mRNA-1647
Phase 2Withdrawn 1 views this week 0 watching
0
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Cytomegalovirus Infection
Conditions
Cytomegalovirus Infection
Trial Timeline
Feb 8, 2024 → Feb 14, 2027
NCT ID
NCT06133010About mRNA-1647
mRNA-1647 is a phase 2 stage product being developed by Moderna for Cytomegalovirus Infection. The current trial status is withdrawn. This product is registered under clinical trial identifier NCT06133010. Target conditions include Cytomegalovirus Infection.
What happened to similar drugs?
8 of 20 similar drugs in Cytomegalovirus Infection were approved
Approved (8) Terminated (1) Active (11)
Clinical Trials (8)
| NCT ID | Phase | Status |
|---|---|---|
| NCT06133010 | Phase 2 | Withdrawn |
| NCT05683457 | Phase 2 | Recruiting |
| NCT05575492 | Phase 2 | Active |
| NCT05105048 | Phase 1 | Completed |
| NCT05085366 | Phase 3 | Terminated |
| NCT04975893 | Phase 2 | Completed |
| NCT04232280 | Phase 2 | Completed |
| NCT03382405 | Phase 1 | 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 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 + Placebo | Merck | Phase 3 | 40 |
| Letermovir | Merck | Phase 2 | 35 |