An Efficacy and Safety Study of Sirukumab in Participants With Major Depressive Disorder

  • STATUS
    Recruiting
  • sponsor
    Janssen Research &
Updated on 23 November 2020

Summary

An Efficacy and Safety Study of Sirukumab in Participants With Major Depressive Disorder

Description

The purpose of this study is to evaluate the efficacy of sirukumab as adjunctive treatment to antidepressant therapy, where sirukumab is measured over a 12 week study period for treatment of depression symptoms.

Qualified participants receive study-related medical care and study medication or placebo at no cost and may be compensated for time and travel.

Details
Clinical Study IdentifierTX145916
SponsorJanssen Research &
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Ages Eligible for Study: 21 Years to 64 Years (Adult)
Genders Eligible for Study: Both
Participant is diagnosed with Major Depressive Disorder
Patient must be located within 60 miles of CNS study location
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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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