Managing Esketamine Treatment Frequency Toward Successful Outcomes: Analysis of Phase 3 Data

Author:

Nijs Michel1,Wajs Ewa2,Aluisio Leah3,Turkoz Ibrahim4,Daly Ella5,Janik Adam3,Borentain Stephane5,Singh Jaskaran B3,DiBernardo Allitia6,Wiegand Frank5

Affiliation:

1. Janssen Research and Development, LLC, Department of Global Analytics – Neuroscience, Titusville

2. Janssen Research and Development, Belgium, Department of Neuroscience, Beerse, Belgium

3. Janssen Research and Development, LLC, Department of Neuroscience, San Diego, CA

4. Janssen Research and Development, LLC, Department of Statistics & Decision Sciences, Titusville, NJ

5. Janssen Research and Development, LLC, Department of Clinical Medical Affairs, Titusville, NJ

6. Janssen Research and Development, France, Department of Clinical Medical Affairs, Issy-les-Moulineaux, France

Abstract

Abstract Background Esketamine nasal spray was recently approved for treatment-resistant depression. The current analysis evaluated the impact of symptom-based treatment frequency changes during esketamine treatment on clinical outcomes. Methods This is a post-hoc analysis of an open-label, long-term (up to 1 year) study of esketamine in patients with treatment-resistant depression (SUSTAIN 2). During a 4-week induction phase, 778 patients self-administered esketamine twice weekly plus a new oral antidepressant daily. In responders (≥50% reduction in Montgomery-Åsberg Depression Rating Scale total score from baseline), esketamine treatment frequency was thereafter decreased during an optimization/maintenance phase to weekly for 4 weeks and then adjusted to the lowest frequency (weekly or every other week) that maintained remission (Montgomery-Åsberg Depression Rating Scale ≤ 12) based on a study-defined algorithm. The relationship between treatment frequency and symptom response, based on clinically meaningful change in Clinical Global Impression–Severity score, was subsequently evaluated 4 weeks after treatment frequency adjustments in the optimization/maintenance phase. Results Among 580 responders treated with weekly esketamine for the first 4 weeks in the optimization/maintenance phase (per protocol), 26% continued to improve, 50% maintained clinical benefit, and 24% worsened. Thereafter, when treatment frequency could be reduced from weekly to every other week, 19% further improved, 49% maintained benefit, and 32% worsened. For patients no longer in remission after treatment frequency reduction, an increase (every other week to weekly) resulted in 47% improved, 43% remained unchanged, and 10% worsened. Conclusions These findings support individualization of esketamine nasal spray treatment frequency to optimize treatment response in real-world clinical practice. Trial Registration ClinicalTrials.gov identifier: NCT02497287

Funder

Janssen Research and Development

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

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