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Clinical trial

A Randomized, Double-Blind and Placebo-Controlled Phase I Study to Evaluate the Safety and Primary Immunogenicity of the 9-valent Human Papillomavirus (Types 6, 11, 16, 18,31,33,45,52 and 58) Recombinant Vaccine (Hansenula Polymorpha) in Chinese Female Subjects Aged 9-45 Years

NCT03676101 is registered in ClinicalTrials.gov with Shanghai Bovax Biotechnology Co., Ltd. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Double-Blind and Placebo-Controlled Phase I Study to Evaluate the Safety and Primary Immunogenicity of the 9-valent Human Papillomavirus (Types 6, 11, 16, 18,31,33,45,52 and 58) Recombinant Vaccine (Hansenula Polymorpha) in Chinese Female Subjects Aged 9-45 Years
Lead sponsor
Shanghai Bovax Biotechnology Co., Ltd.
Phase
Phase 1
Overall status
Completed
Start date
October 10, 2018
Completion date
January 10, 2020
Enrollment
90 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

ais, cervical cancers, cin 3, cin1, cin2, genital wart, invasive carcinoma, mild dysplasia of vulva, moderate dysplasia of vulva, vaginal cancer, vain1, vain2, vain3, vin iii, vulvar cancer