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June 11, 2014
08:38 EDTCPXXCelator announces data, recommendation to continue CPX-351 Phase 3 study
Celator Pharmaceuticals announced that the independent Data and Safety Monitoring Board for the Company's Phase 3 clinical study of CPX-351 Liposome Injection versus the conventional cytarabine and daunorubicin treatment regimen as first-line therapy in older patients with high-risk acute myeloid leukemia has completed a planned safety review and recommended that the study should continue as planned without any modifications. The primary efficacy endpoint of the study is overall survival. The study is being conducted in the U.S. and Canada, with more than 40 leading cancer centers participating.
News For CPXX From The Last 14 Days
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June 29, 2015
08:09 EDTCPXXCelator Pharmaceuticals announces LLS accelerates payment for CPX-351 study
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June 24, 2015
09:10 EDTCPXXOn The Fly: Pre-market Movers
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08:08 EDTCPXXCelator Pharmaceuticals to host conference call
Conference call to discuss positive induction response results from phase 3 study of CPX-351 will be held on June 24 at 8:30 am. Webcast Link
07:04 EDTCPXXCelator Pharmaceuticals' Acute Myeloid Leukemia candidate shows positive results
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June 19, 2015
10:00 EDTCPXXOn The Fly: Analyst Initiation Summary
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08:24 EDTCPXXCelator Pharmaceuticals initiated with a Buy at MLV & Co.
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