Pharmacokinetic and Pharmacodynamic Comparison of Once‐Daily Efavirenz (400 mg vs. 600 mg) in Treatment‐Naïve HIV‐Infected Patients: Results of the ENCORE1 Study

Author:

Dickinson L1,Amin J2,Else L1,Boffito M3,Egan D1,Owen A1,Khoo S1,Back D1,Orrell C4,Clarke A5,Losso M6,Phanuphak P5,Carey D2,Cooper DA2,Emery S2,

Affiliation:

1. Department of Molecular & Clinical PharmacologyUniversity of LiverpoolLiverpool UK

2. Kirby InstituteUNSW AustraliaSydney Australia

3. Chelsea & Westminster Foundation TrustLondon UK

4. Desmond Tutu HIV FoundationCape Town South Africa

5. HIV‐NAT Thai Red Cross AIDS Research CenterBangkok Thailand

6. Hospital Ramos MejíaBuenos Aires Argentina

Funder

ENCORE1 substudies were funded through a project grant from the Australian Government National Health and Medical Research Council (NHMRC)

The Kirby Institute is funded in part by the Australian Government Department of Health and Ageing

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference42 articles.

1. World Health Organisation.Global update on HIV treatment 2013: results impact and opportunities. (2013). Accessed 10 September 2014.

2. World Health Organisation.Key facts on global HIV epidemic and progress in 2010. (2011). Accessed 9 September 2014.

3. World Health Organisation.Consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV infection. Recommendations for a public health approach. (2013). Accessed 9 September 2014.

4. Haas D.W.et al.A phase II double‐blind placebo‐controlled dose ranging study to assess the antiretroviral activity and safety of efavirenz in combination with open‐label zidovudine with lamivudine at 36 weeks [DMP 266‐005]. The XII International AIDS Conference Geneva Switzerland. Abstract 22334 (1998).

5. Efficacy of 400 mg efavirenz versus standard 600 mg dose in HIV-infected, antiretroviral-naive adults (ENCORE1): a randomised, double-blind, placebo-controlled, non-inferiority trial

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