V920 Consistency Lot A + V920 Consistency Lot B + V920 Consistency Lot C + V920 High-dose Lot + Placebo to V920
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 Ebola Infection
Conditions
Prevention of Ebola Infection
Trial Timeline
Aug 17, 2015 → Sep 29, 2017
NCT ID
NCT02503202About V920 Consistency Lot A + V920 Consistency Lot B + V920 Consistency Lot C + V920 High-dose Lot + Placebo to V920
V920 Consistency Lot A + V920 Consistency Lot B + V920 Consistency Lot C + V920 High-dose Lot + Placebo to V920 is a phase 3 stage product being developed by Merck for Prevention of Ebola Infection. The current trial status is completed. This product is registered under clinical trial identifier NCT02503202. Target conditions include Prevention of Ebola Infection.
What happened to similar drugs?
9 of 20 similar drugs in Prevention of Ebola Infection were approved
Approved (9) Terminated (0) Active (11)
Hype Score Breakdown
Clinical
17
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT02503202 | Phase 3 | Completed |
Competing Products
20 competing products in Prevention of Ebola Infection
| 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 |
| Letermovir + Placebo | 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 |