Hostname: page-component-76fb5796d-x4r87 Total loading time: 0 Render date: 2024-04-25T12:05:07.389Z Has data issue: false hasContentIssue false

Comparison of Safety and Tolerability of Deutetrabenazine During Titration and Maintenance in Patients with Tardive Dyskinesia

Published online by Cambridge University Press:  30 April 2021

Amanda Wilhelm
Affiliation:
Teva Pharmaceutical Industries Ltd., West Chester, PA, USA
Karen E. Anderson
Affiliation:
Georgetown University, Washington, DC, USA
Hubert H. Fernandez
Affiliation:
Cleveland Clinic, Cleveland, OH, USA
Hadas Barkay
Affiliation:
Teva Pharmaceutical Industries Ltd., Netanya, Israel
Nayla Chaijale
Affiliation:
Teva Pharmaceutical Industries Ltd., West Chester, PA, USA
Alexander F. Send
Affiliation:
Teva Pharmaceutical Industries Ltd., West Chester, PA, USA
Juha-Matti Savola
Affiliation:
Teva Pharmaceutical Industries Ltd., Basel, Switzerland
Mark Forrest Gordon
Affiliation:
Teva Pharmaceutical Industries Ltd., West Chester, PA, USA
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Background

Deutetrabenazine is approved to treat tardive dyskinesia (TD) in adults and is titrated weekly by 6 mg/day, from 12 to 48 mg/day, based on dyskinesia control and tolerability. This analysis compared the safety of deutetrabenazine during titration versus maintenance.

Methods

Safety was assessed during titration versus maintenance using integrated data from two 12-week placebo-controlled studies (ARM-TD and AIM-TD) and the open-label extension study. Rates were compared for overall and serious adverse events (AEs), AEs leading to discontinuation, treatment-related AEs, common AEs (≥4%), and specific AEs (parkinsonism, suicidal ideation, akathisia, restlessness).

Results

In titration versus maintenance, AE rates with placebo (n=130) were: overall, 43.1% vs 25.4%; serious, 4.6% vs 2.3%; leading to discontinuation, 3.1% vs 0; treatment-related, 26.9% vs 10.0%. For placebo, common AEs during titration were somnolence, headache, nausea, fatigue, and dry mouth; none occurred during maintenance. In titration versus maintenance, AE rates in fixed-dose deutetrabenazine 12–36 mg (n=216) were: overall, 33.3–38.9% vs 22.2–29.2%; serious, 2.8–6.9% vs 0–1.4%; leading to discontinuation, 2.8–5.6% vs 0; treatment-related, 8.3–16.7% vs 8.3–13.9%. For fixed-dose deutetrabenazine, common AEs during titration were headache, diarrhea, nasopharyngitis, depression, hypertension, and dry mouth; headache was the only common AE during maintenance. In titration versus maintenance, AE rates with flexible-dose deutetrabenazine (n=168) were: overall, 49.4% vs 32.7%; serious, 3.6% vs 2.4%; leading to discontinuation, 2.4% vs 0.6%. For flexible-dose deutetrabenazine, the only common AE during titration was somnolence; none occurred during maintenance. Rates of parkinsonism, suicidal ideation, akathisia, and restlessness were low and comparable in titration and maintenance.

Conclusions

Deutetrabenazine was well-tolerated, with AE rates similar to placebo during both phases; AE rates were higher during titration and decreased during maintenance.

Funding

Teva Pharmaceutical Industries Ltd., Petach Tikva, Israel

Type
Abstracts
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Footnotes

Presenting Author: Amanda Wilhelm