Lenacapavir: A Novel, Potent, and Selective First-in-Class Inhibitor of HIV-1 Capsid Function Exhibits Optimal Pharmacokinetic Properties for a Long-Acting Injectable Antiretroviral Agent.

HIV-1 capsid inhibitor PK modeling combination antiretroviral therapy human PK long-acting injectable nonclinical pharmacokinetics

Journal

Molecular pharmaceutics
ISSN: 1543-8392
Titre abrégé: Mol Pharm
Pays: United States
ID NLM: 101197791

Informations de publication

Date de publication:
04 Dec 2023
Historique:
medline: 5 12 2023
pubmed: 2 11 2023
entrez: 2 11 2023
Statut: ppublish

Résumé

Lenacapavir (LEN) is a picomolar first-in-class capsid inhibitor of human immunodeficiency virus type 1 (HIV-1) with a multistage mechanism of action and no known cross resistance to other existing antiretroviral (ARV) drug classes. LEN exhibits a low aqueous solubility and exceptionally low systemic clearance following intravenous (IV) administration in nonclinical species and humans. LEN formulated in an aqueous suspension or a PEG/water solution formulation showed sustained plasma exposure levels with no unintended rapid drug release following subcutaneous (SC) administration to rats and dogs. A high total fraction dose release was observed with both formulations. The long-acting pharmacokinetics (PK) were recapitulated in humans following SC administration of both formulations. The SC PK profiles displayed two-phase absorption kinetics in both animals and humans with an initial fast-release absorption phase, followed by a slow-release absorption phase. Noncompartmental and compartmental analyses informed the LEN systemic input rate from the SC depot and exit rate from the body. Modeling-enabled deconvolution of the input rates from two processes: absorption of the soluble fraction (minor) from a direct fast-release process leading to the early PK phase and absorption of the precipitated fraction (major) from an indirect slow-release process leading to the later PK phase. LEN SC PK showed flip-flop kinetics due to the input rate being substantially slower than the systemic exit rate. LEN input rates via the slow-release process in humans were slower than those in both rats and dogs. Overall, the combination of high potency, exceptional stability, and optimal release rate from the injection depot make LEN well suited for a parenteral long-acting formulation that can be administered once up to every 6 months in humans for the prevention and treatment of HIV-1.

Identifiants

pubmed: 37917742
doi: 10.1021/acs.molpharmaceut.3c00626
pmc: PMC10698746
doi:

Substances chimiques

Anti-Retroviral Agents 0
Anti-HIV Agents 0
Capsid Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6213-6225

Références

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Auteurs

Raju Subramanian (R)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Jennifer Tang (J)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Jim Zheng (J)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Bing Lu (B)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Kelly Wang (K)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Stephen R Yant (SR)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

George J Stepan (GJ)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Andrew Mulato (A)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Helen Yu (H)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Scott Schroeder (S)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Naveed Shaik (N)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Renu Singh (R)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Scott Wolckenhauer (S)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Anne Chester (A)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Winston C Tse (WC)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Anna Chiu (A)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Martin Rhee (M)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Tomas Cihlar (T)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

William Rowe (W)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

Bill J Smith (BJ)

Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, California 94404, United States.

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Classifications MeSH