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Current Studies - Takayasu's Arteritis (TAK) and Giant Cell (Temporal) Arteritis (GCA) Studies

5523: Concurrent Pilot Studies in Giant Cell Arteritis and Takayasu’s Arteritis to Examine the Safety, Efficacy, and Immunologic Effects of Abatacept (CTLA4-Ig) in Large Vessel Vasculitis (AGATA)

Status: Recruiting

Summary:

Please Note: The Rare Diseases Clinical Research Network will make every effort to enroll all the patients we can, but we cannot make any guarantees that we will be able to enroll everyone in a particular study who wants to participate.

Background

Giant cell arteritis (GCA) and Takayasu's arteritis (TAK) are types of vasculitis that affect large arteries and may involve vessels that supply blood to different parts of the body including the brain, eyes, arms, legs, lungs, kidneys, intestines, heart, and other parts. The purpose of this study is to determine if the medication abatacept is safe and effective in giant cell arteritis or Takayasu's arteritis.

About this Study

In the beginning of this study, all subjects will receive abatacept (by vein) combined with standard doses of prednisone. If there is no sign of GCA or TAK at month 3, you will be assigned by chance (like flipping a coin) to continue abatacept or switch to a placebo (fake treatment or inactive look-a-like) for the rest of the study. Your total time on the study will range from 12 to 48 months (1-4 years). About 66 people will take part in this study (33 with GCA and 33 with TAK) across 4 medical centers. You will be examined by the following:

  • Medical history review
  • Physical exam
  • Imaging (x-rays, MRI)
  • Blood/urine tests
  • Lung function tests
  • Study questionnaires
  • Skin test

Target Enrollment:

To be eligible to participate, you must:

  1. have a diagnosis of GCA or TAK
  2. have presence of GCA or TAK within the past 2 months
  3. be 15 years of age or older
  4. be willing and able to follow treatment and follow-up procedures
  5. be willing to use an effective means of birth control during this study
  6. be willing and able to give written informed consent

You are not eligible to participate if:

  1. you have signs of an infection
  2. you are pregnant or breast feeding
  3. you are infected with HIV, hepatitis C, or hepatitis B
  4. you are not able to follow study guidelines
  5. you are not able to give informed consent
  6. you have a reduced number of blood cells
  7. you have a poor kidney(s)

How to Participate:

In order to participate in a study, you must personally contact the study coordinator of any of the participating institutions by phone or by e-mail. Please use the information below to inquire about participation.

United States

Canada

California

  • Cedars-Sinai Medical Center, Los Angeles
    Nadia Verde
    Study Coordinator
    Phone: 310-360-9197
    E-mail: nadia.verde@cshs.org

Massachusetts

  • Boston University School of Medicine, Boston
    Daniel Finkel
    Study Coordinator
    E-mail: dfinkel@bu.edu
    Phone: 617-414-2509

Minnesota

  • Mayo Clinic College of Medicine, Rochester
    Jane Jaquith
    Study Coordinator
    E-mail: jaquith.jane@mayo.edu
    Phone: 507-284-4502

New York

  • Hospital for Special Surgery, New York
    Morgana Davids
    Research Assistant
    E-mail: davidsm@hss.edu
    Phone: 212-774-2123

Ohio

  • Cleveland Clinic Foundation, Cleveland
    Katherine Tuthill
    Study Coordinator
    E-mail: tuthillk@ccf.org
    Phone: 216-444-5257

Pennsylvania

  • University of Pennsylvania, Philadelphia
    Leah Madden
    Study Coordinator
    E-mail: Leah.Madden@uphs.upenn.edu
    Phone: 215-614-4406

  • University of Pittsburgh, Pittsburgh
    Dawn McBride, RN, BA
    Study Coordinator
    E-mail: dlmc@pitt.edu
    Phone: 412-586-3545

Utah

Ontario

  • St. Joseph's Healthcare, Hamilton
    Sandra Messier, RCT
    Vascular Medicine Research Coordinator
    E-mail: smessier@stjoes.ca
    Phone: 905-522-1155 Ext. 35873

  • University of Toronto Mount Sinai Hospital, Toronto
    Julia Farquharson
    Study Coordinator
    E-mail: jfarquharson@mtsinai.on.ca
    Phone: 416-586-8616

Join the Contact Registry for: Takayasu's Arteritis (TAK) | Giant Cell (Temporal) Arteritis (GCA)

Download Study Flyer for: Concurrent Pilot Studies in Giant Cell Arteritis and Takayasu’s Arteritis to Examine the Safety, Efficacy, and Immunologic Effects of Abatacept (CTLA4-Ig) in Large Vessel Vasculitis (AGATA) [PDF]

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