A Clinical Trial to Evaluate the Immunogenicity of the Nonavalent Vaccine Against Human Papillomavirus in Men Infected by HIV Who Have Sex With Men. GESIDA 10017
Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Fundacion SEIMC-GESIDA
With
Merck Sharp & Dohme LLC
The investigators estimate that 166 participants will need to be included in the study to evaluate the immunogenicity of vaccine against human papillomavirus in men with HIV infection who have sex with men, by evaluating in two age groups and the seroconversion rate for each of the HPV genotypes included in the vaccine from baseline to month 7 and 24.
Age
18–36
Sex
MALE
Healthy volunteers
Not accepted
You may be eligible if
Patients able to give their written consent to participate in the study. (preferably in writing or, failing that, orally before independent witnesses of the research team) after having received information about the design, the purposes of the study, the possible risks that may arise from it and the possibility of withdrawing from it at any time. moment.
Understand the purpose of the study and be available to perform the visits stipulated in the protocol.
Be ≥18 years and \<of 36 years.
Patient with chronic infection with HIV-1.
Viral HIV load \<50 copies / ml and CD4\> 200 cells / uL for at least the last six months.
Transgender men or women who have had insertive or receptive anal sex with other men
You may not be if
Previous history of anal cancer.
Have previously received any vaccine against HPV.
Clareo Health | A Clinical Trial to Evaluate the Immunogenicity of the Nonavalent Vaccine Against Human Papillomavirus in Men Infected by HIV Who Have Sex With Men. GESIDA 10017
