Octavalent HPV with 15 mcg IMX / AAHS + Octavalent HPV with 30 mcg IMX / AAHS + Octavalent HPV with 60 mcg IMX / AAHS + Octavalent HPV with 120 mcg IMX / AAHS + Comparator: Quadrivalent HPV Vaccine (qHPV), (GARDASIL™)

Phase 1Completed
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33
Hype Score

Development Stage

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

Human Papilloma Virus

Conditions

Human Papilloma Virus, Cervical Cancer, Vulvar Cancer, Vaginal Cancer, Genital Warts

Trial Timeline

Apr 1, 2006 → Nov 1, 2009

About Octavalent HPV with 15 mcg IMX / AAHS + Octavalent HPV with 30 mcg IMX / AAHS + Octavalent HPV with 60 mcg IMX / AAHS + Octavalent HPV with 120 mcg IMX / AAHS + Comparator: Quadrivalent HPV Vaccine (qHPV), (GARDASIL™)

Octavalent HPV with 15 mcg IMX / AAHS + Octavalent HPV with 30 mcg IMX / AAHS + Octavalent HPV with 60 mcg IMX / AAHS + Octavalent HPV with 120 mcg IMX / AAHS + Comparator: Quadrivalent HPV Vaccine (qHPV), (GARDASIL™) is a phase 1 stage product being developed by Merck for Human Papilloma Virus. The current trial status is completed. This product is registered under clinical trial identifier NCT00851643. Target conditions include Human Papilloma Virus, Cervical Cancer, Vulvar Cancer.

Hype Score Breakdown

Clinical
10
Activity
5
Company
10
Novelty
3
Community
2

Clinical Trials (1)

NCT IDPhaseStatus
NCT00851643Phase 1Completed