A Phase 1/Phase 2 Open-label Single Arm Study With Dose Escalation (Part A), and Dose Expansion (Part B) Parts to Evaluate the Safety, Tolerability, and Efficacy of SAR446268, an Adeno-associated Viral Vector-mediated Gene Therapy in Participants 10 to 50 Years Old With Non-congenital Myotonic Dystrophy Type 1

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

This is a Phase 1/Phase 2 open-label single arm, multicenter, and multinational study with SAR446268 for treatment of male and female participants 10 to 50 years old with non-congenital myotonic dystrophy (DM) type 1 (DM1). The purpose of this study is to evaluate the safety and efficacy of SAR446268 in knocking down dystrophia myotonica protein kinase (DMPK) messenger ribonucleic acid (mRNA) levels and improving neuromuscular function in DM1 participants receiving a single intravenous (IV) administration of SAR446268. The study consists of a dose escalation part (Part A) during which single ascending doses of SAR446268 will be evaluated in 3 distinct cohorts and an optional 4th dose cohort. Once a safe and effective dose is identified, additional participants will be treated in Part B, the dose expansion phase of the study. The study duration will be 110 weeks (approximately 2 years) for each participant in Parts A and B respectively and includes a 6-week screening phase and a 104-week follow-up period post-SAR446268 administration.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 10
Maximum Age: 50
Healthy Volunteers: f
View:

• For Part A, participants must be 18 to 50 years of age inclusive, at the time of signing the informed consent.

• For Part B, participants must be as follows:

‣ 10 to 17 years of age inclusive, at the time of signing the informed consent or,

⁃ 18 to 50 years of age inclusive, at the time of signing the informed consent.

• Participants with non-congenital onset DM1

• Participants presenting with signs of DM1 including myotonia and muscle weakness, as diagnosed previously by a clinician based on medical history.

• Participants with genetic diagnosis of DM1 \[cytosine-thymine-guanine (CTG) repeat length ≥50 in one allele from medical history\]

• Participants who can walk independently for at least 10 meters at screening (orthoses and ankle braces allowed).

• Participants who have been classified according to cardiac risk by the Investigator as:

‣ Moderate risk participants with pacemaker and/or implantable cardioverter-defibrillator (ICD) for Part A

⁃ Low, moderate, or high cardiac risk for Part B

Locations
United States
Florida
University of Florida Health- Site Number : 8400005
RECRUITING
Gainesville
University of South Florida- Site Number : 8400001
RECRUITING
Tampa
New York
Columbia University Medical Center- Site Number : 8400003
RECRUITING
New York
Other Locations
Argentina
Investigational Site Number : 0320001
RECRUITING
Ciudad Autonoma Buenos Aires
Contact Information
Primary
Trial Transparency email recommended (Toll free for US & Canada)
Contact-US@sanofi.com
800-633-1610
Time Frame
Start Date: 2025-07-23
Estimated Completion Date: 2030-02-28
Participants
Target number of participants: 32
Treatments
Experimental: SAR446268
Participants will receive a single dose of SAR446268 on Day 1
Sponsors
Leads: Sanofi

This content was sourced from clinicaltrials.gov

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