Mechanism of Action: Volasertib (BI 6727)
Volasertib (BI 6727) is a potent and selective inhibitor of PLK1 in vitro that is currently being evaluated for its therapeutic potential to target the cell cycle.
Volasertib (BI 6727) is a potent and selective inhibitor of PLK1 in vitro that is currently being evaluated for its therapeutic potential to target the cell cycle. Volasertib selectively binds to the ATP binding pocket of PLK1, thereby inhibiting its ability to regulate cell division, and resulting in cell cycle arrest.
The FDA has granted a Breakthrough Therapy designation to volasertib in combination with low-dose cytarabine (LDAC) for its potential as a treatment for patients with untreated acute myeloid leukemia (AML) who are ineligible for intensive remission induction therapy.
Read more on the Breakthrough Therapy designation >>
Epcoritamab Delivers Durable Responses in Anthracycline-Ineligible LBCL
December 12th 2024Fixed-duration, subcutaneous epcoritamab-bysp achieved durable responses with a manageable safety profile in older patients with newly diagnosed large B-cell lymphoma who are not candidates for anthracycline-based therapy.
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