Apomorphine Injection Significantly Reduces Time to On in Parkinson Disease
The study included patients with Parkinson disease receiving treatment with levodopa carbidopa who experienced morning akinesia.
Results of an open-label study assessing the effect the subcutaneous apomorphine (Apokyn; US WorldMeds) showed that injection of the drug significantly reduced time-to-on in patients with Parkinson disease who experienced delayed onset of morning levodopa.
The study, which was presented at the
Patients recorded their time-to-on during a 7-day treatment period in which apomorphine was injected each morning. Difference in time-to-on between the treatment and baseline periods was the primary end point. Secondary end points included change on global impression scales, as well as safety and tolerability.
During the treatment period, patients achieved a mean time-to-on of 23.72 minutes compared with 60.86 minutes during the baseline period (P <.0001). Time-to-on greater than 60 minutes was more often recorded in patients who received only levodopa versus levodopa plus apomorphine (46% vs 7%). In addition, significant improvement in global impression scaled were recorded from levodopa baseline to the apomorphine treatment period (all P <.0001). Patients most commonly reported nausea and dizziness, with most of those discontinuing therapy due to adverse events during the titration phase.
Overall, patients treated with subcutaneous apomorphine injection experienced rapid response time and significant improvements in time-to-on compared with levodopa.
For more coverage of MDS 2019,
REFERENCE
Rakhimov F, Sultanov B. Management of akinesia in Parkinson’s disease with apomorphine subcutaneous injection. Presented at: MDS 2019. September 22-26, 2019. Abstract 184.
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