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Safety, Tolerability, Pharmacokinetics, and Acceptability of Oral and Long-Acting Cabotegravir in HIV-Negative Chinese Men.
Han, Kelong; Wannamaker, Paul; Lu, Hongzhou; Zhu, Biao; Wang, Meixia; Paff, Melanie; Spreen, William R; Ford, Susan L.
Afiliação
  • Han K; GlaxoSmithKline, Collegeville, Pennsylvania, USA.
  • Wannamaker P; ViiV Healthcare, Research Triangle Park, North Carolina, USA.
  • Lu H; Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
  • Zhu B; The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Wang M; State Drug Clinical Trial Institution, Beijing Youan Hospital, Capital Medical University, Beijing, China.
  • Paff M; GlaxoSmithKline, Collegeville, Pennsylvania, USA.
  • Spreen WR; ViiV Healthcare, Research Triangle Park, North Carolina, USA.
  • Ford SL; GlaxoSmithKline, Research Triangle Park, North Carolina, USA.
Antimicrob Agents Chemother ; 66(3): e0205721, 2022 03 15.
Article em En | MEDLINE | ID: mdl-35129374
Long-acting (LA) cabotegravir demonstrated superior efficacy versus daily oral standard-of-care for HIV-1 preexposure prophylaxis. This phase 1 study assessed safety, tolerability, pharmacokinetics, and acceptability of cabotegravir in 47 HIV-negative adult Chinese men at low risk of acquiring HIV-1. Participants received once-daily oral cabotegravir 30 mg for 4 weeks and, after a 1-week washout, five 600-mg (3-mL) intramuscular cabotegravir LA injections at weeks 5, 9, 17, 25, and 33. Pharmacokinetic plasma samples were intensively collected on day 27 (n = 17) and sparsely collected before each injection until 56 weeks after final injection (n = 47). Cabotegravir LA injections were acceptable and well tolerated. Common adverse events included injection site pain, injection site swelling, and upper respiratory tract infection. No drug-related serious adverse events or deaths occurred. Mean cabotegravir concentration remained above 1.33 µg/mL (8× in vitro protein-adjusted concentration for 90% of the maximum inhibition of viral growth [PA-IC90]) before each injection and above 0.166 µg/mL (PA-IC90) for >32 weeks after final injection. Trough concentrations remained above PA-IC90 in nearly all participants and showed minimal accumulation. Noncompartmental pharmacokinetic analysis was performed. Geometric mean of terminal half-life was 1.89 and 47 days after oral and LA dosing, respectively. Cabotegravir concentrations were estimated to remain quantifiable for 48.7 weeks after final injection. Steady-state area under the concentration-time curve (AUC), peak concentration, trough concentration, terminal half-life, time to peak concentration, and apparent clearance after cabotegravir oral and LA dosing were similar to those estimated in non-Asian men in historical studies. These results support further clinical development of cabotegravir LA in China. (This study has been registered at ClinicalTrials.gov under registration no. NCT03422172.).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Fármacos Anti-HIV Limite: Adult / Humans / Male Idioma: En Revista: Antimicrob Agents Chemother Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Fármacos Anti-HIV Limite: Adult / Humans / Male Idioma: En Revista: Antimicrob Agents Chemother Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos