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Sponsors and Collaborators: |
National Center for Research Resources (NCRR) University of Michigan |
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Information provided by: | Office of Rare Diseases (ORD) |
ClinicalTrials.gov Identifier: | NCT00004643 |
OBJECTIVES: I. Evaluate the toxicity of cytarabine in patients with refractory systemic lupus erythematosus.
II. Evaluate objective disease parameters, including serum complement levels, anti-DNA antibody titers, sedimentation rate, and the systemic lupus activity measure in these patients.
Condition | Intervention | Phase |
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Lupus Erythematosus, Systemic |
Drug: cytarabine |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Open Label |
Ages Eligible for Study: | 18 Years to 64 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
PROTOCOL ENTRY CRITERIA:
Disease Characteristics
Prior/Concurrent Therapy
Patient Characteristics
Study ID Numbers: | 199/11685, UMMC-91208 |
Study First Received: | February 24, 2000 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00004643 |
Health Authority: | United States: Federal Government |
arthritis & connective tissue diseases immunologic disorders and infectious disorders rare disease systemic lupus erythematosus |
Autoimmune Diseases Lupus Erythematosus, Systemic Arthritis |
Rare Diseases Connective Tissue Diseases Cytarabine |
Antimetabolites Anti-Infective Agents Antimetabolites, Antineoplastic Immunologic Factors Molecular Mechanisms of Pharmacological Action Immune System Diseases |
Antineoplastic Agents Therapeutic Uses Physiological Effects of Drugs Immunosuppressive Agents Antiviral Agents Pharmacologic Actions |