Efficacy, Safety, and Tolerability of aclidinium bromide in the treatment of moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD) (LAS-MD-38) - LAS-MD-38

Study identifier:LAS-MD-38

ClinicalTrials.gov identifier:NCT01045161

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Tolerability of 2 Doses of Aclidinium Bromide Compared With Placebo for 12 Weeks in Patients with Moderate to Severe, Stable Chronic Obstructive Pulmonary Disease Followed by a 40-Week Evaluation of the higher Aclidinium Bromide Dose

Medical condition

Chronic Obstructive Pulmonary Disease

Phase

Phase 3

Healthy volunteers

No

Study drug

Aclidinium bromide, Placebo

Sex

All

Actual Enrollment

544

Study type

Interventional

Age

40 Years +

Date

Study Start Date: 01 Mar 2009
Primary Completion Date: 01 Jun 2011
Study Completion Date: 01 Jun 2011

Study design

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

Verification:

Verified 01 Nov 2016 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria