Ankylosing Spondylitis Study

  • STATUS
    Recruiting
Updated on 23 November 2020

Summary

It’s Time to Stand Up to Ankylosing Spondylitis!

Take Part in Research of an Oral Investigational Medication for Ankylosing Spondylitis

If you are still suffering from the pain and stiffness of ankylosing spondylitis (AS) symptoms despite treatment, you may want to consider participating in a research study of an oral investigational medication for AS.

 

Description

For qualified study participants, all investigational medication (or inactive placebo), study-related tests and study doctor visits will be provided at no cost to you for the duration of the study. You may also be reimbursed for any out-of-pocket expenses required for you to attend study visits.

Details
Condition Ankylosing Spondylitis, Ankylosing spondylitis
Clinical Study IdentifierTX227282
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

You may qualify if you
Are a male or female, at least 18 years old
Have received a diagnosis of AS Are currently experiencing AS symptoms
Have tried other medications to treat AS that either didn’t work or you stopped using because of side effects
Are willing to follow a plan of study visits, laboratory tests, and other study procedures for the duration of the study, approximately 56 weeks
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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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