A Phase 1/2/3 Open-label Study to Evaluate the Safety, Tolerability, Efficacy, Pharmacodynamics, and Pharmacokinetics of Intravenous RGX-202 Gene Therapy in Males With Duchenne Muscular Dystrophy (DMD)

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Genetic
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

RGX-202 is a gene therapy designed to deliver a transgene for a novel microdystrophin that includes functional elements of naturally-occurring dystrophin including the C-Terminal (CT) domain. This is a multicenter, open-label dose evaluation clinical study to assess the safety, tolerability, and clinical efficacy of a one-time intravenous (IV) dose of RGX-202 in participants with Duchenne.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 1
Healthy Volunteers: f
View:

• The participant's legal guardian(s) is (are) willing and able to provide written, signed informed consent prior to any study-related procedures; and, where applicable, the minor participant has provided written or verbal assent according to local requirements.

• Is a male at least 4 years of age and less than 12 years of age at consent or 1 to \<4 years of age at the time of dosing and ≥ 10 kg at the time of screening.

• Must meet any of the following criteria:

‣ DMD gene mutation in exons 18 and above, and a clinical picture consistent with typical DMD with the exception of a participant (Cohort 1b) with DMD gene mutation in exons 12-17.

⁃ Participant is able to walk 100 meters independently without assistive devices. Cohort 2c participant must be able to walk 10 meters independently without assistive devices. Cohort 1b participant must be able to walk with or without assistive devices.

⁃ Participant is able to complete the TTSTAND per protocol-specific criteria.

⁃ Participant has been on a stable dose of systemic glucocorticoids according to the standard of care for at least 12 weeks. Cohort 2c participants must be consistently on or off a stable dose of systemic glucocorticoids according to the standard of care for at least 12 weeks.

⁃ Clinical laboratory test results, including hepatic and renal function, are within the normal range during screening, or if abnormal, are not clinically significant, in the opinion of the investigator.

⁃ Documentation is provided at screening visit for participant's adherence to the local country's vaccination schedule. The parent(s) or legal guardian(s) must be willing to have their child receive a meningococcal vaccine, if not already vaccinated.

⁃ Participant and parent(s)/legal guardian(s) are willing and able to comply with scheduled visits, study intervention administration plan, and study procedures.

• The participant's legal guardian(s) is (are) willing and able to provide written, signed informed consent prior to any study-related procedures; and, where applicable, the minor participant has provided written or verbal assent according to local requirements.

• DMD gene mutation with any mutation except for those with deletions or point mutations in exons 8, 9 and/or 10.

• Participant is able to complete the TTSTAND per protocol-specific criteria.

• Clinical laboratory test results, including hepatic and renal function, are within the normal range during screening, or if abnormal, are not clinically significant, in the opinion of the investigator.

• Documentation is provided at screening visit for participant's adherence to the local country's vaccination schedule. The parent(s) or legal guardian(s) must be willing to have their child receive a meningococcal vaccine, if not already vaccinated.

• Participant and parent(s)/legal guardian(s) are willing and able to comply with scheduled visits, study intervention administration plan, and study procedures.

• Is a male at least 1 year of age and ≥ 10 kg at the time of screening.

• Participants 1 to \<4 years of age must meet the following criteria:

‣ is able to walk 10 meters independently without assistive devices.

⁃ must be consistently on or off a stable dose of systemic glucocorticoids according to the standard of care for at least 12 weeks.

• Participants 4 years and older must meet the following criteria:

‣ are able to walk 100 meters independently without assistive devices.

⁃ have been on a stable dose of systemic glucocorticoids according to the standard of care for at least 12 weeks.

⁃ have a NSAA total score ≥16.

Locations
United States
Arkansas
Arkansas Children's Hospital
RECRUITING
Little Rock
California
Stanford School of Medicine /Division of Neuromuscular Medicine
RECRUITING
Palo Alto
Colorado
Children's Hospital Colorado
RECRUITING
Aurora
Illinois
Ann & Robert H. Lurie Children's Hospital of Chicago
RECRUITING
Chicago
Texas
The University of Texas Southwestern Medical Center
RECRUITING
Dallas
Virginia
Children's Hospital of Richmond at Virginia Commonwealth University
RECRUITING
Richmond
Other Locations
Canada
Children's Hospital London Health Science Centre
NOT_YET_RECRUITING
London
Contact Information
Primary
Patient Advocacy
Duchenne@regenxbio.com
(833) 711-0349
Time Frame
Start Date: 2023-01-04
Estimated Completion Date: 2028-08
Participants
Target number of participants: 65
Treatments
Experimental: Part 1: Cohort 1 and 1b: RGX-202 Dose 1
A single IV infusion of RGX-202 at a dose of 1×10\^14 GC/kg body weight
Experimental: Part 1: Cohort 2, 2c;, and Part 2; and Part 3: RGX-202 Dose 2
A single IV infusion of RGX-202 at a dose of 2x10\^14 GC/kg body weight
Sponsors
Leads: REGENXBIO Inc.

This content was sourced from clinicaltrials.gov