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Quadrivalent human papillomavirus vaccine on-time administration + Quadrivalent human papillomavirus vaccine delayed administration

Pre-clinicalCompleted
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Interest: 26/100
26
Hype Score

Development Stage

1
Pre-clinical
2
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Human Papillomavirus Infection

Conditions

Human Papillomavirus Infection

Trial Timeline

Sep 1, 2007 → Aug 1, 2009

NCT ID
NCT00572832

About Quadrivalent human papillomavirus vaccine on-time administration + Quadrivalent human papillomavirus vaccine delayed administration

Quadrivalent human papillomavirus vaccine on-time administration + Quadrivalent human papillomavirus vaccine delayed administration is a pre-clinical stage product being developed by Merck for Human Papillomavirus Infection. The current trial status is completed. This product is registered under clinical trial identifier NCT00572832. Target conditions include Human Papillomavirus Infection.

What happened to similar drugs?

14 of 20 similar drugs in Human Papillomavirus Infection were approved

Approved (14) Terminated (4) Active (6)
✅lopinavir/ritonavirAbbVieApproved
✅emtricitabine/tenofovir disoproxil fumarateMerckApproved
✅Human Papillomavirus 9-valent Vaccine, RecombinantMerckApproved
✅3-drug anti-HIV therapy + RaltegravirMerckApproved
✅GardasilMerckApproved
✅RaltegravirMerckApproved
✅RaltegravirMerckApproved

Hype Score Breakdown

Clinical
3
Activity
8
Company
15
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT00572832Pre-clinicalCompleted

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