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27 A New Method for Initiating Treatment with the Long-acting Antipsychotic Aripiprazole Lauroxil

Published online by Cambridge University Press:  12 March 2019

Jonathan Meyer
Affiliation:
Clinical Professor of Psychiatry, University of California, San Diego, CA
Rakesh Jain
Affiliation:
Clinical Professor, Department of Psychiatry, Texas Tech Health Sciences Center School of Medicine, Midland, TX
Angela Wehr
Affiliation:
Associate Director, Clinical Pharmacology, Alkermes Inc., Waltham, MA
Bhaskar Rege
Affiliation:
Head of Clinical Pharmacology & Translational Medicine, Alkermes Inc., Waltham, MA
Lisa von Moltke
Affiliation:
Head of Clinical Development, Alkermes Inc., Waltham, MA
Peter J Weiden
Affiliation:
Schizophrenia Lead, Medical Affairs, Alkermes Inc., Waltham, MA
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Abstract

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STUDY OBJECTIVE

Slow release is a fundamental feature of long-acting injectable (LAI) antipsychotics. This property allows continuous drug exposure between dosing intervals. However, there can be a significant delay between giving the first LAI dose and achievement of efficacious plasma concentrations. This time period requires additional pharmacologic intervention. Until now, this delay was addressed with one of two strategies: 1) continuing with supplemental oral antipsychotic, or 2) giving more LAI up front (e.g. loading dose). A third strategy has now been developed to reduce the time needed for oral supplementation when starting the LAI aripiprazole lauroxil (AL) from 21days to 1day. A nano-crystalline milled dispersion of AL (ALNCD; brand name ARISTADA INITIO™) was formulated by reducing the AL particle diameter from micron-size particles to nanometer- sized particles. ALNCD has faster dissolution and a shorter half-life than AL and is designed to be used as a single injection along with a single oral aripiprazole dose of 30mg as a 1-day alternative to the 21days of oral aripiprazole supplementation. Here we provide an overview of the new 1-day initiation regimen for starting AL treatment, and demonstrate the relative contributions of each of its components.

METHODS

A blinded, randomized, phase 1, pharmacokinetic (PK), and safety study compared the 1-day initiation regimen with the 21-day oral aripiprazole regimen. A combination of observed data, and population pharmacokinetic model–based simulations were used to plot plasma aripiprazole concentrations of single doses of ALNCD, 30mg oral aripiprazole, and AL, individually, and all three combined.

RESULTS

The PK profiles of the 1-day and 21-day initiation regimens (both in conjunction with either 441mg or 882mg doses of AL) were comparable, with therapeutically relevant aripiprazole levels achieved within 4days of treatment initiation. The safety profile of the 1-day initiation regimen was similar to the 21-day initiation regimen, and consistent with that of AL. Aripiprazole concentration–time profiles demonstrated that each component delivered aripiprazole to the systemic circulation at different time periods, with the 30mg dose of oral aripiprazole predominant in the first week, followed by ALNCD, and then AL.

CONCLUSIONS

The 1-day initiation regimen is well-tolerated and a suitable alternative to 21days of oral aripiprazole supplementation for starting AL. Each component of the 1-day initiation regimen, together with AL, is necessary to provide continuous coverage from treatment initiation until the next regularly scheduled AL injection.

Funding Acknowledgements: This study was funded by Alkermes Inc.

Type
Abstracts
Copyright
© Cambridge University Press 2019