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NCT02807675 · ClinicalTrials.gov registry record · Phase 1

A Study of the Safety and Tolerability of a Single Dose Administration of CVT-301 (Levodopa Inhalation Powder)

A Phase 1 study of Parkinson's Disease, sponsored by Acorda Therapeutics.

Completed
Registry status
Phase 1
Development phase
36
Enrollment target
11
Study locations

NCT02807675 is a Phase 1 study of Parkinson's Disease that has completed, run by Acorda Therapeutics. The registered enrollment target is 36 participants, below the 639-participant average among 157 other Parkinson's Disease trials with a reported enrollment target (94% lower). The trial reports 11 study locations across 6 states.

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The verdict

NCT02807675, a Phase 1 study of Parkinson's Disease, has completed, sponsored by Acorda Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
36 participants
Enrollment target
11
Study locations

Study Summary

This study is a double-blind, randomized, placebo-controlled, 2-way crossover study to evaluate the safety of CVT-301 levodopa (l-dopa) when co- administered with the first daily dose of oral levodopa/carbidopa for early morning OFF symptoms in patients with Parkinson's disease (PD).

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG CVT-301, LIP

Study Locations (11)

Florida

  • Site #9002 - Boca Raton
  • Site #9017 - Hallandale
  • Site #9008 - St. Petersburg
  • Site #9018 - Sunrise
  • Site #9004 - Tampa

Michigan

  • Site #9003 - Farmington Hills
  • Site #9005 - West Bloomfield

California

  • Site #9015 - Fountain Valley

Georgia

  • Site #9016 - Atlanta

Illinois

  • Site #9009 - Chicago

Tennessee

  • Site #9007 - Nashville

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2016-06
Est. Completion 2016-11
Phase Phase 1

Sponsor

Acorda Therapeutics

36 total trials

What the Registry Record Tells You About NCT02807675

The ClinicalTrials.gov registry entry for NCT02807675 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 639-participant average among 157 other Parkinson's Disease trials with a reported enrollment target (94% lower). The listed sponsor is Acorda Therapeutics, which has 36 total studies on file at ClinicalTrials.gov.

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

NCT02807675 reports 11 study locations spanning 6 distinct geographic areas - top geographies include Florida, Michigan, California.

Frequently Asked Questions

What is clinical trial NCT02807675 about?

NCT02807675 is a clinical study titled "A Study of the Safety and Tolerability of a Single Dose Administration of CVT-301 (Levodopa Inhalation Powder)". This study is a double-blind, randomized, placebo-controlled, 2-way crossover study to evaluate the safety of CVT-301 levodopa (l-dopa) when co- administered with the first daily dose of oral levodopa/carbidopa for early morning OFF symptoms in patients with Parkinson's disease (PD).

What is the current status of trial NCT02807675?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2016-06. Estimated completion is 2016-11.

What conditions does trial NCT02807675 study?

This clinical trial studies the following conditions: Parkinson's Disease.

What interventions are being tested in trial NCT02807675?

The interventions under investigation include: Placebo (OTHER), CVT-301, LIP (DRUG).

Who is sponsoring clinical trial NCT02807675?

This trial is sponsored by Acorda Therapeutics, which has 36 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02807675 being conducted?

This trial has 11 study locations across California, Florida, Georgia, Illinois, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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