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FDA grants extended approval for Trisenox to treat acute promyelocytic leukemia

Read time: 1 mins
Last updated: 23rd Jan 2018
Published: 23rd Jan 2018
Source: Pharmawand

Teva Pharmaceutical Industries Ltd. announced that the FDA has approved the use of Trisenox (arsenic trioxide) injection in combination with tretinoin for the treatment of adults with newly-diagnosed low-risk acute promyelocytic leukemia (APL) whose APL is characterized by the presence of the t(15;17) translocation or PML/RAR-alpha gene expression.

 

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