Rvt-1401 340 mg/weekly (DrugBank: -)
1 disease告示番号 | 疾患名(ページ内リンク) | 臨床試験数 |
---|---|---|
61 | 自己免疫性溶血性貧血 | 1 |
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 | NCT04253236 (ClinicalTrials.gov) | August 11, 2020 | 21/1/2020 | To Assess the Efficacy and Safety of RVT-1401 in the Treatment of Warm Autoimmune Hemolytic Anemia (ASCEND-WAIHA). | A Phase 2, Multicenter, Non-Randomized, Open-Label Study of RVT-1401 for the Treatment of Patients With Warm Autoimmune Hemolytic Anemia | Warm Autoimmune Hemolytic Anemia | Drug: RVT-1401 680 mg/weekly;Drug: RVT-1401 340 mg/weekly | Immunovant Sciences GmbH | NULL | Recruiting | 18 Years | N/A | All | 16 | Phase 2 | United States;Israel;Korea, Republic of;Spain;Thailand;United Kingdom |