Lenvatinib
Phase 1Completed 1 views this week 0 watching💤 Quiet
Interest: 29/100
29
Development Stage
✓
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Renal Impairment
Conditions
Renal Impairment, Disease Severity
Trial Timeline
Nov 1, 2011 → Oct 1, 2012
NCT ID
NCT02199379About Lenvatinib
Lenvatinib is a phase 1 stage product being developed by Eisai for Renal Impairment. The current trial status is completed. This product is registered under clinical trial identifier NCT02199379. Target conditions include Renal Impairment, Disease Severity.
What happened to similar drugs?
20 of 20 similar drugs in Renal Impairment were approved
Approved (20) Terminated (0) Active (0)
✅Rituximab + Tacrolimus + Mycophenylate mofetil + Hydrocortisone + Prednisolone + PrednisoloneAstellas PharmaApproved
✅Tacrolimus - Prograf® twice daily formulation + Tacrolimus - Advagraf® once daily formulationAstellas PharmaApproved
Hype Score Breakdown
Clinical
6
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT03533361 | Pre-clinical | Completed |
| NCT02211222 | Pre-clinical | Completed |
| NCT05901194 | Phase 1/2 | Active |
| NCT06138769 | Phase 2 | Active |
| NCT05171335 | Phase 2 | Recruiting |
| NCT05103904 | Phase 2 | Recruiting |
| NCT04321954 | Phase 2 | Active |
| NCT04297254 | Approved | Completed |
| NCT04447755 | Phase 2 | Completed |
| NCT04008082 | Pre-clinical | Completed |
| NCT03506048 | Phase 2 | Terminated |
| NCT03009292 | Phase 1 | Completed |
| NCT03663114 | Pre-clinical | Completed |
| NCT02846766 | Phase 2 | Withdrawn |
| NCT03433703 | Phase 2 | Terminated |
| NCT03573960 | Approved | Completed |
| NCT03168074 | Phase 2 | UNKNOWN |
| NCT02953743 | Phase 1 | Completed |
| NCT02780310 | Phase 2 | Active |
| NCT02579616 | Phase 2 | Completed |
Competing Products
20 competing products in Renal Impairment
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| MBX 2109 + MBX 2109 + MBX 2109 + MBX 2109 | MBX Biosciences | Phase 1 | 23 |
| LY3473329 | Eli Lilly | Phase 1 | 29 |
| Tildacerfont/Placebo | Spruce Biosciences | Phase 2 | 17 |
| SPR001 | Spruce Biosciences | Phase 2 | 25 |
| SPR001 | Spruce Biosciences | Phase 2 | 25 |
| Tildacerfont/Placebo | Spruce Biosciences | Phase 2 | 17 |
| Tildacerfont | Spruce Biosciences | Phase 2 | 17 |
| Drotrecogin alfa activated (Xigris) | Eli Lilly | Phase 2 | 35 |
| LY3819469 | Eli Lilly | Phase 1 | 29 |
| Atezolizumab + Cabozantinib | Chugai Pharmaceutical | Phase 3 | 32 |
| DS-6000a + DS-6000a | Daiichi Sankyo | Phase 1 | 33 |
| DS-1093a | Daiichi Sankyo | Phase 1 | 29 |
| CS-3150 | Daiichi Sankyo | Phase 3 | 40 |
| AGS-16C3F | Astellas Pharma | Phase 1 | 29 |
| AGS-16M8F | Astellas Pharma | Phase 1 | 29 |
| CP-461 | Astellas Pharma | Phase 2 | 35 |
| roxadustat | Astellas Pharma | Phase 3 | 40 |
| YM178 | Astellas Pharma | Phase 1 | 29 |
| intravenous immunoglobulins (IVIG) | Astellas Pharma | Phase 1 | 29 |
| bixalomer | Astellas Pharma | Pre-clinical | 26 |