Letermovir
Phase 1Recruiting 0 watching 0 views this week💤 Quiet
33
Development Stage
✓
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Cytomegalovirus Prophylaxis
Conditions
Cytomegalovirus Prophylaxis
Trial Timeline
Apr 24, 2026 → May 19, 2028
NCT ID
NCT07199465About Letermovir
Letermovir is a phase 1 stage product being developed by Merck for Cytomegalovirus Prophylaxis. The current trial status is recruiting. This product is registered under clinical trial identifier NCT07199465. Target conditions include Cytomegalovirus Prophylaxis.
Hype Score Breakdown
Clinical
10
Activity
5
Company
10
Novelty
3
Community
2
Clinical Trials (7)
| NCT ID | Phase | Status |
|---|---|---|
| NCT07199465 | Phase 1 | Recruiting |
| NCT06407232 | Phase 3 | Recruiting |
| NCT05789615 | Pre-clinical | Completed |
| NCT05763823 | Phase 3 | Completed |
| NCT04904614 | Approved | Completed |
| NCT04312841 | Phase 2 | Completed |
| NCT03728426 | Phase 2 | Completed |
Competing Products
20 competing products in Cytomegalovirus Prophylaxis
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| ASP0113 + Placebo | Astellas Pharma | Phase 2 | 52 |
| ASP0113 + Placebo | Astellas Pharma | Phase 3 | 77 |
| Letermovir oral granules + Letermovir tablet + Letermovir intravenous | Merck | Phase 2 | 52 |
| Letermovir 240 mg Oral Tablet | Merck | Phase 2 | 52 |
| Letermovir tablet + Letermovir IV | Merck | Phase 3 | 77 |
| Letermovir | Merck | Approved | 85 |
| Letermovir 480 MG [Prevymis] | Merck | Phase 2 | 52 |
| 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 | 33 |
| Ganciclovir | Merck | Pre-clinical | 23 |
| Letermovir + Placebo | Merck | Phase 3 | 77 |
| Letermovir | Merck | Phase 2 | 52 |
| V160 + Placebo | Merck | Phase 2 | 52 |
| V160 | Merck | Phase 1 | 33 |
| Letermovir | Merck | Phase 3 | 77 |
| Letermovir | Merck | Phase 3 | 77 |
| Valganciclovir + Ganciclovir | Roche | Phase 3 | 77 |
| Zidovudine + Didanosine + Ganciclovir | Roche | Phase 1 | 33 |
| Valganciclovir | Roche | Pre-clinical | 23 |
| Foscarnet sodium + Ganciclovir | Roche | Phase 1 | 33 |
| Valganciclovir + Valganciclovir | Roche | Phase 3 | 77 |