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Multi-Center, Randomized, Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern
The study will evaluate the clinical efficacy of different dosing regimens of the Moderna COVID-19 mRNA vaccine (100 mcg) in preventing COVID-19 disease in people who are living with HIV or have comorbidities associated with elevated risk of severe COVID-19, with the different vaccine regimens assessed determined by whether the participant had evidence of prior SARS-CoV-2 infection at enrollment.
The study is constructed to help inform which vaccine regimen, likely in combination with enhanced HIV care, could serve as a public health model for an effective and cost-efficient approach to preventing SARS-CoV-2 disease, prolonged viral shedding, and the emergence of VOCs within this population. Moreover, we will evaluate whether immune responses postvaccination can be correlated to these clinically important outcomes. The study will enroll 15,600 adults from many clinics in Eastern and Southern Africa. All participants in the study will get the study vaccine. There are 4 primary groups in this study. The groups differ in the number of doses of the study vaccine administered. The groups are organized by whether or not people are living with HIV and whether or not people have evidence of prior SARS-CoV-2 infection in their blood. Group 1 includes people living with HIV and Group 3 includes people who are not living with HIV. All people in groups 1 and 3 will have no evidence of prior SARS-CoV-2 infection in their blood. Participants in Group 1 or Group 3 will get three doses of the study vaccine. Group 2 includes people living with HIV and Group 4 includes people who are not living with HIV. All people in groups 2 and 4 will have evidence of prior SARS-CoV-2 infection in their blood. Participants in Group 2 or Group 4 will get two doses of the study vaccine. There are 8 scheduled clinic visits over 18 months. Study visits may include physical examinations, medical history, vaccine injections, HIV testing, blood collection, nasal swabs, and questionnaires.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Gaborone CRS
Gaborone, Botswana
Eswatini Prevention Center CRS
Mbabane, Hhohho Region, Eswatini
Moi University Clinical Research Centre
Eldoret, Kenya
Kisumu - Kombewa CRS
Kisumu, Kenya
Kisumu Crs
Kisumu, Kenya
Blantyre CRS
Blantyre, Malawi
Malawi CRS
Lilongwe, Malawi
Synergy Biomed Research Institute
East London, Eastern Cape, South Africa
Nelson Mandela Academic Research Unit CRS
Mthatha, Eastern Cape, South Africa
PHOENIX Pharma (Pty) Ltd
Port Elizabeth, Eastern Cape, South Africa
Start Date
December 1, 2021
Primary Completion Date
April 19, 2024
Completion Date
April 19, 2024
Last Updated
November 26, 2025
14,237
ACTUAL participants
Moderna mRNA-1273
BIOLOGICAL
Moderna mRNA-1273.222
BIOLOGICAL
Vaccine 3 Dose
BIOLOGICAL
Vaccine 2 Dose
BIOLOGICAL
Lead Sponsor
COVID-19 Prevention Network
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06631287