nilotinib
Phase 2Completed 0 views this week 0 watching💤 Quiet
Interest: 35/100
35
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Philadelphia Positive (Ph+) Chronic Myelogenous Leukemia
Conditions
Philadelphia Positive (Ph+) Chronic Myelogenous Leukemia
Trial Timeline
Aug 20, 2013 → Aug 28, 2020
NCT ID
NCT01844765About nilotinib
nilotinib is a phase 2 stage product being developed by Novartis for Philadelphia Positive (Ph+) Chronic Myelogenous Leukemia. The current trial status is completed. This product is registered under clinical trial identifier NCT01844765. Target conditions include Philadelphia Positive (Ph+) Chronic Myelogenous Leukemia.
What happened to similar drugs?
2 of 8 similar drugs in Philadelphia Positive (Ph+) Chronic Myelogenous Leukemia were approved
Approved (2) Terminated (1) Active (5)
Hype Score Breakdown
Clinical
12
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| NCT02774512 | Phase 1 | Withdrawn |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| NCT01270893 | Phase 2 | Withdrawn |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 Positive (Ph+) Chronic Myelogenous Leukemia
| 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 |
| 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 |
| Nilotinib | Novartis | Approved | 43 |
| 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 |