Evaluation of the pharmacokinetic drug-drug interaction between the antiretroviral agents fostemsavir and maraviroc: a single-sequence crossover study in healthy participants
Author:
Affiliation:
1. ViiV Healthcare, Research Triangle Park, NC, USA;
2. GlaxoSmithKline, Upper Providence, PA, USA
3. ViiV Healthcare, Branford, CT, USA
Publisher
Informa UK Limited
Link
https://www.tandfonline.com/doi/pdf/10.1080/25787489.2021.2016301
Reference25 articles.
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2. Nettles RE Chien C Elefant E et al. Single and multiple dose pharmacokinetics and safety in non‐HIV‐infected healthy subjects dosed with BMS‐663068 an oral HIV attachment inhibitor. Paper presented at: 12th International Workshop on Clinical Pharmacology of HIV Therapy; April 13–15 2011; Miami FL. Abstract O_04.
3. Homology models of the HIV-1 attachment inhibitor BMS-626529 bound to gp120 suggest a unique mechanism of action
4. Crystal structures of trimeric HIV envelope with entry inhibitors BMS-378806 and BMS-626529
5. Lataillade M Krystal M Ackerman P. Conceptualization and design of mechanism of action for temsavir. Paper presented at: 16th European AIDS Conference; October 25–27 2017; Milan Italy. Abstract.
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1. Consensus recommendations for the use of novel antiretrovirals in persons with HIV who are heavily treatment‐experienced and/or have multidrug‐resistant HIV‐1: Endorsed by the American Academy of HIV Medicine, American College of Clinical Pharmacy;Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy;2024-05
2. Mechanism of action, resistance, interaction, pharmacokinetics, pharmacodynamics, and safety of fostemsavir;BMC Infectious Diseases;2024-02-23
3. Model‐Based Dose Selection of Fostemsavir for Pediatric Populations With Multidrug‐Resistant HIV‐1 and Relative Bioavailability Assessment in Healthy Adults;Clinical Pharmacology in Drug Development;2023-06-17
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