In terms of PI, co-formulations of COBI/ATV and COBI/DRV are in development. The low incidence of neuro-psychiatric side

effects with COBI/EVG compared with EFV, and the lower prevalence of diarrhoea with COBI/ATV compared with RTV/ATV, makes it a potentially attractive alternative to these commonly prescribed agents. The reduced pill burden and once-daily administration distinguish COBI/EVG www.selleckchem.com/products/Lapatinib-Ditosylate.html from RTG, the only other II currently licensed. However, a single-tablet regimen based on the investigational integrase, dolutegravir, co-formulated with abacavir and lamivudine is expected to be licensed within the next 12 months and is currently under review by the FDA. Stribild’s lack of interaction with acid-reducing agents distinguishes it from ATV and RPV. There remain several data gaps, and widespread uptake of Stribild and COBI may be hampered by these. The male predominance and high median CD4 cell count of the phase III trial participants limit data in women and YAP-TEAD Inhibitor 1 patients with low CD4 cell counts, opportunistic infections, malignancy or other serious co-morbidities, although the WAVES study, comparing Stribild

to Truvada® (Gilead Inc., Foster City, CA, USA) plus RTV/ATV in women, is currently recruiting. COBI is associated with drug–drug interactions, few of which have been studied to date. Although virological failure with Stribild was uncommon, patients that did fail commonly enough did so with dual-class resistance, and it remains unclear whether these viral isolates remain susceptible to dolutegravir. Also, Stribild selleck is only licensed for use in patients

with creatinine clearance ≥70 mL/min thus is not suitable for patients with renal impairment. The inclusion of TDF in Stribild makes it a less attractive option for patients with, or at risk of, osteoporosis, although the renal and bone concerns are likely to be less if TAF becomes the preferred tenofovir formulation of COBI-based single-tablet regimens. Finally, in an increasingly cost-conscious environment, the relative benefits of Stribild and COBI will have to be weighed against any incremental cost relative to current proprietary medications as well as forthcoming generic formulations. Acknowledgments No funding or sponsorship was received for this study or publication of this article. Frank A. Post is the guarantor for this article, and takes responsibility for the integrity of the work as a whole. Prior to peer review Gilead were offered the opportunity to review the article solely to ensure scientific accuracy of the details. Minor changes were made to the content as a result, at the discretion of the authors. No writing assistance or other editorial involvement was provided by the manufacturer.