U.S., March 29 -- ClinicalTrials.gov registry received information related to the study (NCT06900049) titled 'Evaluation of the Safety, Tolerability, and Efficacy of LE051 in Patients with Duchenne Muscular Dystrophy' on March 23.
Brief Summary: The purpose of this study is to evaluate the safety, tolerability, and efficacy of LE051 intravenous therapy in DMD patients treated with exon 51 skipping therapy.
Study Start Date: Oct. 24, 2024
Study Type: INTERVENTIONAL
Condition:
Duchenne Muscular Dystrophy (DMD)
Intervention:
DRUG: LE051
LE051 dose escalation : dose 1 and dose 2.
Recruitment Status: RECRUITING
Sponsor: Shanghai Jiao Tong University School of Medicine
Information provided by (Responsible Party): Jiwen Wang, Shanghai J...