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Completed Phase 2 Interventional

Efficacy and Safety Study of Inhaled CVT 301 in Parkinson's Disease Patients for Treatment of OFF Episodes

ClinicalTrials.gov ID: NCT01777555

Public ClinicalTrials.gov record NCT01777555. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 1:45 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Randomized, Double-blind, Placebo-controlled Study Investigating the Efficacy and Safety of Inhaled CVT 301 (Levodopa Inhalation Powder) in Parkinson's Disease Patients With Motor Response Fluctuations (OFF Phenomena)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized, multicenter, placebo-controlled, double-blind study will evaluate the efficacy and safety of inhaled CVT 301 compared with placebo in PD patients experiencing motor response fluctuations (OFF phenomena) as an outpatient (i.e., at home) and in the clinic.

Study identification

NCT ID
NCT01777555
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Acorda Therapeutics
Industry
Enrollment
89 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
30 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2013
Primary completion
Dec 31, 2013
Completion
Dec 31, 2013
Last update posted
Aug 7, 2018

2013 – 2014

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
13
Facility City State ZIP Site status
Civitas Investigational Site 1013 Little Rock Arkansas 72201
Civitas Investigational Site 1004 Boca Raton Florida 33427
Civitas Investigational Site 1002 Port Charlotte Florida 33948
Civitas Investigational Site 1015 Tampa Florida 33601
Civitas Investigational Site 1007 Kansas City Kansas 66101
Civitas Investigational Site 1010 Boston Massachusetts 02108
Civitas Investigational Site 1001 Bingham Farms Michigan 48025
Civitas Investigational Site 1008 Roseville Michigan 48066
Civitas Investigational Site 1009 Saint Louis Michigan 48880
Civitas Investigational Site 1005 West Bloomfield Michigan 48322
Civitas Investigational Site 1011 Kingston New York 12401
Civitas Investigational Site 1014 Cleveland Ohio 44101
Civitas Investigational Site 1003 Kirkland Washington 98033

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01777555, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 7, 2018 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01777555 live on ClinicalTrials.gov.

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