Drug news

FDA grants extended approval for Trisenox to treat acute promyelocytic leukemia

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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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