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Clinical Trial Summary

The primary purpose of this study is to assess the preventive vaccine efficacy (VE), safety and tolerability of a heterologous prime/boost regimen utilizing Ad26.Mos4.HIV and aluminum-phosphate adjuvanted Clade C gp 140 for the prevention of Human Immuno Virus (HIV) infection in HIV-seronegative women residing in sub-Saharan Africa from confirmed HIV-1 infections diagnosed between the Month 7 and Month 24 visits.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03060629
Study type Interventional
Source Janssen Vaccines & Prevention B.V.
Contact
Status Terminated
Phase Phase 2
Start date November 3, 2017
Completion date February 2, 2022

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