| Abstract | Patients with on-going HIV-1 replication and a K65R mutation in HIV-1 RT were assessed for further development of RT mutations while taking tenofovir disoproxil fumarate and other antiretroviral drugs. K65R was observed in 10 out of 536 treatment-experienced patients entering the study. K65R became undetectable in two patients, and the development of additional resistance mutations was minimal. Over 18 months, no patient developed multinucleoside resistance (Q151M or T69 insertions) and plasma viral loads were stable (median +0.04 log10 copies/ml). |
| Authors | Brandi J Chappell, Nicolas A Margot, Michael D Miller
(Affiliation: Gilead Sciences, Inc., Foster City, California 94404, USA.)
|
| Journal | AIDS (London, England)
(AIDS)
Vol. 21
Issue 6
Pg. 761-3
(Mar 30 2007)
ISSN: 0269-9370 England |
| PMID | 17413698
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
| Chemical References |
- Anti-HIV Agents
- Anti-Retroviral Agents
- Phosphonic Acids
- RNA, Viral
- Reverse Transcriptase Inhibitors
- tenofovir disoproxil
- Adenine
- RNA-Directed DNA Polymerase
|
| Topics |
- Adenine
(analogs & derivatives, therapeutic use)
- Anti-HIV Agents
(therapeutic use)
- Anti-Retroviral Agents
(therapeutic use)
- Drug Resistance, Viral
(genetics)
- Drug Therapy, Combination
- HIV Infections
(drug therapy, virology)
- HIV-1
(enzymology, genetics)
- Humans
- Long-Term Care
- Longitudinal Studies
- Mutation
- Phosphonic Acids
(therapeutic use)
- RNA, Viral
(blood)
- RNA-Directed DNA Polymerase
(genetics)
- Reverse Transcriptase Inhibitors
(therapeutic use)
- Treatment Outcome
- Viral Load
|
