Ganciclovir
Pre-clinicalCompleted 0 views this week 0 watching💤 Quiet
Interest: 26/100
26
Development Stage
1
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Cytomegalovirus Infections
Conditions
Cytomegalovirus Infections
Trial Timeline
Sep 15, 2020 → Sep 15, 2022
NCT ID
NCT04478474About Ganciclovir
Ganciclovir is a pre-clinical stage product being developed by Merck for Cytomegalovirus Infections. The current trial status is completed. This product is registered under clinical trial identifier NCT04478474. Target conditions include Cytomegalovirus Infections.
What happened to similar drugs?
6 of 20 similar drugs in Cytomegalovirus Infections were approved
Approved (6) Terminated (3) Active (11)
Hype Score Breakdown
Clinical
3
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT04478474 | Pre-clinical | Completed |
Competing Products
20 competing products in Cytomegalovirus Infections
| 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 |
| Letermovir + Placebo | Merck | Phase 3 | 40 |
| Letermovir | Merck | Phase 2 | 35 |