A 24-week treatment, multi-center, randomized, double-blind, double-dummy, parallel group study to compare Umeclidinium/Vilanterol, Umeclidinium, and Salmeterol in subjects with chronic obstructive pulmonary disease (COPD)

  • STATUS
    Recruiting
  • sponsor
    GlaxoSmithKline
Updated on 25 March 2021

Summary

A 24-week treatment, multi-center, randomized, double-blind, double-dummy, parallel group study to compare Umeclidinium/Vilanterol, Umeclidinium, and Salmeterol in subjects with chronic obstructive pulmonary disease (COPD)

Description

This study is basically comparing two products that are already on the market for patients with COPD, which includes chronic bronchitis and emphysema. The study lasts for approximately 6 months and compensation is provided for your time and travel. Compensation is provided for your time and travel expenses.

Details
Clinical Study IdentifierTX147799
SponsorGlaxoSmithKline
Last Modified on25 March 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Must be 40 years of age or older
Must have been a previous or a current smoker for a minimum of 10 pack-years, which means an average of one pack a day for 10 years
Cannot have a diagnosis of Asthma to be eligible for this study
There are several medication restrictions so it's important to let us know what medications you are currently taking
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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