drugset / Trial / NCT00000972

A Phase I Clinical Trial to Evaluate: Part A. The Safety of MTP-PE/MF59 Adjuvant Emulsion. Part B. The Safety and Immunogenicity of Env 2-3, a Yeast Derived Recombinant Envelope Protein of Human Immunodeficiency Virus-1, in Combination With MTP-PE/MF59

NCT00000972

RandomizedPrevention

Summary

To evaluate the safety of a fixed antigen dose with an increasing dose of adjuvant (MTP-PE/MF59, a substance to enhance the immune response to vaccine) in volunteers. To evaluate local and systemic reactions (Part A). To determine the safety and immunogenicity of Env 2-3 in combination with MTP-PE/MF59 in volunteers (Part B). The vaccine Env 2-3 is created from one of the viral proteins that make up HIV called envelope glycoprotein gp120. A problem with many immunogens, including candidate HIV vaccines, is that they may evoke relatively weak immune responses, particularly in humans and in nonhuman primates. Thus, there is considerable interest in the development of "adjuvants" (substances that augment immune responses to vaccines). MTP-PE/MF59 is an adjuvant that appears to be particularly promising, and is selected for the studies with this HIV vaccine candidate.

Timeline

Start
Primary completion
Completion
1992-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Env 2-3 Vaccine
Subject MTP-PE/MF59 Other / unclassified 0 ug
Subject MTP-PE/MF59 Other / unclassified 5 ug
Subject MTP-PE/MF59 Other / unclassified 10 ug
Subject MTP-PE/MF59 Other / unclassified 25 ug
Subject MTP-PE/MF59 Other / unclassified 50 ug
Subject MTP-PE/MF59 Other / unclassified 100 ug