Decisions and readouts loom for the SERDs Astra’s camizestrant and Roche’s giredestrant.
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But biomarker enrichment and toxicity remain key for FX-909.
The month saw the first commissioner's priority voucher approval in oncology.
The first fruit of a long-standing deal with Roche enters phase 1 in March.
An FDA verdict is due in the third quarter, as Protagonist looks likely to opt out.
Welireg looks headed to regulators in second-line and adjuvant kidney cancer.
The company will license EGFR and cMet inhibitors from Celyn.
The combo gets another slam dunk, this time in perioperative chemo-eligible MIBC.
