Intralesional HPV Vaccine for Condylomata

Status Recruiting

Clinical Trial Summary

This study will investigate whether injecting genital warts with small quantities of the Gardasil 9 vaccine has an effect on the warts.

Clinical Trial Description

This is a prospective, open-label, proof-of-concept research study to assess the effectiveness of intralesional nonavalent in the treatment of patients with genital condylomata. The study will be conducted at Zuckerberg San Francisco General Hospital. The planned intervention is to provide 10 subjects with at least 3 genital condylomata with intralesional nonavalent human papillomavirus vaccine (Gardasil 9) at 0 and 4 weeks. Then, the study subjects will be followed for a further 8 weeks to monitor for change in wart size and wart number. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05087849
Study type	Interventional
Source	University of California, San Francisco
Contact	Ayan Kusari, MD
Phone	628-206-4777
Email	ayan.kusari@ucsf.edu
Status	Recruiting
Phase	Phase 1/Phase 2
Start date	April 15, 2022
Completion date	July 1, 2024

View Details

See also
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