Viewing Study NCT01144026



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Study NCT ID: NCT01144026
Status: COMPLETED
Last Update Posted: 2013-01-18
First Post: 2010-06-12

Brief Title: Clinical Study of TUTI-16 in HIV-1 Infected and Uninfected Subjects
Sponsor: Thymon LLC
Organization: Thymon LLC

Study Overview

Official Title: Phase IIIA Clinical Study of TUTI-16 in HIV-1 Infected and Uninfected Subjects
Status: COMPLETED
Status Verified Date: 2013-01
Last Known Status: None
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: THYMON-10001
Brief Summary: This protocol represents the second in human study of TUTI-16 and is being conducted to continue to gather safety and human immunogenicity anti-HIV-1 Tat titers data of subcutaneously administered TUTI-16
Detailed Description: HIV-1 Tat protein a virally encoded toxin is secreted by HIV-1 infected cells and acts on uninfected cells rendering them permissive for HIV-1 replication HIV-1 Tat enhances chronic viral replication and induces immune suppression Antibodies to Tat inhibit this Tat-mediated transcellular activation in vitro and minimize chronic plasma viremia HIV-1 Tat activities can be blocked in vitro and in vivo by anti-Tat antibodies

The Thymon Universal Tat Immunogen TUTI-16 is a fully synthetic self-adjuvanting lipopeptide vaccine that is water soluble and administered by subcutaneous injection In preclinical studies a priming dose and a three week boost in rats induced a high titer antibody response to the eight known distinct epitope variants of HIV-1 Tat protein These antibodies block the function of the HIV-1 Tat protein toxin which is essential to the maintenance of chronic HIV-1 viremia Therefore TUTI-16 has potential as a therapeutic vaccine for HIV-1 in humans

Study Oversight

Has Oversight DMC: None
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?: None