Long-term safety, tolerability and efficacy of aclidinium bromide in Patients with moderate to severe Chronic Obstructive Pulmonary Disease (COPD) (LAS-MD-35) - LAS-MD-35

Study identifier:LAS-MD-35

ClinicalTrials.gov identifier:NCT01044459

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Long-Term, Randomized, Double-Blind Study of the Safety, Tolerability and Efficacy of Aclidinium Bromide At Two Dosage Levels When Administered to Patients With Moderate to Severe, Stable Chronic Obstructive Pulmonary Disease

Medical condition

Chronic Obstructive Pulmonary Disease

Phase

Phase 3

Healthy volunteers

No

Study drug

Aclidinium Bromide 200 µg, Aclidinium Bromide 400 µg

Sex

All

Actual Enrollment

605

Study type

Interventional

Age

40 Years +

Date

Study Start Date: 01 Nov 2009
Primary Completion Date: 01 Apr 2011
Study Completion Date: 01 Apr 2011

Study design

Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment

Verification:

Verified 01 Feb 2017 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria