BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + [14C] BMS-813160 + Placebo + BMS-813160 + BMS-813160
Phase 1Completed 0 views this week 0 watching💤 Quiet
Interest: 29/100
29
Development Stage
✓
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Accelerated Intimal Hyperplasia
Conditions
Accelerated Intimal Hyperplasia
Trial Timeline
Feb 1, 2010 → Nov 1, 2010
NCT ID
NCT01049165About BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + [14C] BMS-813160 + Placebo + BMS-813160 + BMS-813160
BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + BMS-813160 + [14C] BMS-813160 + Placebo + BMS-813160 + BMS-813160 is a phase 1 stage product being developed by Bristol Myers Squibb for Accelerated Intimal Hyperplasia. The current trial status is completed. This product is registered under clinical trial identifier NCT01049165. Target conditions include Accelerated Intimal Hyperplasia.
What happened to similar drugs?
0 of 1 similar drugs in Accelerated Intimal Hyperplasia were approved
Approved (0) Terminated (0) Active (1)
Hype Score Breakdown
Clinical
6
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01049165 | Phase 1 | Completed |
Competing Products
4 competing products in Accelerated Intimal Hyperplasia
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Blinatumomab + Cytarabine + Methotrexate + Ponatinib | Amgen | Phase 2 | 42 |
| Pacritinib + Decitabine + Decitabine and Cedazuridine + Azacitidine | Swedish Orphan Biovitrum | Phase 2 | 42 |
| dasatinib + dasatinib | Bristol Myers Squibb | Phase 3 | 40 |
| Ruxolitinib + Enasidenib | Incyte | Phase 2 | 32 |