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Therapeutic Areas: Gastroenterology | Immunology | Family Medicine
Disease Category: Ulcerative Colitis
Location: United States, VA

Clinical Trial Details

Overview

Research Study Summary

A Phase 2/3 Multicenter, Randomized, Placebo-controlled, Double-blind Study to Evaluate the Safety and Efficacy of XXXXXXXXX Induction Therapy, Administered Subcutaneously, in Subjects with Moderately to Severely Active Ulcerative Colitis.

Purpose

A Phase 2/3 Multicenter, Randomized, Placebo-controlled, Double-blind Study to Evaluate the Safety and Efficacy of XXXXXXXXX Induction Therapy, Administered Subcutaneously, in Subjects with Moderately to Severely Active Ulcerative Colitis.

Patient Inclusion Criteria:

  • Male or female at least 18 years of age

Patient Exclusion Criteria:

  • History of tuberculosis (TB)
  • History of HIV, Hepatitis B or Hepatitis C
  • History of cancer within the past 5 years (exception: non-melanoma skin cancer)
  • History of Congestive Heart Failure

To Learn more
Phase

2/3

Gender

Both Male and Female

Age

18 and up

Overall Status

Recruiting

Facility Type

N/A

Contact

Michelle Spady, Research Manager
Gastroenterology Associates of Tidewater
112 Gainsborough Square, Suite 200
Chesapeake, VA 23320
Phone: 757-547-0798 ext. 1134
Fax: 757-410-4123

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Research Center Information: Gastroenterology Associates of Tidewater

If you would like to learn more about participating in this research study, please email the trial contact using the form below.

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CW ID: 152596

Date Last Changed: July 24, 2013


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