Nilotinib
ApprovedCompleted 0 watching 0 views this week๐ฅ Hot
85
Development Stage
โ
Pre-clinicalโ
Phase 1โ
Phase 2โ
Phase 35
ApprovedIndication / Disease
Philadelphia Chromosome Positive
Conditions
Philadelphia Chromosome Positive, Chronic Myelogenous Leukemia in Chronic Phase
Trial Timeline
Dec 1, 2009 โ 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.
Hype Score Breakdown
Clinical
30
Activity
20
Company
10
Novelty
10
Community
12
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| NCT02774512 | Phase 1 | Withdrawn |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| NCT01270893 | Phase 2 | Withdrawn |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 | 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 |
| 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 | Pfizer | Phase 1/2 | 40 |
| Bosutinib + Bosutinib | Pfizer | Phase 1 | 32 |