Ignite Creation Date:
2025-12-25 @ 12:43 AM
Ignite Modification Date:
2026-01-04 @ 12:33 AM
Study NCT ID:
NCT06503367
Status:
RECRUITING
Last Update Posted:
2025-08-12
First Post:
2024-06-21
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Observation Study in Patients Age 0-5 Years With LAMA2-related Congenital Muscular Dystrophy
Sponsor:
Nationwide Children's Hospital
Organization:
Study Overview
Official Title:
Establishing Clinical Trial Readiness for Children 0-5 Years With Congenital Muscular Dystrophy Secondary to LAMA2 Mutations (READY CMD LAMA2)
Status:
RECRUITING
Status Verified Date:
2025-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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
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.
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.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
Secondary ID Infos
| Secondary ID | Type | Domain | Link | View |
|---|---|---|---|---|
| 1U01NS124961-01A1 | NIH | None | https://reporter.nih.gov/quic… | View |