Expired Study
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Metairie, Louisiana 70006


Purpose:

This study is designed to evaluate the efficacy and safety of single agent Doxil in the treatment of patients with refractory ITP (Idiopathic Thrombocytopenic Purpura).


Study summary:

Eligible patients will receive Doxil 20 mg/m2 IV over 1 hour every 2 weeks. Treatment will be continued for 1 course beyond return of the platelet count to normal with a maximum of 18 courses.


Criteria:

Inclusion Criteria: - Thrombocytopenia with bone marrow findings showing normal or increased numbers of megakaryocytes. - Failure to respond to initial treatment with steroids, IV immune globulin, splenectomy and post splenectomy steroids. - Platelet count of 30,000 or less. - Performance status score of 2 or less. - Adequate organ function: *bilirubin< 2; *AST < 3 times normal; *creatinine < 2. - No prior treatment with anthracycline or chemically related drugs. Exclusion Criteria: - Pregnant or lactating women. - Presence of a malignancy other than basal cell carcinoma of the skin.


NCT ID:

NCT00107913


Primary Contact:

Principal Investigator
Thomas M Cosgriff, MD
Hematology and Oncology Specialists


Backup Contact:

N/A


Location Contact:

Metairie, Louisiana 70006
United States

Mary Ann Ostroske, RN
Phone: 504-894-7115
Email: mostroske1@salco.net

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: December 16, 2017

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