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Sisonke (Together): OPEN LABEL TRIAL Open-label, single-arm phase 3B implementation study to monitor the effectiveness of the single-dose Ad26.COV2.S COVID-19 vaccine among health care workers in South Africa (VAC31518COV3012

Sisonke (Together): OPEN LABEL TRIAL Open-label, single-arm phase 3B implementation study to monitor the effectiveness of the single-dose Ad26.COV2.S COVID-19 vaccine among health care workers in South Africa (VAC31518COV3012

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
PACTR
Registry ID
PACTR202102855526180
Enrollment
500000
Registered
2021-02-15
Start date
2021-03-01
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid-19

Interventions

Ad26 COV2S by Janssen administered as a single injection
Not applicable

Sponsors

South African Medical 7505 Council
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria Age 18 and older Health care worker in the private or public service The President and Deputy President of South africa (*The President and Deputy President of South Africa have been included in the protocol to address the issue of vaccine hesitancy.) Willingness and ability to comply vaccination plan and other study procedures. Capable of giving electronic or personal signed informed consent as described in Appendix 5, which includes compliance with the requirements in this protocol. Inclusion criteria for the sub-cohort Age 18 and older Health care worker in the private or public service Willingness and ability to comply with all scheduled visits, vaccination plan, laboratory tests, and other study procedures, with follow-up at an ENSEMBLE site. Capable of giving electronic or personal signed informed consent as described in Appendix 5, which includes compliance with the requirements in this protocol.

Exclusion criteria

Exclusion criteria: Exclusion criteria Any significant acute or chronic medical condition, situation or circumstance that in the opinion of the PI/designee makes the participant unsuitable for participation in the study, or jeopardises the safety or rights of the participant Known pregnancy Current participation in any other research studies that would interfere with the objectives of this study. The determination of whether participation in another study would be exclusionary for a given participant will be made by the PI/designee History of severe adverse reaction associated with a vaccine and/or severe allergic reaction (e.g., anaphylaxis) to any component of the vaccine. Immunosuppressive therapy, including cytotoxic agents or systemic corticosteroids, e.g., for cancer or an autoimmune disease, or planned receipt throughout the stud

Design outcomes

Primary

MeasureTime frame
Rates of hospitalizations and deaths among vaccinated HCWs versus general unvaccinated population

Secondary

MeasureTime frame
To estimate the incidence of symptomatic SARS CoV-2 infections among vaccinated HCWs To monitor the genetic diversity of breakthrough SARS CoV-2 infections To measure serum neutralization and T-cell responses among vaccinees (estimated sub-set of 10,000) To monitor for asymptomatic infection in a sub-set of HCWs To conduct pharmacovigilance to monitor for safety and any unexpected adverse effects of the vaccine administration To estimate vaccine uptake among HCWs in South Africa

Countries

South Africa

Contacts

Public ContactFatima Mayat

Implementation and Operational Support

mayatf@phru.co.za00279899798

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026