Bosutinib
Phase 1/2Active 0 watching 0 views this week⚡ Active
40
Development Stage
✓
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Philadelphia Chromosome Positive CML
Conditions
Philadelphia Chromosome Positive CML, Accelerated Phase Chronic Myelogenous Leukemia, Blastic Phase Chronic Myelogenous Leukemia, Chronic Phase Chronic Myelogenous Leukemia
Trial Timeline
Jul 6, 2020 → Jul 1, 2028
NCT ID
NCT04258943About Bosutinib
Bosutinib is a phase 1/2 stage product being developed by Pfizer for Philadelphia Chromosome Positive CML. The current trial status is active. This product is registered under clinical trial identifier NCT04258943. Target conditions include Philadelphia Chromosome Positive CML, Accelerated Phase Chronic Myelogenous Leukemia, Blastic Phase Chronic Myelogenous Leukemia.
Hype Score Breakdown
Clinical
13
Activity
8
Company
9
Novelty
4
Community
3
Clinical Trials (13)
| NCT ID | Phase | Status |
|---|---|---|
| NCT05363488 | Pre-clinical | Completed |
| NCT04258943 | Phase 1/2 | Active |
| NCT03128411 | Phase 2 | Completed |
| NCT02906696 | Phase 2 | Terminated |
| NCT02921477 | Phase 1 | UNKNOWN |
| NCT02546375 | Pre-clinical | Completed |
| NCT02501330 | Pre-clinical | Completed |
| NCT02228382 | Approved | Terminated |
| NCT01903733 | Pre-clinical | Completed |
| NCT01331291 | Phase 2 | Completed |
| NCT00759837 | Phase 1 | Completed |
| NCT00725426 | Phase 1 | Completed |
| NCT00261846 | Phase 2 | Completed |
Competing Products
20 competing products in Philadelphia Chromosome Positive CML
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Imatinib Mesylate | Novartis | Phase 2 | 52 |
| Nilotinib | Novartis | Phase 3 | 77 |
| Nilotinib | Novartis | Phase 3 | 77 |
| STI571 400 mg + STI571 600 mg | Novartis | Phase 2 | 52 |
| Induction Phase + Re-Induction Phase + Post-Remission + Maintenance | Novartis | Phase 2 | 52 |
| nilotinib | Novartis | Phase 2 | 52 |
| Asciminib + Nilotinib | Novartis | Phase 3 | 77 |
| imatinib mesylate | Novartis | Phase 2 | 52 |
| Blinatumomab + Asciminib | Novartis | Phase 1/2 | 41 |
| Asciminib | Novartis | Phase 1 | 33 |
| Asciminib Pediatric formulation group + Asciminib Adult formulation group | Novartis | Phase 1/2 | 41 |
| Nilotinib + LDE225 | Novartis | Phase 1 | 33 |
| Nilotinib | Novartis | Approved | 85 |
| Imatinib + Nilotinib + Bosutinib + Dasatinib + Asciminib | Novartis | Phase 3 | 77 |
| Asciminib | Novartis | Approved | 85 |
| Blinatumomab | Amgen | Phase 2 | 51 |
| Treatment with blinatumomab given subcutaneously. | Amgen | Phase 2 | 51 |
| Blinatumomab + Blinatumomab + HyperCVAD | Amgen | Phase 3 | 76 |
| Blinatumomab + Low-intensity chemotherapy regimen + SOC chemotherapy regimen | Amgen | Phase 3 | 76 |
| Bosutinib + Bosutinib | Pfizer | Phase 1 | 32 |