Teva Secures European Approval of Trisenox for First Line Treatment of Low to Intermediate Risk Acute Promyelocytic Leukemia » FINCHANNEL
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Teva Receives FDA Priority Review for First Line Use of TRISENOX® (arsenic trioxide) in Patients with Low to Intermediate Risk Acute Promyelocytic Leukemia (APL) | media
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Fresenius Kabi Introduces Leukemia Drug Arsenic Trioxide Injection in 10 mg per 10 mL vial - Fresenius Kabi USA
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EC approves Teva's Acute Promyelocytic Leukaemia drug
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EU approval of Teva's Trisenox® for first line treatment of low to intermediate risk APL - Hospital Pharmacy EuropeHospital Pharmacy Europe
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How a drug for few patients was turned into $81 million in sales | Pharma's Windfall | The Seattle Times
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Teva Secures European Approval of Trisenox for First Line Treatment of Low to Intermediate Risk Acute Promyelocytic Leukemia » FINCHANNEL
Teva's Trisenox Gets FDA Approval as First-Line Treatment
Teva Negotiating Sale of Remaining Women's Health Assets, Report Says | Ctech
