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Study of ASP2957 in Male Participants With X-linked Myotubular Myopathy Who Need Ventilators

StatusRecruiting
PhasePhase 1/2
Started
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Record History

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  1. Minor Re-verified, no change to tracked fieldsv10
  2. Minor Study sites: 4 to 5v9
  3. Minor 2 versions Re-verified since May 27, 2026, no change to tracked fieldsv7-v8
  4. Minor Study sites: 3 to 4v6
  5. Minor Study sites: 2 to 3
    • Eligibility criteria expanded, about 4 words
    v5
Show 3 earlier versionsHide 3 earlier versions
  1. Notable Start date: Sep 11, 2025 to Dec 15, 2025
    • Study sites: 1 to 2
    v4
  2. Notable Trial status: Not Yet Recruiting to Recruitingv3 Show 5 more changesShow less
    • Study sites: 0 to 1
    • Primary and study completion dates: Aug 31, 2027 to Oct 31, 2027
    • Start date changed from estimate of Sep 30, 2025 to Sep 11, 2025
    • Eligibility criteria expanded, about 58 words
    • Study title revised
  3. Notable Start date: Jul 31, 2025 to Sep 30, 2025
    • Primary endpoints: 7 to 8
    • Eligibility criteria expanded, about 23 words
    • Secondary endpoints revised (9)
    v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
X-linked myotubular myopathy (XLMTM) is a rare and serious condition present at birth where the muscles do not work properly. There are currently no approved therapies for XLMTM. The protein myotubularin is needed for muscle development, movement and breathing. A gene called MTM1 tells the body to make myotubularin. XLMTM is caused by changes, or mutations, in the MTM1 gene. Changes in the MTM1 gene cause low or no levels of myotubularin to be made, so the muscles do not work properly. Gene therapy is a way of getting a healthy copy of a gene into the body. This allows the body's cells to make a normal protein that may reduce disease symptoms. Researchers have developed ASP2957 to get a healthy MTM1 gene into the body. This could help improve muscle development and function in young children with XLMTM. In this study, ASP2957 will be given to humans for the first time. ASP2957 has the healthy MTM1 gene inside a type of empty (killed) virus. The virus delivers the healthy MTM1 gene directly into cells in the body. It's possible that some boys may have antibodies to the virus if they have previously been infected with a similar virus. The antibodies could stop ASP2957 from working properly and cause an immune reaction to ASP2957. To prevent this, the boys will also be given medicines to lower the immune system. The main aims of this study are to check the safety of ASP2957, how well it is tolerated, and to find a suitable dose of ASP2957. The study was designed in 2 phases. In Phase 1, different small groups of boys will receive lower to higher doses of ASP2957. Each boy will receive a single infusion of ASP2957. Any medical problems will be recorded for each dose. This is done to find a suitable dose of ASP2957 to use in Phase 2. In Phase 2, another small group of young boys will receive a single infusion of ASP2957. The most suitable dose of ASP2957 worked out from Phase 1 will be used. The boys will be checked for up to 1 year after their single infusion of ASP2957. After this, there will be the option for the boys to join another study so they will continue to be checked longer term.
Trial Details
NCT Number NCT07052929
Lead Sponsor Astellas Gene Therapies
Conditions
(from sponsor)
X-Linked Myotubular Myopathy
Related terms Myopathies, Structural, Congenital
Enrollment 9 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov