Are you an adult between the ages of 18 - 75 with asthma? Help us study investigational therapies for this disease.

  • STATUS
    Recruiting
Updated on 25 January 2021
asthma
asthmatic
allergic asthma
asthma attack
bronchial asthma

Summary

We are looking for adults with asthma to participate in a clinical research study. Strict infection control measures are taken at all study sites to minimize the potential risk of exposure to COVID-19 while participating.

Description

Qualified participants receive either the test product (Fluticasone Propionate), the FDA approved drug (Flovent HFA), or Placebo to be taken daily for a period of 4 weeks.

Details
Condition Asthma, Allergies & Asthma, Asthma (Pediatric), Allergy
Clinical Study IdentifierTX261018
Last Modified on25 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age between 18 yrs and 75 yrs?
Gender: Male or Female
Do you have any of these conditions: Asthma (Pediatric) or Allergies & Asthma or Allergy or Asthma?
Are between 18 - 75 years of age
Have a diagnosis of asthma at least 6 months prior to enrollment
Are stable on your asthma treatment regimen for at least 4 weeks prior to enrollment
Are currently not smoking (including non-tobacco products)
Able to comply with study procedures, including correct use of inhaler devices and home peak expiratory flow (PEF) device, and maintaining an electronic diary (eDiary)
Are willing to give your written informed consent to participate
Additional eligibility criteria may apply

Exclusion Criteria

Contact Site for Exclusion Criteria
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How to participate?

Step 1 Connect with a site
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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