND) * Motor Function Measure (MFM-20) * Bayley-4 * Respiratory assessments: capnography and collection of data on use of non- invasive ventilation and other respiratory support * Physical exam * Swallow/oromotor assessment: To be performed by physician, occupational therapist, speech language pathologist, or other licensed professional at the site. * Muscle ultrasound may be performed at some sites. Other assessments: * Growth parameters \[head circumference, chest circumference, length, weight, body mass index (BMI)\] * 12-lead electrocardiogram * Mode of feeding * Peds Quality of Life (PedsQL) Neuromuscular Module * Pediatric Evaluation of Disability Inventory (PEDI) * Clinical Global Impression of Change (CGIC), physician and parent/caregiver assessed. * Blood samples will be collected from subjects and stored for biomarker and other research purposes. Blood samples will be collected at each in-person visit. * Data from electronic medical records of evaluations performed as standard of care visits will be collected. Medical history, concomitant medications, and AEs will be collected and assessed for a potential relationship to participation in this study. The total duration of the study for each subject is up to approximately 24 months. A subject will be considered to have competed the study if he/she has completed all assessments up to and including Month 24 assessments. The end of the study is defined as the date of completion of the last scheduled assessment shown in the Schedule of Events for the last subject in the study. Subjects who prematurely discontinue study participation will be encouraged to complete an End-of- Study Visit to include assessment of motor milestones and recording of AEs.
Interventions
None listed
Sponsors
Nationwide Children's Hospital
National Institute of Neurological Disorders and Stroke (NINDS)
Ann & Robert H Lurie Children's Hospital of Chicago
Children's Hospital Medical Center, Cincinnati
University of Iowa
Washington University School of Medicine
Stanford University
University of Utah
University of Rochester
University of Pittsburgh
University of Texas, Southwestern Medical Center at Dallas
University of Minnesota
University of California, Los Angeles
Boston Children's Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
No minimum to 5 Years
Healthy volunteers
No
Inclusion criteria
* Signed informed consent by the subject, parent(s) or legally authorized representative (LAR) and/or assent by the subject (when applicable). * Subject must be aged birth to less than 5.0 years of age at time of consent. * A confirmed diagnosis of LAMA2-RD confirmed via: a: Two pathogenic variants in the LAMA2 gene (via a CLIA-approved laboratory) or: b. muscle biopsy with absence of merosin (laminin-211) and at least one pathogenic variant in the LAMA2 gene * Absence of another confirmed genetic disease. * Willingness to maintain current exercise and/or physical therapy regimen for the duration of the clinical study. * Willingness to comply with the study protocol, including but not limited to, all study procedures and visits.
Exclusion criteria
* Acute medical illness or hospitalization within 30 days prior to informed consent. * Participation in a previous trial of any investigational agent for LAMA2-RD within 1 month prior to informed consent, or use of any other investigational therapy (including off-label use of Losartan) within 30 days prior to informed consent, or participation in other clinical studies, within 30 days (or 3 half-lives, whichever is longer) prior to informed consent, which in the opinion of the PI, may potentially confound results from this study. * Other significant medical condition, which in the opinion of the site Principal Investigator may confound interpretation of the clinical course of LAMA2- RD.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Validate the change over 24 months using the Neuromuscular Gross Motor Outcome | 24 months | The Neuromuscular GRO is a 50-item assessment that measures a child's gross motor function when lying down, sitting, crawling, walking, jumping, and climbing stairs. |
| Validate the change over 24 months using the Bayley Scales of Infant and Toddler Development™ 4th Ed (BayleyTM-4) | 24 months | The Bayley assess four areas of development: Gross Motor, Fine Motor, Speech and Language, and Social. These results are compared to typically developing children ages 15 days to 42 months. The entire assessment takes between 1 and 3 hours, with breaks. |
| Validate the change over 24 months using the Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders | 24 months | The CHOP-Intend includes 16-items to measure a child's ability to move their body in a lying down position, supported sitting, and assisted rolling. |
| Validate the change over 24 months using the Motor Function Measure Scale-Short Form | 24 months | The MFM-20 contains 20 items to assess a child's motor function in sitting, lying down, standing, and completing tabletop activities. |
| Validate the change over 24 months using the World Health Organization motor milestones | 24 months | A child will be asked to complete 6 items to assess attainment of gross motor milestones including sitting without support, crawling, standing, and walking with and without assistance. |
Countries
United States
Contacts
CONTACTKevin Warf
PRINCIPAL_INVESTIGATORAnne M Connolly, MD
Nationwide Childrens Hospital
Outcome results
None listed