findmyKOL
Clinical trialNCT06281119Active, not recruitingPhase 3Interventional

Clinical Study to Evaluate SIIPL qHPV Vaccine (CERVAVAC®) in Women Living With HIV Aged 15-25 Years

SponsorSerum Institute of India Pvt. Ltd.Enrollment450Human Papillomavirus Infection
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Human papillomavirus (HPV) infection is the most common viral infection of the reproductive tract. Up to 80%of the sexually active females and men will be infected with HPV at some point in their lives and some may be repeatedly infected. The main burden of HPV-related disease is due to cervical cancer. Since cervical screening only detects precancerous and cancerous changes after they have occurred, HPV vaccination is primary prevention. People with HIV infection, even when effectively treated with antiretroviral therapy (ARV),are at higher risk of acquiring infection with multiple HPV types and are also known to be predisposed to a higher risk of HPV infection and subsequent CIN lesions. Vaccination of this high-risk group with HPV vaccine is highly beneficial. SIIPL's qHPV vaccine CERVAVAC®, India's first indigenous qHPV vaccine has received marketing authorization in India. The current study is a Phase 3b study to evaluate the immunogenicity and safety of two- and three-dose schedules of SIIPL qHPV vaccine in women living with HIV (WLWH) aged 15-25years.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Carla Chibwesha

    Clinical HIV Research Unit, Helen Joseph Hospital, Johannesburg, South Africa

    Principal Investigator
  • Nelly Mugo

    CCR, KEMRI, Nairobi-Kenya & PHRD, Thika-Kenya

    Principal Investigator
  • Tacilta Nhampossa

    Manhiça Health Research Center - Manhiça Foundation,Manhiça

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Kenya
  • Centre for Clinical Research, Kemri

    Nairobi, Kenya

  • Partners in Health and Research Development (phrd)

    Thika, Kenya

Mozambique
  • Manhiça Health Research Center - Manhiça Foundation (cism-Fm)

    Manhiça, Mozambique

South Africa
  • Clinical Hiv Research Unit (chru), Helen Joseph Hospital

    Johannesburg, South Africa

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Cervavac as three dose regimenCervavac as two dose regimenGardasil as three dose regimen
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
3 Oct 2025
Primary completion
31 Dec 2026
Completion
31 Dec 2027
Last update posted
29 Jun 2026
Registered enrollment
450
Registry id
NCT06281119

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.