13-valent Pneumococcal conjugate vaccine
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84
Development Stage
โ
Pre-clinicalโ
Phase 1โ
Phase 2โ
Phase 35
ApprovedIndication / Disease
Prevention of Pneumonia and Invasive Disease Caused by the Serotypes in 13vPnC
Conditions
Prevention of Pneumonia and Invasive Disease Caused by the Serotypes in 13vPnC
Trial Timeline
Aug 1, 2014 โ Jul 1, 2015
NCT ID
NCT02034877About 13-valent Pneumococcal conjugate vaccine
13-valent Pneumococcal conjugate vaccine is a approved stage product being developed by Pfizer for Prevention of Pneumonia and Invasive Disease Caused by the Serotypes in 13vPnC. The current trial status is completed. This product is registered under clinical trial identifier NCT02034877. Target conditions include Prevention of Pneumonia and Invasive Disease Caused by the Serotypes in 13vPnC.
Hype Score Breakdown
Clinical
30
Activity
20
Company
9
Novelty
10
Community
12
Clinical Trials (10)
| NCT ID | Phase | Status |
|---|---|---|
| NCT05329259 | Approved | Completed |
| NCT03571607 | Phase 3 | Completed |
| NCT02034877 | Approved | Completed |
| NCT01026038 | Phase 3 | Completed |
| NCT00963235 | Phase 3 | Completed |
| NCT00708682 | Phase 3 | Completed |
| NCT00500357 | Phase 3 | Completed |
| NCT00452452 | Phase 3 | Completed |
| NCT00464945 | Phase 3 | Completed |
| NCT00269672 | Phase 2 | Completed |
Competing Products
20 competing products in Prevention of Pneumonia and Invasive Disease Caused by the Serotypes in 13vPnC
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| edoxaban + enoxaparin sodium | Daiichi Sankyo | Phase 3 | 77 |
| Mifepristone | Eli Lilly | Phase 2 | 52 |
| EXANTA | AstraZeneca | Phase 2 | 52 |
| Risk of low dose aspirin discontinuation | AstraZeneca | Pre-clinical | 23 |
| DAPA/MET XR + DAPA + MET XR | AstraZeneca | Phase 3 | 77 |
| Esomeprazole + Placebo | AstraZeneca | Phase 3 | 77 |
| PCV15 | Merck | Pre-clinical | 23 |
| Raltegravir | Merck | Approved | 85 |
| RotaTeq (V260) + IPV | Merck | Phase 3 | 77 |
| V501 | Merck | Phase 3 | 77 |
| Zostavax | Merck | Phase 3 | 77 |
| V920 Consistency Lot A + V920 Consistency Lot B + V920 Consistency Lot C + V920 High-dose Lot + Placebo to V920 | Merck | Phase 3 | 77 |
| Letermovir + Placebo | Merck | Phase 3 | 77 |
| Meningococcal C conjugate vaccine | Novartis | Approved | 85 |
| Enteric-coated mycophenolate sodium | Novartis | Phase 3 | 77 |
| Meningococcal C conjugate vaccine | Novartis | Approved | 85 |
| rMenB+OMV NZ | Novartis | Phase 3 | 77 |
| Enteric-Coated Mycophenolate Sodium | Novartis | Phase 3 | 77 |
| Inclisiran sodium 300 mg (equivalent to 284 mg inclisiran) in 1.5 mL + Placebo in 1.5ml | Novartis | Phase 3 | 77 |
| Meningococcal C Conjugate Vaccine | Novartis | Phase 3 | 77 |