Apokyn for Motor IMProvement of Morning AKinesia Trial (AM IMPAKT) (AM IMPAKT)
A Phase 4, Open-Label, Efficacy and Safety Study of Apokyn® for Rapid and Reliable Improvement of Motor Symptoms in Parkinson Disease Subjects With Delayed Onset of L-Dopa Action
Sponsor: MDD US Operations, LLC a subsidiary of Supernus Pharmaceuticals
A PHASE4 clinical study on Akinesia and Delayed Levodopa Onset, this trial is completed. The trial is conducted by MDD US Operations, LLC a subsidiary of Supernus Pharmaceuticals and has accumulated 12 data snapshots since 2012. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
12 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE4
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Sep 2024 — Sep 2025 [monthly]
Completed PHASE4
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Jul 2024 — Sep 2024 [monthly]
Completed PHASE4
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Sep 2023 — Jul 2024 [monthly]
Completed PHASE4
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Mar 2022 — Sep 2023 [monthly]
Completed PHASE4
▶ Show 7 earlier versions
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Dec 2021 — Mar 2022 [monthly]
Completed PHASE4
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Jan 2021 — Dec 2021 [monthly]
Completed PHASE4
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Jun 2018 — Jan 2021 [monthly]
Completed PHASE4
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Dec 2017 — Jun 2018 [monthly]
Completed PHASE4
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Jun 2017 — Dec 2017 [monthly]
Completed PHASE4
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Feb 2017 — Jun 2017 [monthly]
Completed PHASE4
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE4
First recorded
Dec 2012
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- MDD US Operations, LLC a subsidiary of Supernus Pharmaceuticals
For direct contact, visit the study record on ClinicalTrials.gov .