HPV Vaccination in HIV Infected and HIV Uninfected Adolescents in Eswatini

Hiv Clinical Trial

Official title:

A Multi-site, Open-label Non-inferiority Trial to Assess Immunogenicity of Two Doses of the Nonavalent Human Papillomavirus (HPV) Vaccine Among Children, Adolescents and Young Adults (9-26 Years) Living With HIV vs Three Doses of Nonavalent HPV Vaccine Among HIV Uninfected Young Women (15-26 Years) in Eswatini

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04982614
• Other study ID #: AAAT6912
• Secondary ID: 7200AA19CA 00003
• Status: Active, not recruiting
• Phase: Phase 4
• Start date: April 1, 2022
• Est. completion date: September 30, 2024

Study information

• Verified date: March 2024
• Source: Columbia University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multi-site, open-label non-inferiority study of the 9vHPV vaccine among a population of children, adolescents and young women living with HIV in Eswatini. This protocol seeks to assess immunogenicity of a two-dose 9vHPV vaccine regimen among girls and boys (9-14 years) and young women (15-26 years) living with HIV on antiretroviral therapy versus a three-dose 9vHPV vaccine regimen among HIV uninfected young women (15-26 years) in Eswatini. The secondary objectives include examining the safety profiles of the two-dose 9vHPV regimen in those living with HIV and the three-dose 9vHPV regimen in HIV-uninfected young women, as well as measuring the completion of the vaccination series among those living with HIV and those who are not infected with HIV.

Description:

Cervical cancer remains a significant threat to public health worldwide and remains the leading cause of cancer-associated mortality in women in Sub Saharan Africa. Cervical cancer-associated morbidity and mortality is preventable through HPV vaccination, and screening and treatment of pre-cancerous lesions. To date, there is no nationwide HPV vaccination program in Eswatini and the country is not eligible for Global Alliance for Vaccines and Immunization (GAVI) procurement of HPV vaccines, and yet the triad of HIV, sexually transmitted infections (STI) and cervical cancer generates a severe disease burden warranting immediate introduction of this intervention. Given the global limitations in vaccine supply and the high cost for procurement, country programs, including in Eswatini, must optimize vaccine resources in order to maximize HPV vaccine coverage.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 1403
• Est. completion date: September 30, 2024
• Est. primary completion date: September 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 9 Years to 26 Years

Eligibility

Inclusion Criteria:

For people living with HIV receiving two-dose regimen:

• Females 9-26 years and males 9-14 years,
• Documented HIV infection,
• Aware of HIV+ status,
• Currently receiving antiretroviral treatment (ART) for HIV infection for at least six months,
• Living in Eswatini,
• For individuals 18+ years: able to provide informed consent,
• For individuals 15-17 years: able to provide informed assent,
• For individuals 9-14 years of age: able to provide informed assent AND accompanied by an adult caregiver who is able to give informed consent,
• Intending to remain in the vicinity of the study sites for the study period

For reference group of HIV-uninfected women receiving three-dose regimen:

• Females 15-26 years,
• Documented negative HIV test at baseline
• Living in Eswatini,
• Able to provide informed assent (15-17 years) or informed consent (18-26 years)
• Intending to remain in the vicinity of the study sites for the study period Exclusion Criteria:

For all participants:

• Diagnosis of other immunosuppressive diseases or receipt of immunosuppressive medications,
• Diagnosis of other acute or chronic illness,
• Receipt of other vaccinations within 2-3 weeks before or after study vaccination,
• Receipt of blood-derived products within 6 months before or during the study,
• Previous receipt of an HPV vaccine,
• Currently pregnant,
• Known allergies to a vaccine component

Related Conditions & MeSH terms

• Hiv
• HPV Infection
• HPV Vaccine
• Papillomavirus Infections

Intervention

Biological:
• Gardasil ® 9
GARDASIL 9 is a vaccine indicated in girls and women 9 through 45 years of age for the prevention of the following diseases: Cervical, vulvar, vaginal, and anal cancer, and Genital warts (condyloma acuminata) caused by Human Papillomavirus (HPV). 0.5-mL suspension for intramuscular injection as a single-dose vial and prefilled syringe at the following regimen/schedule: 9 through 14 years - 2-dose at 0, 6 to 12 months OR 3-dose at 0, 2, 6 months 15 through 45 years - 3-dose at 0, 2, 6 months

Locations

Country	Name	City	State
Swaziland	AHF Lamvelase	Manzini
Swaziland	AHF Manzini	Manzini
Swaziland	Raleigh Fitkin Memorial Hospital	Manzini
Swaziland	AHF Matsapha	Matsapha
Swaziland	Baylor College of Medicine - Bristol Myers-Squibb Children's Clinical Centre of Excellence	Mbabane

Sponsors (3)

Lead Sponsor	Collaborator
Columbia University	Jhpiego, Merck Sharp & Dohme LLC

Country where clinical trial is conducted

Swaziland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Anti-HPV geometric mean antibody titers	Serum antibodies against HPV antigens (IgG, IFNg, TNF, IL2, CXCL10, granzyme, perforin, PTX3). Geometric mean titers will be summarized by treatment group, and the ratios of mean GMTs between treatment and control and their 95% confidence intervals calculated around point estimates.	Month 7 (4 weeks post Month 6 vaccine dose)
Primary	Number of seroconversions	Number of participants who seroconvert, defined as having no HPV antibodies pre-vaccination, but detectable HPV antibodies at 4 weeks post month 6 vaccine dose	Month 7 (4 weeks post Month 6 vaccine dose)
Secondary	Number of participants with serious adverse events (SAE)	Number of participants who reported experiences of SAE. SAE is defined as those that experienced death, life-threatening conditions or hospitalizations.	Up to 6 months
Secondary	Number of participants completing vaccination series	Number of eligible participants completing the 2-dose or 3-dose regimens will be tallied.	Up to 6 months