Pharmacokinetics, Safety and Antiviral Activity of Fosamprenavir/Ritonavir-containing Regimens in HIV-infected Children Aged 4 Weeks to 2 Years—48-week Study Data

Author:

Cotton Mark,Cassim Haseena,Pavía-Ruz Noris,Garges Harmony P.,Perger Teodora,Ford Susan L.,Wire Mary Beth,Givens Naomi,Ross Lisa L.,Lou Yu,Sievers Jörg,Cheng Katharine

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Microbiology (medical),Pediatrics, Perinatology and Child Health

Reference12 articles.

1. The NEAT Study: A 48-week open-label study to compare the antiviral efficacy and safety of GW43908 versus nelfinavir in antiretroviral therapy-naive HIV-1-infected patients.;Rodriguez-French;JAIDS,2004

2. SOLO: 48-week efficacy and safety comparison of once-daily fosamprenavir ritonavir versus twice-daily nelfinavir in naive HIV-1-infected patients.;Gathe;AIDS,2004

3. Pharmacokinetics of fosamprenavir plus ritonavir in human immunodeficiency virus type 1-infected adult subjects with hepatic impairment.;Perez-Elias;Antimicrob Agents Chemother,2009

4. Pharmacokinetic modeling and simulations of interaction of amprenavir and ritonavir.;Sale;Antimicrob Agents Chemother,2002

5. Pharmacokinetics and safety of amprenavir and ritonavir following multiple-dose co-administration to healthy volunteers.;Sadler;AIDS,2001

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