A multicentre, randomised, double-blind, placebo-controlled and open label extension study to assess the efficacy, safety, and pharmacokinetic profile of two dose levels of ATL1102 administered by subcutaneous injection in non-ambulatory participants with Duchenne Muscular Dystrophy
Latest Information Update: 05 Feb 2025
At a glance
- Drugs ATL 1102 (Primary)
- Indications Duchenne muscular dystrophy
- Focus Adverse reactions; Registrational; Therapeutic Use
- Sponsors Antisense Therapeutics
Most Recent Events
- 30 Jan 2025 According to ClinicalTrials.gov this trial is terminated as the study failed to meet its primary or secondary efficacy endpoints. In consultation with investigators, the sponsor determined that it is not in the best interests of patients for the study to continue.
- 30 Jan 2025 Status changed from active, no longer recruiting to discontinued.
- 28 May 2024 Status changed from recruiting to active, no longer recruiting.