BMS-986036
Phase 1Completed 0 watching 0 views this week๐ค Quiet
32
Development Stage
โ
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
NAFLD
Conditions
NAFLD, Nonalcoholic Fatty Liver Disease, Nonalcoholic Steatohepatitis
Trial Timeline
Sep 11, 2018 โ Jun 24, 2019
NCT ID
NCT03674476About BMS-986036
BMS-986036 is a phase 1 stage product being developed by Bristol Myers Squibb for NAFLD. The current trial status is completed. This product is registered under clinical trial identifier NCT03674476. Target conditions include NAFLD, Nonalcoholic Fatty Liver Disease, Nonalcoholic Steatohepatitis.
Hype Score Breakdown
Clinical
10
Activity
5
Company
9
Novelty
3
Community
2
Clinical Trials (8)
| NCT ID | Phase | Status |
|---|---|---|
| NCT04649710 | Phase 1 | Withdrawn |
| NCT04634149 | Phase 1 | Completed |
| NCT04493567 | Phase 1 | Completed |
| NCT03674476 | Phase 1 | Completed |
| NCT03486899 | Phase 2 | Completed |
| NCT03486912 | Phase 2 | Completed |
| NCT03611101 | Pre-clinical | Completed |
| NCT03445208 | Phase 1 | Completed |
Competing Products
15 competing products in NAFLD
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Lanifibranor | Inventiva | Phase 2 | 47 |
| Saroglitazar | Zydus Lifesciences | Approved | 85 |
| AZD4076 + Placebo | AstraZeneca | Phase 1 | 33 |
| AZ compound | AstraZeneca | Phase 2 | 52 |
| Placebo + Omega-3 carboxylic acid + Fenofibrate 200mg + Placebo | AstraZeneca | Phase 2 | 52 |
| LCQ908 + placebo | Novartis | Phase 2 | 52 |
| Placebo + RO5093151 | Roche | Phase 1 | 33 |
| Semaglutide Pen Injector + Placebo | Novo Nordisk | Phase 2 | 51 |
| Ketohexokinase inhibition | Pfizer | Phase 2 | 51 |
| PF-05221304 Monotherapy + PF-06865571 Monotherapy + Placebo + PF-05221304 and PF-06865571 Combination | Pfizer | Phase 2 | 51 |
| ALN-PNP + Placebo | Regeneron Pharmaceuticals | Phase 1 | 32 |
| Legalonยฎ 140 mg | Viatris | Pre-clinical | 20 |
| Elobixibat + Placebo oral tablet | Ipsen | Phase 2 | 49 |
| Placebo + ISIS 703802 40 mg + ISIS 703802 80 mg + ISIS 703802 20 mg | Ionis Pharmaceuticals | Phase 2 | 49 |
| EDP 305 + Placebo | Enanta Pharmaceuticals | Phase 1 | 25 |