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NCT03733561 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess Pharmacokinetic Profiles of LY03003 and Neupro

A Phase 1 study of Parkinson Disease, sponsored by Luye Pharma Group.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target
1
Study location

NCT03733561: Completed Phase 1 study of Parkinson Disease, sponsored by Luye Pharma Group.

NCT03733561 is a Phase 1 study of Parkinson Disease that has completed, run by Luye Pharma Group. The registered enrollment target is 40 participants, below the 5,326-participant average among 297 other Parkinson Disease trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03733561, a Phase 1 study of Parkinson Disease, has completed, sponsored by Luye Pharma Group.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

Phase 1, single center study to assess pharmacokinetic profiles of rotigotine after single dose of LY03003 and daily patch application of Neupro in Healthy Volunteers

Conditions Studied

Interventions

  • DRUG LY03003
  • DRUG Neupro 4Mg/24Hr Transdermal Patch

Study Locations (1)

Maryland

  • Pharmaron CPC, Inc. - Baltimore

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2018-11-09
Est. Completion 2018-12-23
Phase Phase 1
Luye Pharma Group

22 total trials

What the finished NCT03733561 record still lists

NCT03733561 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 5,326-participant average among 297 other Parkinson Disease trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Parkinson Disease appearing as the primary indexed condition, and to 2 interventions - of which LY03003 is the first listed.

NCT03733561 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT03733561 about?

NCT03733561 is a clinical study titled "A Study to Assess Pharmacokinetic Profiles of LY03003 and Neupro". Phase 1, single center study to assess pharmacokinetic profiles of rotigotine after single dose of LY03003 and daily patch application of Neupro in Healthy Volunteers

What is the current status of trial NCT03733561?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2018-11-09. Estimated completion is 2018-12-23.

What conditions does trial NCT03733561 study?

This clinical trial studies the following conditions: Parkinson Disease.

What interventions are being tested in trial NCT03733561?

The interventions under investigation include: LY03003 (DRUG), Neupro 4Mg/24Hr Transdermal Patch (DRUG).

Who is sponsoring clinical trial NCT03733561?

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

Where is trial NCT03733561 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Parkinson Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03733561's enrollment target sits among peer trials

40 173rd of 297 higher than 109 of 297 other Parkinson Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Parkinson Disease 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 NCT03733561, the US trial registry maintained by the National Library of Medicine. NCT03733561 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.