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Completed Phase 2 Interventional Results available

PT003 MDI Dose Confirmation Study

ClinicalTrials.gov ID: NCT01349816

Public ClinicalTrials.gov record NCT01349816. 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 Jul 23, 2026, 6:21 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 Randomized, Double Blind, Chronic Dosing (7 Days), Two Period, Six Treatment, Incomplete Block, Cross Over, Multi Center Study to Assess Efficacy and Safety of Four Doses of PT003 MDI in Patients With Moderate to Severe COPD, Compared With Its Individual Components (PT005 MDI and PT001 MDI) as Active Controls

Study identification

NCT ID
NCT01349816
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pearl Therapeutics, Inc.
Industry
Enrollment
185 participants

Conditions and interventions

Interventions

  • PT003 Drug
  • PT001 Drug
  • PT005 Drug

Drug

Eligibility (public fields only)

Age range
40 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
May 31, 2011
Primary completion
Oct 31, 2011
Completion
Oct 31, 2011
Last update posted
Apr 26, 2017

2011

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Pearl Investigative Site Rancho Mirage California
Pearl Investigative Site Colorado Springs Colorado
Pearl Investigative Site Waterbury Connecticut
Pearl Investigative Site Clearwater Florida
Pearl Investigative Site Pensacola Florida
Pearl Investigative Site Stockbridge Georgia
Pearl Investigative Site Minneapolis Minnesota
Pearl Investigative Site Brooklyn New York
Pearl Investigative Site Charlotte North Carolina
Pearl Investigative Site Winston-Salem North Carolina
Pearl Investigative Site Cincinnati Ohio
Pearl Investigative Site Medford Oregon
Pearl Investigative Site Spartanburg South Carolina

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01349816, 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 Apr 26, 2017 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01349816 live on ClinicalTrials.gov.

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