Viewing Study NCT01435135


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Study NCT ID: NCT01435135
Status: UNKNOWN
Last Update Posted: 2020-11-03
First Post: 2011-09-08
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Study of Late Boost Strategies for HIV-uninfected Participants From Protocol RV 144
Sponsor: U.S. Army Medical Research and Development Command
Organization:

Study Overview

Official Title: Randomized, Double Blind Evaluation of Late Boost Strategies for HIV-uninfected Participants in the HIV Vaccine Efficacy Trial RV 144: "Aventis Pasteur Live Recombinant ALVAC-HIV (vCP1521) Priming With VaxGen gp120 B/E (AIDSVAX B/E) Boosting in HIV-uninfected Thai Adults"
Status: UNKNOWN
Status Verified Date: 2020-11
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to assess safety and tolerability of late boost regimens of AIDSVAX B/E alone, ALVAC-HIV alone, or ALVAC-HIV/AIDSVAX B/E combination in HIV-uninfected participants from RV 144.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
WRAIR #1792 OTHER WRAIR IRB View
A-14430.13 OTHER USAMRMC HRPO View
S-10-0010 OTHER Sponsor View