BLS-M22 ( DrugBank: BLS-M22 )
1 disease
| ID | Disease name (Link within this page) | Number of trials |
|---|---|---|
| 113 | Muscular dystrophy | 1 |
113. Muscular dystrophy
Clinical trials : 646 / Drugs : 471 - (DrugBank : 105) / Drug target genes : 59 - Drug target pathways : 170
| No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | NCT03789734 (ClinicalTrials.gov) | June 4, 2019 | 12/12/2018 | Safety Study of BLS-M22 in Healthy Volunteers | 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 | Muscular Dystrophy, Duchenne | Biological: BLS-M22;Other: Placebo | BioLeaders Corporation | NULL | Completed | 19 Years | 55 Years | All | 37 | Phase 1 | Korea, Republic of |