Letermovir + Placebo
Phase 3Completed 0 views this week 0 watching⚡ Active
Interest: 40/100
40
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Prevention of CMV Infection or Disease
Conditions
Prevention of CMV Infection or Disease
Trial Timeline
Jun 6, 2014 → Nov 21, 2016
NCT ID
NCT02137772About Letermovir + Placebo
Letermovir + Placebo is a phase 3 stage product being developed by Merck for Prevention of CMV Infection or Disease. The current trial status is completed. This product is registered under clinical trial identifier NCT02137772. Target conditions include Prevention of CMV Infection or Disease.
What happened to similar drugs?
9 of 20 similar drugs in Prevention of CMV Infection or Disease were approved
Approved (9) Terminated (0) Active (11)
Hype Score Breakdown
Clinical
17
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (2)
| NCT ID | Phase | Status |
|---|---|---|
| NCT03930615 | Phase 3 | Completed |
| NCT02137772 | Phase 3 | Completed |
Competing Products
20 competing products in Prevention of CMV Infection or Disease
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| mRNA-1944 | Moderna | Phase 1 | 0 |
| Gam-COVID-Vac | Dr. Reddy's Laboratories | Phase 2/3 | 31 |
| edoxaban + enoxaparin sodium | Daiichi Sankyo | Phase 3 | 40 |
| Mifepristone | Eli Lilly | Phase 2 | 35 |
| EXANTA | AstraZeneca | Phase 2 | 27 |
| Risk of low dose aspirin discontinuation | AstraZeneca | Pre-clinical | 26 |
| DAPA/MET XR + DAPA + MET XR | AstraZeneca | Phase 3 | 40 |
| Esomeprazole + Placebo | AstraZeneca | Phase 3 | 40 |
| PCV15 | Merck | Pre-clinical | 18 |
| Raltegravir | Merck | Approved | 43 |
| RotaTeq (V260) + IPV | Merck | Phase 3 | 40 |
| V501 | Merck | Phase 3 | 40 |
| Zostavax | Merck | Phase 3 | 40 |
| V920 Consistency Lot A + V920 Consistency Lot B + V920 Consistency Lot C + V920 High-dose Lot + Placebo to V920 | Merck | Phase 3 | 40 |
| Meningococcal C conjugate vaccine | Novartis | Approved | 43 |
| Enteric-coated mycophenolate sodium | Novartis | Phase 3 | 40 |
| Meningococcal C conjugate vaccine | Novartis | Approved | 43 |
| rMenB+OMV NZ | Novartis | Phase 3 | 40 |
| Enteric-Coated Mycophenolate Sodium | Novartis | Phase 3 | 40 |
| Inclisiran sodium 300 mg (equivalent to 284 mg inclisiran) in 1.5 mL + Placebo in 1.5ml | Novartis | Phase 3 | 44 |