DS-2325a ( DrugBank: - )
1 disease
ID | Disease name (Link within this page) | Number of trials |
---|---|---|
160 | Congenital ichthyosis | 2 |
160. Congenital ichthyosis
Clinical trials : 42 / Drugs : 71 - (DrugBank : 21) / Drug target genes : 18 - Drug target pathways : 112
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 | NCT05583669 (ClinicalTrials.gov) | November 8, 2022 | 13/10/2022 | A Study to Assess the Safety and Pharmacokinetics of Multiple Ascending Subcutaneous Doses of DS-2325a in Healthy Subjects | A Phase 1, Subject- and Investigator-Blinded, Sponsor-Unblinded, Placebo-Controlled, Randomized, Sequential Cohort Study to Assess the Safety and Pharmacokinetics of Multiple Ascending Subcutaneous Doses of DS-2325a in Healthy Subjects | Netherton Syndrome | Drug: DS-2325a;Drug: Placebo | Daiichi Sankyo, Inc. | NULL | Recruiting | 18 Years | 50 Years | All | 24 | Phase 1 | United States |
2 | NCT05388903 (ClinicalTrials.gov) | June 20, 2022 | 19/5/2022 | A Study to Assess the Safety and Pharmacokinetics of Single Ascending Subcutaneous and Intravenous Doses of DS-2325a in Healthy Subjects | A Phase 1, Subjects- and Investigator-Blinded, Sponsor-Unblinded, Placebo-Controlled, Randomized, Sequential Cohort Study to Assess the Safety and Pharmacokinetics of Single Ascending Subcutaneous and Intravenous Doses of DS-2325a in Healthy Subjects | Netherton Syndrome | Drug: DS-2325a;Drug: Placebo | Daiichi Sankyo, Inc. | NULL | Completed | 18 Years | 45 Years | All | 64 | Phase 1 | United States |