Population Pharmacokinetic Modeling and Simulation of TV-46000: A Long-Acting Injectable Formulation of Risperidone.

LAI TV-46000 dose selection long-acting injectable modeling and simulations population pharmacokinetics risperidone schizophrenia

Journal

Clinical pharmacology in drug development
ISSN: 2160-7648
Titre abrégé: Clin Pharmacol Drug Dev
Pays: United States
ID NLM: 101572899

Informations de publication

Date de publication:
07 2022
Historique:
received: 04 11 2021
accepted: 29 12 2021
pubmed: 5 3 2022
medline: 6 7 2022
entrez: 4 3 2022
Statut: ppublish

Résumé

TV-46000 is a long-acting subcutaneous antipsychotic that uses a novel copolymer drug delivery technology in combination with a well-characterized molecule, risperidone, that is in clinical development as a treatment for schizophrenia. A population pharmacokinetic (PPK) modeling and simulation approach was implemented to identify TV-46000 doses and dosing schedules for clinical development that would provide the best balance between clinical efficacy and safety. The PPK model was created by applying pharmacokinetic data from a phase 1 study of 97 patients with a diagnosis of schizophrenia or schizoaffective disorder who received either single or repeated doses of TV-46000. The PPK model was used to characterize the complex release profile of the total active moiety (TAM; the sum of the risperidone and 9-OH risperidone concentrations) concentration following subcutaneous injections of TV-46000. The PK profile was best described by a double Weibull function of the in vivo release rate and by a 2-compartment disposition and elimination model. Simulations were performed to determine TV-46000 doses and dosing schedules that maintained a median profile of TAM concentrations similar to published TAM exposure following oral risperidone doses that have been correlated to a 40% to 80% dopamine-D2 receptor occupancy therapeutic window. The simulations showed that therapeutic dose ranges for TV-46000 are 50 to 125 mg for once-monthly and 100 to 250 mg for the once every 2 months regimens. This PPK model provided a basis for prediction of patient-specific exposure and dopamine-D2 receptor occupancy estimates to support further clinical development and dose selection for the phase 3 studies.

Identifiants

pubmed: 35245409
doi: 10.1002/cpdd.1078
pmc: PMC9315033
doi:

Substances chimiques

Antipsychotic Agents 0
Delayed-Action Preparations 0
Receptors, Dopamine D2 0
Risperidone L6UH7ZF8HC
Paliperidone Palmitate R8P8USM8FR

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

865-877

Informations de copyright

© 2022 Teva Pharmaceutical Industries, Ltd. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology.

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Auteurs

Itay Perlstein (I)

Magic Wand Research LLC, Philadelphia, Pennsylvania, USA.

Avia Merenlender Wagner (A)

Teva Branded Pharmaceutical Products Inc. Research and Development, Netanya, Israel.

Roberto Gomeni (R)

Pharmacometrica, Lieu-Dit Longcol, La Fouillade, France.

Michael Lamson (M)

Nuventra Pharma Sciences, Carrboro, North Carolina, USA.

Eran Harary (E)

Teva Branded Pharmaceutical Products Inc. Research and Development, Netanya, Israel.

Ofer Spiegelstein (O)

Teva Branded Pharmaceutical Products Inc. Research and Development, Netanya, Israel.

Attila Kalmanczhelyi (A)

Teva Pharmaceuticals Ltd., Debrecen, Hungary.

Ryan Tiver (R)

Teva Branded Pharmaceutical Products Inc., West Chester, Pennsylvania, USA.

Pippa Loupe (P)

Teva Branded Pharmaceutical Products Inc., West Chester, Pennsylvania, USA.

Micha Levi (M)

Formerly Teva Branded Pharmaceutical Products, currently Bill & Melinda Gates Medical Research Institute, Cambridge, MA, USA.

Anna Elgart (A)

Teva Branded Pharmaceutical Products Inc. Research and Development, Netanya, Israel.

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