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Trials / Completed

CompletedNCT02667483

Study of DS-5141b in Patients With Duchenne Muscular Dystrophy

Phase I/II Study of DS-5141b: Open-label Study of DS-5141b in Patients With Duchenne Muscular Dystrophy

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Daiichi Sankyo Co., Ltd. · Industry
Sex
Male
Age
5 Years – 10 Years
Healthy volunteers
Not accepted

Summary

This is a phase I/II study to evaluate the safety, tolerability, efficacy, and pharmacokinetic (PK) profile of DS-5141b in patients with Duchenne muscular dystrophy (DMD) amenable to exon 45 skipping and to determine the dosage for subsequent studies.

Conditions

Interventions

TypeNameDescription
DRUGDS-5141bDS-5141b, Subcutaneous injection

Timeline

Start date
2015-10-01
Primary completion
2020-10-20
Completion
2020-10-20
First posted
2016-01-29
Last updated
2024-03-07
Results posted
2024-03-07

Locations

2 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT02667483. Inclusion in this directory is not an endorsement.

Study of DS-5141b in Patients With Duchenne Muscular Dystrophy (NCT02667483) · Clinical Trials Directory