Population Pharmacokinetics of Capivasertib in Patients with Advanced or Metastatic Solid Tumours

Capivasertib pharmacokinetics showed moderate between-subject variability, and most covariates assessed had no significant impact. Body weight, dose, concomitant use of paclitaxel, food effect and formulation showed statistically significant effects. However, these were predicted to impact exposure to capivasertib by <20% and were not expected to be clinically relevant. Based on the population pharmacokinetics, no a priori dose adjustment is needed for intrinsic and extrinsic factors.

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Publication Details

Journal
Clinical Pharmacokinetics
Published
2024-08-01
DOI
https://doi.org/10.1007/s40262-024-01407-x
Citations
6
Primary Topic
Advanced Breast Cancer Therapies
Type
article
Field-Weighted Citation Impact
2.51

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article

Population Pharmacokinetics of Capivasertib in Patients with Advanced or Metastatic Solid Tumours

Diansong Zhou, Cath Eberlein, Simon T. Barry, Marie Cullberg et al.
6 citations
Clinical Pharmacokinetics
Advanced Breast Cancer Therapies
2.51
article

Population Pharmacokinetics of Capivasertib in Patients with Advanced or Metastatic Solid Tumours

Diansong Zhou, Cath Eberlein, Simon T. Barry, Marie Cullberg, Carlos Fernández‐Teruel
article en
6 citations

Abstract

Capivasertib pharmacokinetics showed moderate between-subject variability, and most covariates assessed had no significant impact. Body weight, dose, concomitant use of paclitaxel, food effect and formulation showed statistically significant effects. However, these were predicted to impact exposure to capivasertib by <20% and were not expected to be clinically relevant. Based on the population pharmacokinetics, no a priori dose adjustment is needed for intrinsic and extrinsic factors.

Clinical PharmacokineticsVol. 63(8)
AstraZeneca (United Kingdom) (GB), AstraZeneca (Finland) (FI), AstraZeneca (Sweden) (SE), AstraZeneca (United States) (US)
AstraZeneca, Astex Pharmaceuticals
Zero hunger
Openalex Percentile: Top 10%
Advanced Breast Cancer Therapies
2.51
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