Nilotinib
Phase 3Completed 0 watching 0 views this week๐ Rising
77
Development Stage
โ
Pre-clinicalโ
Phase 1โ
Phase 24
Phase 35
ApprovedIndication / Disease
Philadelphia Chromosome Positive (PH+) Chronic Myelogenous Leukemia in Chronic Phase (CML-CP)
Conditions
Philadelphia Chromosome Positive (PH+) Chronic Myelogenous Leukemia in Chronic Phase (CML-CP)
Trial Timeline
Apr 15, 2013 โ Jul 8, 2020
NCT ID
NCT01743989About Nilotinib
Nilotinib is a phase 3 stage product being developed by Novartis for Philadelphia Chromosome Positive (PH+) Chronic Myelogenous Leukemia in Chronic Phase (CML-CP). The current trial status is completed. This product is registered under clinical trial identifier NCT01743989. Target conditions include Philadelphia Chromosome Positive (PH+) Chronic Myelogenous Leukemia in Chronic Phase (CML-CP).
Hype Score Breakdown
Clinical
27
Activity
18
Company
10
Novelty
9
Community
10
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| NCT02774512 | Phase 1 | Withdrawn |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| NCT01270893 | Phase 2 | Withdrawn |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 (PH+) Chronic Myelogenous Leukemia in Chronic Phase (CML-CP)
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Imatinib Mesylate | Novartis | Phase 2 | 52 |
| 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 | Pfizer | Phase 1/2 | 40 |
| Bosutinib + Bosutinib | Pfizer | Phase 1 | 32 |