drugset / Trial / NCT00757250

Safety Study of TXA127 to Elevate CD4+ T-Lymphocyte Counts in HIV-Infected Patients on Stable HAART Therapy

NCT00757250

Phase 1 Terminated 13 enrolled US Biotest, Inc. Tarix Pharmaceuticals · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to test the safety of an investigational medication, TXA127, and its ability to increase T-lymphocyte counts, specifically CD4+ T-lymphocytes, in persons infected with human immunodeficiency virus who are taking highly active anti-retroviral therapy.

Timeline

Start
2008-09
Primary completion
2011-12
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Subject talfirastide Peptide 50 ug/kg Subcutaneous
Subject talfirastide Peptide 100 ug/kg Subcutaneous
Subject talfirastide Peptide 200 ug/kg Subcutaneous
Subject talfirastide Peptide 300 ug/kg Subcutaneous