[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

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Study’s contact

Call center

+1 855-218-9153

Email address

ct.gov@arenapharm.com

Condition

Ulcerative Colitis

Treatment type

Interventional

Investigational product

Etrasimod

Phase

Phase 2

Sponsor

Pfizer

ClinicalTrials.gov identifier

NCT05287126

Study number

APD334-207

Understanding clinical trials

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About the study

The purpose of this study is to determine the safety, efficacy, and pharmacokinetics (PK) of etrasimod for the treatment of moderately to severely active ulcerative colitis in adolescents (≥ 12 years up to < 18 years of age). Participants who will complete the total 52-week treatment period will have the opportunity to continue in a Long-Term Extension (LTE) Period of up to 4 years (5 years after study enrollment), or until marketing authorization is obtained in the participant's country, whichever comes first.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria

  1. Have a diagnosis of ulcerative colitis (UC) that is moderately to severely active
  2. Participants are permitted to be receiving a therapeutic dose of select UC therapies
Exclusion criteria

  1. Severe extensive colitis
  2. Diagnosis of Crohn's disease (CD) or indeterminate colitis or the presence or history of a fistula consistent with CD
  3. Diagnosis of microscopic colitis, ischemic colitis, or infectious colitis

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

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