Imatinib Mesylate
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 Chromosome Positive Acute Lymphocytic Leukemia
Conditions
Philadelphia Chromosome Positive Acute Lymphocytic Leukemia
Trial Timeline
Oct 1, 2003 → Feb 1, 2007
NCT ID
NCT00154349About Imatinib Mesylate
Imatinib Mesylate is a phase 2 stage product being developed by Novartis for Philadelphia Chromosome Positive Acute Lymphocytic Leukemia. The current trial status is completed. This product is registered under clinical trial identifier NCT00154349. Target conditions include Philadelphia Chromosome Positive Acute Lymphocytic Leukemia.
What happened to similar drugs?
2 of 8 similar drugs in Philadelphia Chromosome Positive Acute Lymphocytic 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 |
|---|---|---|
| NCT01742299 | Approved | Active |
| NCT00867113 | Phase 2 | Completed |
| NCT00732784 | Phase 1 | Completed |
| NCT01172548 | Phase 2 | Completed |
| NCT01483014 | Phase 2 | Completed |
| NCT00684411 | Phase 2 | Completed |
| NCT01545427 | Phase 2 | Terminated |
| NCT00479934 | Phase 2 | Completed |
| NCT00677092 | Phase 2 | Completed |
| NCT00555581 | Phase 2 | Completed |
| NCT00510354 | Approved | Completed |
| NCT00427583 | Phase 2/3 | Terminated |
| NCT00124748 | Phase 3 | Terminated |
| NCT00171899 | Approved | Completed |
| NCT00171912 | Phase 2 | Completed |
| NCT00171977 | Approved | Completed |
| NCT00171938 | Phase 2 | Terminated |
| NCT00154349 | Phase 2 | Completed |
| NCT00237172 | Phase 2 | Completed |
| NCT00171860 | Phase 2 | Terminated |
Competing Products
20 competing products in Philadelphia Chromosome Positive Acute Lymphocytic Leukemia
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| 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 |
| 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 |