Efficacy and Safety Trial of RPC1063 for Moderate to Severe Crohn's Disease

Overview

About this study

The purpose of this study is to determine the effectiveness of RPC1063 in the initial treatment of moderate to severely active Crohn's disease.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria

  • Crohn's disease confirmed by endoscopy and histology
  • Active disease as evaluated by Crohn's Disease Activity Index Score and Simple Endoscopic Score for CD
  • Inadequate response to aminosalicylates, corticosteroids, immunomodulators or biologic therapy

Exclusion Criteria

  • Diagnosis of ulcerative colitis or indeterminate colitis
  • Known strictures/stenosis leading to symptoms of obstruction
  • Current stoma or need for ileostomy or colostomy
  • Clinically relevant cardiovascular conditions or other relevant diseases that could impact the implementation or interpretation of the trial, or put the patient at risk
  • History of uveitis or known macular edema
  • History of colonic dysplasia

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Edward Loftus, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available
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CLS-20169985

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