Letermovir + Placebo
Phase 3Completed 2 views this week 0 watching⚡ Active
Interest: 40/100
40
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Cytomegalovirus Infection
Conditions
Cytomegalovirus Infection
Trial Timeline
Jun 21, 2019 → Mar 16, 2022
NCT ID
NCT03930615About Letermovir + Placebo
Letermovir + Placebo is a phase 3 stage product being developed by Merck for Cytomegalovirus Infection. The current trial status is completed. This product is registered under clinical trial identifier NCT03930615. Target conditions include Cytomegalovirus Infection.
What happened to similar drugs?
7 of 20 similar drugs in Cytomegalovirus Infection were approved
Approved (7) Terminated (3) Active (10)
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 Cytomegalovirus Infection
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| mRNA-1273 | Moderna | Phase 1 | 0 |
| mRNA-1647 | Moderna | Phase 2 | 0 |
| mRNA-1647 | Moderna | Phase 2 | 0 |
| mRNA-1647 | Moderna | Phase 2 | 0 |
| mRNA-1647 | Moderna | Phase 2 | 0 |
| mRNA-1647 | Moderna | Phase 1 | 0 |
| mRNA-1647 | Moderna | Phase 2 | 0 |
| mRNA-1647 | Moderna | Phase 1 | 0 |
| mRNA-1647 | Moderna | Phase 3 | 0 |
| ASP0113 + Placebo | Astellas Pharma | Phase 2 | 35 |
| ASP0113 + Placebo | Astellas Pharma | Phase 3 | 40 |
| Letermovir oral granules + Letermovir tablet + Letermovir intravenous | Merck | Phase 2 | 35 |
| Letermovir 240 mg Oral Tablet | Merck | Phase 2 | 42 |
| Letermovir tablet + Letermovir IV | Merck | Phase 3 | 40 |
| Letermovir | Merck | Phase 1 | 36 |
| Letermovir | Merck | Approved | 43 |
| Letermovir 480 MG [Prevymis] | Merck | Phase 2 | 42 |
| V160 Low Dose IM + V160 Medium Dose IM + V160 High Dose IM + V160 Medium Dose plus Merck Aluminum Phosphate Adjuvant (MAPA) 225 µg /dose IM + V160 High Dose plus MAPA 225 µg /dose IM + V160 Maximum Dose IM + V160 Medium Dose ID | Merck | Phase 1 | 29 |
| Ganciclovir | Merck | Pre-clinical | 26 |
| Letermovir | Merck | Phase 2 | 35 |