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OpenTrials
Completed

NCT Number: NCT00053976

Methylprednisolone With or Without Daclizumab in Treating Patients With Acute Graft-Versus-Host Disease

The purpose of this study is to compare the effects of IL2 receptor antibody (also known as Daclizumab or Zenapax) and corticosteroids alone for control of GVHD. Treatment with corticosteroids is standard care for GVHD. This research is being done because the investigators do not know whether addition of this new medication to standard corticosteroid therapy improves response rates. Since Zenapax binds to a type of cell which is thought to cause GVHD and possibly inactivates them, investigators have reason to believe that addition of Zenapax night result in better control of GVHD This study will determine whether the addition of another medication, Zenapax, will be more effective than steroids alone in suppressing GVHD and improving symptoms of GVHD.

Daclizumab (Zenapax) is approved by the Food and Drug Administration (FDA) for use in patient with kidney transplant to help prevent graft rejection. This medication has been used in bone marrow transplant patients to treat GVHD.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Brigham and Women's Hospital, Boston, Massachusetts, United States

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About this study

GVHD occurs when the donor's immune system recognizes a patient's body as foreign and reacts against it. GVHD may result in skin rashes and blistering, liver inflammation and gastrointestinal problems including nausea, vomiting, diarrhea and bleeding. Mild GVHD may be treated with topical medications applied to the skin. More severe GVHD requires medications given intravenously (by vein) or taken by mouth. Steroids are usually given first to treat GVHD but only 40% of people respond to this alone.

OBJECTIVES:

  • Compare response to treatment in patients with acute graft-versus-host disease (GVHD) treated with methylprednisolone with or without daclizumab.
  • Compare differences in total methylprednisolone dose and complications in patients treated with these regimens.
  • Compare mortality, days of antibiotics and antifungal therapy, and required hospital days within the first 100 days for patients treated with these regimens.
  • Compare overall survival and incidence of chronic GVHD at 1 year in patients treated with these regimens.

OUTLINE: This is a randomized, placebo-controlled, double-blind, multicenter study. Patients are stratified according to prior graft-versus-host disease (GVHD) prophylaxis (immunosuppressive therapy vs T-cell depletion), GVHD organ manifestation (skin only vs other), donor type (6/6 matched sibling vs other), and participating center. Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive methylprednisolone or equivalent corticosteroid IV or orally and daclizumab IV over 15 minutes on days 0, 3, 7, 14, and then weekly as indicated until day 100.
  • Arm II: Patients receive methylprednisolone or equivalent corticosteroid as in arm I and placebo.

Patients are followed at 1 year and then annually thereafter.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Allogeneic Transplantation
  • Acute GVHD requiring therapy (skin stage 2 or overall grade II-IV)
  • Signed, informed consent

Exclusion criteria

  • Mental or emotional contraindications as determined by patient's physician
  • Steroids given prophylactically or therapeutically at a dose > 1 mg/kg/d methylprednisolone (including prevention of acute GVHD or treatment for diffuse alveolar hemorrhage and severe obstructive mucositis within 7 days prior to starting acute GVHD therapy. Steroids administered as amphotericin premedication are allowed if below 1 mg/kg/day.
  • Acute GVHD diagnosed solely by virtue of upper GI GVHD
  • Hypersensitivity to Daclizumab or prior therapy with Daclizumab
  • GVHD from donor lymphocyte infusion
  • Other investigational therapeutics within 30 days of enrollment
  • Pregnancy or of fertile, failure to agree to use contraception

Treatment and study plan

Daclizumab

Biological

Other names: Zenapax

methylprednisolone

Drug

Placebo

Drug

Primary outcomes

  1. Rate of decrease of acute GVHD grade

    Time frame: Day 42

Secondary outcomes

  1. 100 Day Mortality

    Time frame: 100 Day

  2. Complete Response of GVHD

    Time frame: 100 Days

  3. Total Days of Antibiotic or Antifungal

    Time frame: 100 Days

  4. Number of Hospitalized Days

    Time frame: 100 Days

  5. Total Steroid Dose

    Time frame: 100 Days

  6. Number of Participants with Steroid related Complication

    Time frame: 1 Year

  7. Overall Survival

    Time frame: 100 Days

  8. Relapse Rate

    Time frame: 1 Years

Sponsors and collaborators

Lead sponsor

Dana-Farber Cancer Institute

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Treatment of Acute Graft vs. Host Disease With Steroids Plus Daclizumab (Zenapax) or Placebo

Important dates

Study start
2001
Primary completion
2003
Study completion
2004
First posted
Feb 6, 2003
Registry last updated
Jan 23, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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