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Completed Phase 2 Interventional

Study To Evaluate The Efficacy And Safety Of PH-797804 For 12 Weeks In Adults With Moderate To Severe Chronic Obstructive Pulmonary Disease (COPD) Taking Salmeterol Xinafoate/Fluticasone Propionate Combination

ClinicalTrials.gov ID: NCT01321463

Public ClinicalTrials.gov record NCT01321463. 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, 8:42 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 II, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study To Evaluate The Efficacy And Safety Of Once-Daily Orally Administered PH-797804 For 12 Weeks In Adults With Moderate To Severe Chronic Obstructive Pulmonary Disease (COPD) On A Background Of Salmeterol Xinafoate/ Fluticasone Propionate Combination

Study identification

NCT ID
NCT01321463
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
377 participants

Conditions and interventions

Interventions

  • PH-797804 Drug
  • Placebo 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
Apr 30, 2011
Primary completion
May 31, 2012
Completion
May 31, 2012
Last update posted
Jul 10, 2013

2011 – 2012

United States locations

U.S. sites
22
U.S. states
12
U.S. cities
20
Facility City State ZIP Site status
Pfizer Investigational Site Mobile Alabama 36608
Pfizer Investigational Site Glendale Arizona 85306
Pfizer Investigational Site San Diego California 92120
Pfizer Investigational Site Clearwater Florida 33756
Pfizer Investigational Site Pensacola Florida 32504
Pfizer Investigational Site Tampa Florida 33603
Pfizer Investigational Site Tampa Florida 33613
Pfizer Investigational Site Trinity Florida 34655
Pfizer Investigational Site Conyers Georgia 30094
Pfizer Investigational Site Duluth Georgia 30096
Pfizer Investigational Site Norcross Georgia 30071
Pfizer Investigational Site Livonia Michigan 48152
Pfizer Investigational Site Fridley Minnesota 55432
Pfizer Investigational Site Minneapolis Minnesota 55407
Pfizer Investigational Site Rochester Minnesota 55905
Pfizer Investigational Site St Louis Missouri 63141
Pfizer Investigational Site Cincinnati Ohio 45231
Pfizer Investigational Site Cincinnati Ohio 45245
Pfizer Investigational Site Lincoln Rhode Island 02865
Pfizer Investigational Site Spartanburg South Carolina 29303
Pfizer Investigational Site Houston Texas 77030
Pfizer Investigational Site McKinney Texas 75069

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 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01321463, 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 Jul 10, 2013 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01321463 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →