BMS-986165
ApprovedRecruiting 0 views this week 0 watching⚡ Active
Interest: 50/100
50
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Systemic Lupus Erythematosus (SLE)
Conditions
Systemic Lupus Erythematosus (SLE), Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE)
Trial Timeline
Feb 27, 2026 → Dec 1, 2026
NCT ID
NCT06875960About BMS-986165
BMS-986165 is a approved stage product being developed by Bristol Myers Squibb for Systemic Lupus Erythematosus (SLE). The current trial status is recruiting. This product is registered under clinical trial identifier NCT06875960. Target conditions include Systemic Lupus Erythematosus (SLE), Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE).
What happened to similar drugs?
9 of 20 similar drugs in Systemic Lupus Erythematosus (SLE) were approved
Approved (9) Terminated (4) Active (8)
Hype Score Breakdown
Clinical
20
Activity
15
Company
15
Novelty
0
Community
0
Clinical Trials (14)
| NCT ID | Phase | Status |
|---|---|---|
| NCT06875960 | Approved | Recruiting |
| NCT04613518 | Phase 2 | Completed |
| NCT04167462 | Phase 3 | Completed |
| NCT03934216 | Phase 2 | Completed |
| NCT03924427 | Phase 3 | Completed |
| NCT03890770 | Phase 1 | Completed |
| NCT03956953 | Phase 1 | Completed |
| NCT03920267 | Phase 2 | Completed |
| NCT03890809 | Phase 1 | Completed |
| NCT03873415 | Phase 1 | Completed |
| NCT03739788 | Phase 1 | Completed |
| NCT03599622 | Phase 2 | Terminated |
| NCT03252587 | Phase 2 | Completed |
| NCT03004768 | Phase 1 | Completed |
Competing Products
20 competing products in Systemic Lupus Erythematosus (SLE)
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Tabalumab Auto-Injector + Tabalumab Prefilled Syringe | Eli Lilly | Phase 3 | 32 |
| Baricitinib + Placebo | Eli Lilly | Phase 2 | 35 |
| MRA(Tocilizumab) + placebo | Chugai Pharmaceutical | Phase 3 | 40 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 40 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 40 |
| DS-7011a + Placebo | Daiichi Sankyo | Phase 1 | 29 |
| DS-7011a + Placebo | Daiichi Sankyo | Phase 1/2 | 32 |
| Bocidelpar + Placebo | Astellas Pharma | Phase 1 | 21 |
| Parenteral micafungin application + Other parenteral antifungal drugs | Astellas Pharma | Pre-clinical | 26 |
| Micafungin | Astellas Pharma | Phase 2 | 35 |
| E6742 | Eisai | Phase 1/2 | 32 |
| KHK4827 | Kyowa Kirin | Phase 1 | 29 |
| KHK4827 + Placebo | Kyowa Kirin | Phase 3 | 40 |
| Baricitinib + Placebo | Eli Lilly | Phase 3 | 40 |
| Baricitinib + Cyclophosphamide | Eli Lilly | Approved | 47 |
| Baricitinib + Placebo | Eli Lilly | Phase 3 | 32 |
| LY2127399 + Placebo every 2 weeks + Placebo every 4 weeks + Standard of Care | Eli Lilly | Phase 3 | 40 |
| LY3361237 + Placebo | Eli Lilly | Phase 2 | 27 |
| LY2127399 + Placebo | Eli Lilly | Phase 3 | 32 |
| LY3361237 + Placebo | Eli Lilly | Phase 1 | 29 |