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).
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.
Condition | Autoimmune Thrombocytopenic Purpura |
---|---|
Treatment | Doxil |
Clinical Study Identifier | NCT00107913 |
Sponsor | Hematology and Oncology Specialists |
Last Modified on | 22 January 2022 |
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