RATIONALE: Vaccines made from virus proteins may help the body build an effective immune response to prevent cervical cancer. PURPOSE: This pilot study is looking at the side effects of a human papillomavirus vaccine and how well it works in preventing cervical cancer in women in India with HIV-1 infection.
Age range
18 Years – 120 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Safety, in Terms of Grade 3 or 4 Adverse Events Attributed to the Vaccine, According to NCI CTCAE v3.0
Timeframe: 52 weeks from study entry
Number of Patients With Significant Decrease (at the 0.05 Significance Level) in CD4+ Cell Count
Timeframe: Screening/Week 0, Weeks 2, 10, 26, and 52.
Number of Patients With Detectable HPV Antibodies to HPV 16 at Week 28
Timeframe: Week 28
Number of Patients With a Significant Increase in HIV Viral Load
Timeframe: Screening/week 0, weeks, 2, 10, 26 and 52
Number of Patients With Detectable Antibodies to HPV-6
Timeframe: 28 weeks
Number of Patients With Detectable Antibodies to HPV-11
Timeframe: 28 weeks
Number of Patients With Detectable Antibodies to HPV-18
Timeframe: 28 weeks