Study of Muromonab-CD3 and Cyclosporine in Patients With Giant Cell Myocarditis
Primary Purpose
Myocarditis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Muromonab-CD3
Cyclosporine
Sponsored by
About this trial
This is an interventional treatment trial for Myocarditis focused on measuring Giant Cell Myocarditis
Eligibility Criteria
Inclusion criteria: Idiopathic heart failure and/or arrhythmia of less than 3 months duration Endomyocardial biopsy diagnostic of idiopathic giant cell myocarditis Negative pregnancy test Exclusion criteria: Clinical evidence of sepsis or active infection (e.g., meningitis or osteomyelitis) Pregnant Any contraindication to immunosuppression Allergy to cyclosporine or muromonab-CD3 Creatinine greater than 2.5 mg/dL AST or ALT greater than 3 times upper limit of normal Other severe concurrent disease that would preclude study Unreliable or uncooperative subject
Sites / Locations
- Mayo Clinic Rochester
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00027443
Brief Title
Study of Muromonab-CD3 and Cyclosporine in Patients With Giant Cell Myocarditis
Official Title
Giant Cell Myocarditis Treatment Trial Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2001
Overall Recruitment Status
Completed
Study Start Date
August 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2007 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Mayo Clinic
4. Oversight
5. Study Description
Brief Summary
This is a study to determine the efficacy of muromonab-CD3 and cyclosporine as treatment in patients with giant cell myocarditis (GCM). T lymphocytes appear to be involved in GCM. Muromonab-CD3 has been shown to reduce the number of lymphocytes and cyclosporine inhibits lymphocyte activation. This treatment may prolong patient survival until transplantation or ventricular assist device placement is possible.
Detailed Description
Each patient will be randomized to receive either standard care and immunosuppression therapy (treatment group) or standard care alone (control group). To prevent bias, randomization will be stratified by recency of symptom onset to ensure that both the treatment and control groups are balanced with respect to it. Within each of these 2 strata, permuted-block randomization will be done to keep the number of treatment and control patients balanced. Due to the necessary monitoring of the patients randomized to receive immunosuppression therapy, treatment cannot be blinded. Approximately 1 year after the last patient has been randomized, the observed times from randomization to the composite endpoint (death, transplantation, or LVD placement) will be compared in the treatment and control groups.
Completion date provided represents the completion date of the grant per OOPD records
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocarditis
Keywords
Giant Cell Myocarditis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Muromonab-CD3
Intervention Type
Drug
Intervention Name(s)
Cyclosporine
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Idiopathic heart failure and/or arrhythmia of less than 3 months duration
Endomyocardial biopsy diagnostic of idiopathic giant cell myocarditis
Negative pregnancy test
Exclusion criteria:
Clinical evidence of sepsis or active infection (e.g., meningitis or osteomyelitis)
Pregnant
Any contraindication to immunosuppression
Allergy to cyclosporine or muromonab-CD3
Creatinine greater than 2.5 mg/dL
AST or ALT greater than 3 times upper limit of normal
Other severe concurrent disease that would preclude study
Unreliable or uncooperative subject
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leslie T Cooper, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic Rochester
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
19026310
Citation
Cooper LT Jr, Hare JM, Tazelaar HD, Edwards WD, Starling RC, Deng MC, Menon S, Mullen GM, Jaski B, Bailey KR, Cunningham MW, Dec GW; Giant Cell Myocarditis Treatment Trial Investigators. Usefulness of immunosuppression for giant cell myocarditis. Am J Cardiol. 2008 Dec 1;102(11):1535-9. doi: 10.1016/j.amjcard.2008.07.041. Epub 2008 Sep 18.
Results Reference
derived
Learn more about this trial
Study of Muromonab-CD3 and Cyclosporine in Patients With Giant Cell Myocarditis
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