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NCT02728947 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetic Profile of Neupro Patch Administrated at 2 mg, 4 mg, 6 mg and 8 mg/Day Weekly in Patients With Early-stage Parkinson's Disease

A Phase 1 study, sponsored by Luye Pharma Group.

Completed
Registry status
Phase 1
Development phase
28
Enrollment target

NCT02728947: Completed Phase 1 study, sponsored by Luye Pharma Group.

NCT02728947 is a Phase 1 study that has completed, run by Luye Pharma Group. The registered enrollment target is 28 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02728947, a Phase 1 study, has completed, sponsored by Luye Pharma Group.

COMPLETED
Registry status
Phase 1
Development phase
28 participants
Enrollment target

Study Summary

To study the profile of Neupro patch administrated at 2 mg, 4 mg, 6 mg and 8 mg/day weekly in patients with early-stage Parkinson's disease

Primary Outcome

PK parameters Cmax-ss

Interventions

  • DRUG ROTIGOTINE

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2016-05
Est. Completion 2016-09
Phase Phase 1
Luye Pharma Group

22 total trials

What the finished NCT02728947 record still lists

NCT02728947 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% lower).

The record links to 0 conditions, and to 1 intervention - of which ROTIGOTINE is the first listed.

NCT02728947 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02728947 about?

NCT02728947 is a clinical study titled "Pharmacokinetic Profile of Neupro Patch Administrated at 2 mg, 4 mg, 6 mg and 8 mg/Day Weekly in Patients With Early-stage Parkinson's Disease". To study the profile of Neupro patch administrated at 2 mg, 4 mg, 6 mg and 8 mg/day weekly in patients with early-stage Parkinson's disease

What is the current status of trial NCT02728947?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2016-05. Estimated completion is 2016-09.

What interventions are being tested in trial NCT02728947?

The interventions under investigation include: ROTIGOTINE (DRUG).

Who is sponsoring clinical trial NCT02728947?

This trial is sponsored by Luye Pharma Group, which has 22 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02728947's enrollment target sits among peer trials

28 1447th of 2000 higher than 538 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02728947, the US trial registry maintained by the National Library of Medicine. NCT02728947 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.