Study ID

SLMF4010

Clinical Study ID

SLMF 4010

Study Title Multicentre, randomised, parallel group, placebo-controlled, double-blind, study, stratified on tobacco status at enrollment, evaluating during 6 months the efficacy of salmeterol powder for inhalation, 50 μg two times per day for the reduction of thoracic distension in subjects with chronic obstructive pulmonary disease (COPD)
Clinicaltrials.gov Identifier
Sponsor GlaxoSmithKline
Collaborators N/A
Phase phase 4
Study Recruitment Status Completed
Generic Name salmeterol
Trade Name serevent
Study Indication Pulmonary Disease, Chronic Obstructive

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GSK-sponsored clinical studies are those for which GSK is ultimately responsible for all aspects of the study even if some or all of these activities are transferred to another party.
GSK-sponsored clinical trials are those for which GSK is ultimately responsible for all aspects of the study even if some or all of these activities are transferred to another party.

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