Population Pharmacokinetic and Exposure-Response Analyses for Efficacy and Safety of Risankizumab in Patients With Active Crohn's Disease.


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:
04 2023
Historique:
received: 01 09 2022
accepted: 11 12 2022
pubmed: 20 12 2022
medline: 17 3 2023
entrez: 19 12 2022
Statut: ppublish

Résumé

The population pharmacokinetics (PK) of risankizumab and exposure-response relationships for efficacy and safety in patients with Crohn's disease (CD) were characterized using data from phase II and III studies to support dosing regimen selection. A two-compartment model with first-order absorption and first-order elimination adequately described risankizumab PK. Covariates including sex, baseline fecal calprotectin, corticosteroid use, baseline creatinine clearance, body weight, and baseline albumin were statistically correlated with risankizumab clearance, but their impact on exposure was not clinically relevant for efficacy or safety. Exposure-response analyses showed that exposures associated with the 600 mg intravenous (i.v.) induction dose at Weeks 0, 4, and 8 achieved a near maximal response for all efficacy end points evaluated, with negligible added benefit from the 1,200 mg i.v. regimen. By Week 52 of the maintenance treatment, trends of higher responses were observed for the exposure range associated with the 360 mg subcutaneous (s.c.) every-8-weeks (Q8W) regimen for most of the evaluated efficacy end points, particularly for the more stringent end points, such as endoscopic remission and ulcer-free endoscopy. Exposure-response analyses for safety did not identify any apparent relationship between exposure and safety. These results supported the final dose recommendation of 600 mg i.v. at Weeks 0, 4, and 8, followed by 360 mg s.c. at Week 12 and Q8W thereafter in patients with CD.

Identifiants

pubmed: 36534322
doi: 10.1002/cpt.2831
doi:

Substances chimiques

risankizumab 90ZX3Q3FR7
Antibodies, Monoclonal 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

839-850

Informations de copyright

© 2022 AbbVie Inc. Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Ahmed Abbas Suleiman (AA)

Clinical Pharmacology, AbbVie Deutschland GmbH & Co KG, Ludwigshafen, Germany.

Aline Goebel (A)

Clinical Pharmacology, AbbVie Deutschland GmbH & Co KG, Ludwigshafen, Germany.

Sumit Bhatnagar (S)

Clinical Pharmacology, AbbVie Inc, North Chicago, Illinois, USA.

Ronilda D'Cunha (R)

Clinical Pharmacology, AbbVie Inc, North Chicago, Illinois, USA.

Wei Liu (W)

Clinical Pharmacology, AbbVie Inc, North Chicago, Illinois, USA.

Yinuo Pang (Y)

Clinical Pharmacology, AbbVie Inc, North Chicago, Illinois, USA.

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