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Completed Phase 2 Interventional Results available

A Phase 2 Study of MP-376 to Prevent Acute Exacerbations in Chronic Obstructive Pulmonary Disease (COPD) Patients

ClinicalTrials.gov ID: NCT00739648

Public ClinicalTrials.gov record NCT00739648. 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 Jun 26, 2026, 11:50 AM EDT

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

Official title

Phase 2, Randomized, Double-Blind, Placebo-Controlled, Study to Evaluate the Safety, Tolerability and Efficacy of MP-376 Inhalation Solution Administered for 5 Days Every 28 Days to Prevent Acute Exacerbations in High Risk COPD Patients

Study identification

NCT ID
NCT00739648
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Amgen
Industry
Enrollment
322 participants

Conditions and interventions

Interventions

  • MP-376 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 Years and older
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
Sep 30, 2008
Primary completion
Dec 31, 2009
Completion
Mar 31, 2010
Last update posted
Dec 26, 2024

2008 – 2010

United States locations

U.S. sites
39
U.S. states
17
U.S. cities
39
Facility City State ZIP Site status
Not listed Haleyville Alabama 35565
Not listed Hueytown Alabama 35023
Not listed Mobile Alabama 36608
Not listed Montgomery Alabama 36117
Not listed Glendale Arizona 85306
Not listed Phoenix Arizona 85006
Not listed Chula Vista California 91911
Not listed Lomita California 90717
Not listed Long Beach California 90822
Not listed Mission Viejo California 92691
Not listed Oceanside California 92056
Not listed Palo Alto California 94304
Not listed Riverside California 92506
Not listed San Diego California 92117
Not listed San Jose California 95124
Not listed Wheat Ridge Colorado 80033
Not listed Clearwater Florida 33765
Not listed DeBary Florida 32713
Not listed DeLand Florida 32720
Not listed Orlando Florida 32806
Not listed Savannah Georgia 31406
Not listed New Orleans Louisiana 70115
Not listed Taylor Michigan 48180
Not listed Omaha Nebraska 68198
Not listed Buffalo New York 14215
Not listed Ithaca New York 14850
Not listed Greenville North Carolina 27834
Not listed Columbus Ohio 43210
Not listed Maumee Ohio 43537
Not listed Toledo Ohio 43614
Not listed Medford Oregon 97504
Not listed Johnston Rhode Island 02919
Not listed Easley South Carolina 29640
Not listed Gaffney South Carolina 29340
Not listed Spartanburg South Carolina 29303
Not listed Union South Carolina 29379
Not listed San Antonio Texas 78212
Not listed Richmond Virginia 23225
Not listed Salem Virginia 24153

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 NCT00739648, 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 Dec 26, 2024 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00739648 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →