Phase
Condition
Anal Dysplasia
Hiv
Treatment
Human papillomavirus (HPV) vaccine, 9-valent
Clinical Study ID
Ages 18-70 Male Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
18 years old or older and 70 years old or younger
Able to provide informed consent
Denies history of prior HPV vaccination with Gardasil9 (receipt of HPV vaccinationother than Gardasil9 such as the bivalent or the quadrivalent HPV vaccine will beallowed) or unsure of vaccination status and born before 2003
Born Male
For Test group: HIV-positive people born male with current or past exposure to androgen blockers or estrogen (BM-EABE)
Living with HIV
Current or past exposure to androgen blockers or estradiol
For Control group: HIV-negative Control
HIV negative
Either: Current or past exposure to androgen blockers or estradiol; no current orpast exposure to androgen blockers or estradiol AND had sex with a person with apenis in the last year
Exclusion
Exclusion Criteria:
Younger than 18 years old or older than 70 years old.
Self-reported or documented history of nine-valent HPV vaccine or unsure ofvaccination status and born after 2003.
Born female
History of hypersensitivity, including severe reactions to yeast or other componentof the vaccine.
Any condition requiring systemic chemotherapy or immunomodulant affecting antibodyresponses (i.e., rituximab, ibrutinib etc.), intravenous or subcutaneousimmunoglobulin supplementation, radiation therapy, or immunomodulatory treatmentwithin the previous 6 months (presence of precancerous lesions is not exclusionary).
Study Design
Study Description
Connect with a study center
RIIS Clinic at HIPS
Washington, District of Columbia 20002
United StatesSite Not Available
RIIS Clinic at Baltimore Safe Haven
Baltimore, Maryland 21201
United StatesActive - Recruiting
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