Experimental HIV Drugs
ICAAC 2008: Long-term Safety of Investigational CCR5 Antagonist Vicriviroc in Treatment-experienced Patients
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- Category: Experimental HIV Drugs
- Published on Tuesday, 28 October 2008 13:55
- Written by Liz Highleyman
Schering-Plough's investigational CCR5 antagonist vicriviroc has demonstrated potent activity against HIV in laboratory studies and clinical trials of treatment-experienced patients. More than 200 patients received vicriviroc in Phase II trials. In a poster presented at the 48th International Conference on Antimicrobial Agents and Chemotherapy (ICAAC 2008), taking place this week in Washington, DC, researchers described long-term safety data from this population.
AIDS 2008: Investigational Next-generation NNRTI Rilpivirine (TMC278) Demonstrates Potent Antiviral Activity at 96 Weeks in Treatment-naive Patients
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- Category: Experimental HIV Drugs
- Published on Friday, 08 August 2008 13:56
- Written by Liz Highleyman
Tibotec's investigational next-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) rilpivirine (TMC278) has previously demonstrated good efficacy and tolerability in an international Phase 2b trial of treatment-naive patients through 48 weeks. Investigators presented 96-week follow-up data at the XVII International Conference on AIDS taking place this week in Mexico City.
AIDS 2006: TNX-355 Produces Significant Reduction in HIV Viral Load at 48 Weeks
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- Category: Experimental HIV Drugs
- Published on Friday, 25 August 2006 00:00
- Written by Liz Highleyman
Data on several investigational anti-HIV drug candidates were presented at the XVI International AIDS Conference last week in Toronto, including the latest results from a study of Tanox’s investigational monoclonal antibody, TNX-355. TNX-355 is a recombinant human antibody that binds to domain 2 of the CD4 receptor, thereby blocking the entry of HIV into host cells.
Monoclonal Antibody CCR5 Inhibitor PRO 140 Produces Long-lasting HIV Suppression in Single-dose Study
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- Category: Experimental HIV Drugs
- Published on Friday, 28 September 2007 00:00
- Written by Liz Highleyman
In order to enter human CD4 T-cells, HIV must bind to both the CD4 receptor on the cell surface and 1 of 2 co-receptors, CCR5 or CXCR4. If the virus cannot attach to a co-receptor, it cannot infect new cells. The first oral CCR5 antagonist, maraviroc (Selzentry) was recently approved, and another such agent, vicriviroc, has shown promising results in clinical trials.