Abstract | BACKGROUND AND OBJECTIVES: METHODS: Plasma concentration-time data were collected from 442 participants (105 healthy volunteers and 337 patients with cancer) who received single or multiple doses of oral brigatinib in one of five trials. Data were analyzed using non-linear mixed-effects modeling (NONMEM software version 7.3). RESULTS:
Brigatinib plasma concentrations were best described by a three-compartment model with a transit compartment input (number of transit compartments = 2.35; mean transit time = 0.9 h). The final model included albumin as a covariate on apparent clearance. None of the additional covariates examined, including sex, age, race, body weight, mild or moderate renal impairment, total bilirubin, aspartate aminotransferase, and alanine aminotransferase, were found to meaningfully explain variability in apparent clearance, suggesting that no dose adjustment is required based on these covariates. CONCLUSIONS: Results from these population pharmacokinetic analyses informed the prescribing guidance for patients with mild or moderate renal impairment in the US Prescribing Information and the European Summary of Product Characteristics for brigatinib.
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Authors | Neeraj Gupta, Xiaohui Wang, Elliot Offman, Marita Prohn, Narayana Narasimhan, David Kerstein, Michael J Hanley, Karthik Venkatakrishnan |
Journal | Clinical pharmacokinetics
(Clin Pharmacokinet)
Vol. 60
Issue 2
Pg. 235-247
(02 2021)
ISSN: 1179-1926 [Electronic] Switzerland |
PMID | 32816246
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Organophosphorus Compounds
- Pyrimidines
- brigatinib
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Topics |
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Clinical Trials as Topic
- Female
- Healthy Volunteers
- Humans
- Male
- Middle Aged
- Neoplasms
(metabolism)
- Organophosphorus Compounds
(pharmacokinetics)
- Pyrimidines
(pharmacokinetics)
- Young Adult
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