Enzastaurin
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
Cutaneous T-Cell Lymphoma
Conditions
Cutaneous T-Cell Lymphoma
Trial Timeline
Sep 1, 2008 → Feb 1, 2010
NCT ID
NCT00744991About Enzastaurin
Enzastaurin is a phase 2 stage product being developed by Eli Lilly for Cutaneous T-Cell Lymphoma. The current trial status is completed. This product is registered under clinical trial identifier NCT00744991. Target conditions include Cutaneous T-Cell Lymphoma.
What happened to similar drugs?
7 of 20 similar drugs in Cutaneous T-Cell Lymphoma were approved
Approved (7) Terminated (1) Active (12)
Hype Score Breakdown
Clinical
12
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (11)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01432951 | Phase 1 | Completed |
| NCT00744991 | Phase 2 | Completed |
| NCT00718419 | Phase 2 | Completed |
| NCT00542919 | Phase 2 | Completed |
| NCT00475644 | Phase 2 | Completed |
| NCT00452257 | Phase 1 | Completed |
| NCT00420381 | Phase 2 | Completed |
| NCT00428714 | Phase 2 | Completed |
| NCT00309140 | Phase 2 | Completed |
| NCT00088205 | Phase 2 | Completed |
| NCT00190723 | Phase 2 | Completed |
Competing Products
20 competing products in Cutaneous T-Cell Lymphoma
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| ONTAK (denileukin difitox, DAB389IL-2) | Eisai | Approved | 43 |
| ONTAK | Eisai | Approved | 43 |
| E7777 9 mcg/kg | Eisai | Phase 3 | 40 |
| ONTAK | Eisai | Approved | 43 |
| Mogamulizumab | Kyowa Kirin | Approved | 47 |
| Mogamulizumab + Brentuximab vedotin | Kyowa Kirin | Phase 1 | 36 |
| Mogamulizumab | Kyowa Kirin | Phase 2 | 39 |
| KW-0761 + Vorinostat | Kyowa Kirin | Phase 3 | 40 |
| Clopidogrel + Ticagrelor | AstraZeneca | Approved | 43 |
| Pembrolizumab | Merck | Phase 2 | 42 |
| Comparator: vorinostat | Merck | Pre-clinical | 26 |
| Pembrolizumab | Merck | Phase 2 | 39 |
| TR701 FA | Merck | Phase 2 | 35 |
| MK0683, vorinostat, Suberoylanilide Hydroxamic Acid (SAHA) / Duration of Treatment 6 Months | Merck | Phase 2 | 35 |
| Pembrolizumab | Merck | Phase 2 | 42 |
| Tulisokibart + Placebo | Merck | Phase 2 | 39 |
| Aspirin + Ipilimumab + Pembrolizumab | Merck | Phase 2 | 35 |
| Pembrolizumab + Mogamulizumab | Merck | Phase 2 | 42 |
| TR-701 FA + Linezolid | Merck | Phase 3 | 40 |
| Pimasertib + Dacarbazine | Merck | Phase 2 | 35 |