A Dose Block-randomized, Double-blind, Placebo-controlled and Dose-escalation Phase I Clinical Trial to Evaluate Safety of BLS-M22 Following Single/Multiple Oral Administration in Healthy Adult Volunteers
Latest Information Update: 04 Nov 2021
At a glance
- Drugs BLS-M22 (Primary)
- Indications Duchenne muscular dystrophy
- Focus Adverse reactions
- Sponsors Bioleaders Corporation
- 21 Apr 2021 Status changed from recruiting to completed.
- 06 Feb 2020 Planned End Date changed from 1 Dec 2019 to 1 Aug 2020.
- 06 Feb 2020 Planned primary completion date changed from 1 Oct 2019 to 1 Jun 2020.