Ly3090106 (DrugBank: -)
1 disease| 告示番号 | 疾患名（ページ内リンク） | 臨床試験数 |
|---|---|---|
| 53 | シェーグレン症候群 | 2 |
| 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 | NCT04563195 (ClinicalTrials.gov) | November 2020 | 12/9/2020 | BAFF/IL-17 Bispecific Antibody Treatment in Subjects With Primary Sjogren's Syndrome | BAFF/IL-17 Bispecific Antibody Treatment in Subjects With Primary Sjogren's Syndrome | Primary Sjogren's Syndrome | Drug: tibulizumab (LY3090106) | Matthew C. Baker | NULL | Not yet recruiting | 18 Years | 85 Years | All | 12 | Phase 2;Phase 3 | United States |
| 2 | NCT02614716 (ClinicalTrials.gov) | December 10, 2015 | 24/11/2015 | A Study of LY3090106 in Participants With Sjögren's Syndrome (SS) | A Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3090106 in Subjects With Sjögren's Syndrome | Sjögren's Syndrome | Drug: LY3090106;Drug: Placebo | Eli Lilly and Company | NULL | Completed | 18 Years | 65 Years | All | 32 | Phase 1 | United States;Bulgaria;Georgia;Romania |