CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 48 enrolled
Drug / intervention
SAAVI DNA-C2 vaccine +2 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00574600
NCT00574600Phase 1Completed

A Phase 1 Placebo-controlled Clinical Trial to Evaluate the Safety and Immunogenicity of SAAVI DNA-C2 Vaccine Boosted by SAAVI MVA-C Vaccine, in HIV Uninfected Healthy Vaccinia Naive Adult Participants in South Africa and the United States

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Dec 17, 2007·Updated Oct 14, 2021

In Brief

A Phase 1 clinical trial evaluating SAAVI DNA-C2 vaccine, SAAVI MVA-C vaccine, and 1 other intervention for HIV Infections. Completed, enrolled 48 participants across 4 sites in 2 countries.

Detailed Summary

The purpose of this study is to evaluate the safety of and immune response to an experimental DNA HIV vaccine followed by boosting with an experimental modified vaccinia HIV vaccine (MVA) in HIV uninfected adults.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHIV Infections
CountriesSouth Africa, United States

Timeline

Phase 1CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 17, 2007
Enrollment StartNov 1, 2008
Primary CompletionOct 1, 2010
Study CompletionJan 1, 2013
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 18.5 years ago

Interventions

SAAVI DNA-C2 vaccinebiological

DNA vaccine

SAAVI MVA-C vaccinebiological

Boost vaccine

Placebobiological

Placebo vaccine