TAK-220, a Novel Small-Molecule CCR5 Antagonist, Has Favorable Anti-Human Immunodeficiency Virus Interactions with Other Antiretrovirals In Vitro
Open Access
- 1 August 2005
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 49 (8) , 3483-3485
- https://doi.org/10.1128/aac.49.8.3483-3485.2005
Abstract
TAK-220 is a CCR5 antagonist, part of the new class of anti-human immunodeficiency virus type 1 (anti-HIV-1) entry inhibitors. We evaluated the anti-HIV-1 interactions between TAK-220 and various antiretrovirals in vitro. Synergy was observed with all drugs at the 90 and 95% inhibitory concentrations. The favorable drug interactions observed suggest that further clinical evaluation is warranted.Keywords
This publication has 16 references indexed in Scilit:
- Highly Potent Inhibition of Human Immunodeficiency Virus Type 1 Replication by TAK-220, an Orally Bioavailable Small-Molecule CCR5 AntagonistAntimicrobial Agents and Chemotherapy, 2005
- Viral Entry DeniedNew England Journal of Medicine, 2004
- Treatment for Adult HIV InfectionJAMA, 2004
- Favorable Interactions between Enfuvirtide and 1-β- d -2,6-Diaminopurine Dioxolane In VitroAntimicrobial Agents and Chemotherapy, 2003
- Anti-Human Immunodeficiency Virus Interactions of SCH-C (SCH 351125), a CCR5 Antagonist, with Other Antiretroviral Agents In VitroAntimicrobial Agents and Chemotherapy, 2002
- Strong in Vitro Synergy Between the Fusion Inhibitor T-20 and the CXCR4 Blocker AMD-3100JAIDS Journal of Acquired Immune Deficiency Syndromes, 2000
- In Vivo Antagonism with Zidovudine plus Stavudine Combination TherapyThe Journal of Infectious Diseases, 2000
- Lamivudine or Stavudine in Two- and Three-Drug Combinations against Human Immunodeficiency Virus Type 1 Replication In VitroThe Journal of Infectious Diseases, 1996
- Drug interactions with zidovudine phosphorylation in vitroAntimicrobial Agents and Chemotherapy, 1995
- Three-Drug Synergistic Inhibition of HIV-l Replication In Vitro by Zidovudine, Recombinant Soluble CD4, and Recombinant Interferon-alpha AThe Journal of Infectious Diseases, 1990