Population Analysis of Anidulafungin in Infants to Older Adults With Confirmed or Suspected Invasive Candidiasis.


Journal

Clinical pharmacology and therapeutics
ISSN: 1532-6535
Titre abrégé: Clin Pharmacol Ther
Pays: United States
ID NLM: 0372741

Informations de publication

Date de publication:
08 2020
Historique:
received: 02 12 2019
accepted: 28 02 2020
pubmed: 20 3 2020
medline: 25 5 2021
entrez: 20 3 2020
Statut: ppublish

Résumé

In a pooled population analysis, we investigated the pharmacokinetics of i.v. anidulafungin in four studies across a full range of adult and pediatric ages in patients with confirmed, suspected, or at high risk of invasive candidiasis (IC). Relationships between anidulafungin exposure and key efficacy end points (global response of success and all-cause mortality) and safety end points (all-cause hepatic or gastrointestinal adverse events) in all patients and separately in pediatric patients and the appropriate dosing regimen for IC treatment in pediatric patients were evaluated. Pediatric patients received a 3.0 mg/kg (maximum 200 mg) i.v. loading dose and 1.5 mg/kg (maximum 100 mg) daily thereafter. Adults received a 200 mg i.v. loading dose and 100 mg daily thereafter. Estimated systemic anidulafungin exposures were similar across age groups (neonates to adults) at the weight-based doses studied in pediatric patients. No clear associations were identified between anidulafungin exposure and efficacy or safety end points.

Identifiants

pubmed: 32189334
doi: 10.1002/cpt.1831
pmc: PMC7485140
doi:

Substances chimiques

Antifungal Agents 0
Anidulafungin 9HLM53094I

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

316-325

Informations de copyright

© 2020 Pfizer Pte Ltd. Clinical Pharmacology & Therapeutics Published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Rujia Xie (R)

Pharmacometrics, Pfizer Asia Manufacturing Pte Ltd, Singapore City, Singapore.

Lynn McFadyen (L)

Pharmacometrics, Pfizer Research and Development UK Ltd, Kent, UK.

Susan Raber (S)

Clinical Pharmacology, Pfizer Inc, La Jolla, California, USA.

Robert Swanson (R)

Clinical Research and Development, Pfizer Inc, Groton, Connecticut, USA.

Margaret Tawadrous (M)

Global Product Development, Pfizer Inc, Groton, Connecticut, USA.

Heidi Leister-Tebbe (H)

Clinical Research and Development, Pfizer Inc, Groton, Connecticut, USA.

Michael Cohen-Wolkowiez (M)

Duke Clinical Research Institute, Durham, North Carolina, USA.
Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.

Daniel K Benjamin (DK)

Duke Clinical Research Institute, Durham, North Carolina, USA.
Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.

Ping Liu (P)

Formerly Clinical Pharmacology, Development China, Pfizer Inc, Beijing, China.

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Classifications MeSH