The 48-week design of the current study will allow the ability of ATC to select for resistance mutations to be assessed over a longer period. All patients who could be genotyped at

day 21 (n=38) maintained the M184V mutation. In vitro studies have previously shown that the M184V selleck screening library mutation is maintained when viruses containing the mutation are cultured under ATC drug pressure [12]. The M184V mutation is associated with reduced replicative fitness compared with the wild-type sequence [13,14]. Maintenance of the M184V mutation is therefore of potential benefit. Whether the M184V mutation is maintained over periods of ATC treatment longer than 21 days will be assessed at later time-points in Regorafenib supplier the study. ATC appeared to be very well tolerated over the 21-day treatment period, at both the 600 and 800 mg bid doses. Few AEs, none of them serious, were reported during this treatment period. The AEs related to ATC were mostly gastrointestinal in nature and mild in severity, and the treatment-emergent AEs in the two ATC treatment groups were similar to those observed in the 3TC treatment group. In particular, there was no evidence of hyperlipasaemia, liver toxicity, pancreatitis, anaemia, hypersensitivity, mitochondrial toxicity or renal toxicity, which have

been associated with other NRTIs, although longer exposure will be needed to confirm this. ATC provided significant antiviral activity over a 21-day period in treatment-experienced HIV-1-infected patients with the M184V mutation, with or without additional TAMs, who were failing treatment with 3TC. The safety and tolerability of ATC were similar to those of 3TC and there was no evidence of development of novel resistance mutations.

The activity of ATC was greatest in the presence of M184V alone, but still significant Cell press in the presence of TAMs. Thus, over the 21-day treatment period, ATC showed promising antiviral activity that was very well tolerated in treatment-experienced HIV-1-infected patients with reverse transcriptase mutations that confer resistance to other NRTIs. The study was sponsored by Avexa Limited. “
“Patients starting highly active antiretroviral therapy (HAART) may have a suboptimal CD4 increase despite rapid virological suppression. The frequency and the significance for patient care of this discordant response are uncertain. This study was designed to determine the incidence of a discordant response at two time-points, soon after 6 months and at 12 months, and to determine the relationship with clinical outcomes. Data obtained in the UK Collaborative HIV Cohort Study were analysed. A total of 2584 treatment-naïve patients starting HAART with HIV viral load (VL)>1000 HIV-1 RNA copies/mL at baseline and <50 copies/mL within 6 months were included in the analysis.