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Myfortic - Treatment for Extensive cGvHD

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00298324
Recruitment Status : Terminated (Due to slow accrual)
First Posted : March 2, 2006
Last Update Posted : April 3, 2015
Information provided by:
European Group for Blood and Marrow Transplantation

Brief Summary:
The purpose of this study is to determine whether the response to treatment for extensive chronic Graft versus Host Disease (cGvHD)is improved with the addition of myfortic alongside cyclosporine A and prednisone, compared to the reference treatment of cyclosporine A and prednisone alone.

Condition or disease Intervention/treatment Phase
Graft vs Host Disease Drug: Myfortic Drug: Prednisone and Cyclosporine Phase 3

Detailed Description:

This clinical trial is a European, multi-center, randomized, double blinded placebo-controlled trial comparing CsA+PDN+MPA versus the reference treatment of CsA+PDN alone + placebo, in patients with extensive chronic GvHD. Randomization will be stratified according to:

  • Platelet number (low versus high risk)
  • Source of transplantable cells (marrow versus PBSC versus cord blood)

Patients not in progression at 6 weeks post randomization (progression defined as primary failure) will be evaluated for remission (complete or partial) at 3, 6, 9, & 12 months post randomization

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 34 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: A Randomized Double Blinded Placebo-Controlled Phase III Trial Comparing Cyclosporine Plus Steroids With or Without Myfortic as Primary Treatment for Extensive Chronic Graft Versus Host Disease
Study Start Date : September 2006
Actual Primary Completion Date : November 2009
Actual Study Completion Date : November 2010

Arm Intervention/treatment
Active Comparator: Myfortic
Patients in this arm will receive Myfortic + Prednisone + Cyclosporine
Drug: Myfortic
1440mg twice daily

Standard Care/ Placebo
In this arm patients will receive Prednisone + Cyclosporine + Placebo or Prednisone + Cyclosporine
Drug: Prednisone and Cyclosporine
Prednisone and Cyclosporine given according to protocol. The drugs are tapered according to patient response

Primary Outcome Measures :
  1. To test whether the addition of Myfortic improves the efficacy of prednisone plus cyclosporine for treatment of newly diagnosed chronic GvHD, as defined by the proportion of patients with efficacy success at 1 year after enrollment. [ Time Frame: 1 year ]

Secondary Outcome Measures :
  1. The hazard rates of efficacy success between the two arms. Loss of donor chimerism or recurrent malignancy before secondary systemic therapy and before discontinuation of all immunosuppressive meds will be treated as competing risks. [ Time Frame: 1 year ]
  2. efficacy failure, and treatment failure defined as efficacy failure or premature discontinuation of study-drug administration due to toxicity [ Time Frame: 1 year ]
  3. survival without recurrent malignancy [ Time Frame: 1 year ]
  4. Overall survival [ Time Frame: 1 year ]
  5. cumulative incidence of secondary systemic treatment for cGvHD before recurrent malignancy [ Time Frame: 1 year ]
  6. the cumulative incidence of death without recurrent or malignancy [ Time Frame: 1 year ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Age 18 - 60
  • Any primary diagnosis requiring treatment by hematopoietic stem cell transplantation
  • Recipient of a single allogeneic stem cell transplant (bone marrow or peripheral blood stem cells, or cord blood) minimum 80 days ago
  • Received a graft from a related or an unrelated donor
  • Conditioning regimen: Myeloablative or non-myeloablative
  • Patients suffering a first episode of extensive chronic GvHD, without recurrent disease
  • The diagnosis of chronic GvHD requires the following:

    • Distinction from acute GvHD
    • Presence of at least one diagnostic clinical sign of chronic GvHD or presence of at least one distinctive sign confirmed by pertinent biopsy or other relevant diagnostic tests
    • Exclusion of other possible diagnoses
  • Receiving a standard prophylaxis regimen for acute GvHD: CsA plus methotrexate, or CSA+MMF for NMA, or a T-cell depleted transplant
  • Patient gives written informed consent prior to randomization

Exclusion Criteria:

  • Patient age less than 18 years or over 60 years.
  • GvHD prophylaxis by tacrolimus plus methotrexate
  • Delayed onset acute GvHD following NMA or DLI
  • Second allogeneic stem cell transplant
  • Not the first episode of chronic GvHD needing systemic immunosuppressive therapy.
  • Limited chronic GvHD (Seattle criteria, see Appendix 1)
  • Uncontrolled systemic infection which in the opinion of the investigator is associated with an increased risk of the patient's death within 1 week of randomization
  • In the opinion of the investigator, if the patient has significant medical or psychosocial problems or unstable disease status
  • Pregnant or lactating females
  • Known hypersensitivity to mycophenolic acid

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00298324

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Hopital St. Louis
Paris, France, 75475
University Regensburg
Regensburg, Germany, 93042
Ospedale San Martino
Genova, Italy, 16132
University Hospital
Maastricht, Netherlands, 6202
Hospital Clínico Universitario
Valencia, Spain, 46010
Karolinska University Hospital
Huddinge, Sweden, 141 86
University Hospital
Basel, Switzerland, 4031
University Faculty of Medicine
Ankara, Turkey, 06260
Sponsors and Collaborators
European Group for Blood and Marrow Transplantation
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Study Chair: Gérard Socié Hôptial St Louis, Paris

Additional Information:
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Responsible Party: Ruzena Uddin, EBMT Identifier: NCT00298324     History of Changes
Other Study ID Numbers: EudraCT 2005-006178-86
First Posted: March 2, 2006    Key Record Dates
Last Update Posted: April 3, 2015
Last Verified: April 2015
Keywords provided by European Group for Blood and Marrow Transplantation:
graft versus host disease
Additional relevant MeSH terms:
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Mycophenolic Acid
Graft vs Host Disease
Immune System Diseases
Anti-Inflammatory Agents
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Immunosuppressive Agents
Immunologic Factors
Antifungal Agents
Anti-Infective Agents
Dermatologic Agents
Antirheumatic Agents
Calcineurin Inhibitors
Antibiotics, Antineoplastic
Antibiotics, Antitubercular
Antitubercular Agents
Anti-Bacterial Agents