Nilotinib
ApprovedCompleted 0 views this week 0 watching⚡ Active
Interest: 43/100
43
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Philadelphia Chromosome Positive
Conditions
Philadelphia Chromosome Positive, Chronic Myelogenous Leukemia in Chronic Phase
Trial Timeline
Dec 1, 2009 → Jan 1, 2014
NCT ID
NCT01043874About Nilotinib
Nilotinib is a approved stage product being developed by Novartis for Philadelphia Chromosome Positive. The current trial status is completed. This product is registered under clinical trial identifier NCT01043874. Target conditions include Philadelphia Chromosome Positive, Chronic Myelogenous Leukemia in Chronic Phase.
What happened to similar drugs?
1 of 7 similar drugs in Philadelphia Chromosome Positive were approved
Approved (1) Terminated (1) Active (5)
Hype Score Breakdown
Clinical
20
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT04559555 | Pre-clinical | Completed |
| NCT04498871 | Pre-clinical | Completed |
| NCT04518644 | Pre-clinical | Completed |
| NCT02774512 | Phase 1 | Withdrawn |
| NCT02546674 | Approved | Completed |
| NCT02115386 | Phase 3 | Terminated |
| NCT02353728 | Phase 2 | Completed |
| NCT02108951 | Phase 3 | Terminated |
| NCT01844765 | Phase 2 | Completed |
| NCT01744665 | Phase 2 | Completed |
| NCT01863745 | Phase 2 | Completed |
| NCT03332511 | Approved | Completed |
| NCT01743989 | Phase 3 | Completed |
| NCT01735955 | Approved | Completed |
| NCT01698905 | Phase 2 | Completed |
| NCT01562847 | Pre-clinical | UNKNOWN |
| NCT01077544 | Phase 1 | Completed |
| NCT01254188 | Phase 3 | Completed |
| NCT01274351 | Phase 2 | Completed |
| NCT01270893 | Phase 2 | Withdrawn |
Competing Products
20 competing products in Philadelphia Chromosome Positive
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Imatinib Mesylate | Novartis | Phase 2 | 35 |
| Nilotinib | Novartis | Phase 3 | 32 |
| Nilotinib | Novartis | Phase 3 | 40 |
| STI571 400 mg + STI571 600 mg | Novartis | Phase 2 | 35 |
| Induction Phase + Re-Induction Phase + Post-Remission + Maintenance | Novartis | Phase 2 | 42 |
| nilotinib | Novartis | Phase 2 | 35 |
| Asciminib + Nilotinib | Novartis | Phase 3 | 44 |
| imatinib mesylate | Novartis | Phase 2 | 35 |
| Blinatumomab + Asciminib | Novartis | Phase 1/2 | 39 |
| Asciminib | Novartis | Phase 1 | 36 |
| Asciminib Pediatric formulation group + Asciminib Adult formulation group | Novartis | Phase 1/2 | 39 |
| Nilotinib + LDE225 | Novartis | Phase 1 | 29 |
| Imatinib + Nilotinib + Bosutinib + Dasatinib + Asciminib | Novartis | Phase 3 | 44 |
| Asciminib | Novartis | Approved | 47 |
| Blinatumomab | Amgen | Phase 2 | 35 |
| Treatment with blinatumomab given subcutaneously. | Amgen | Phase 2 | 42 |
| Blinatumomab + Blinatumomab + HyperCVAD | Amgen | Phase 3 | 47 |
| Blinatumomab + Low-intensity chemotherapy regimen + SOC chemotherapy regimen | Amgen | Phase 3 | 47 |
| Bosutinib | Pfizer | Phase 1/2 | 36 |
| Bosutinib + Bosutinib | Pfizer | Phase 1 | 29 |