Arcus Biosciences reported fourth-quarter financial results, highlighting a cash balance of $735.1 million and an additional $220.4 million received from Gilead after year-end. The company is advancing its pipeline, including registrational trials for domvanalimab and multiple data readouts expected in 2021.
Gilead increased its ownership in Arcus from approximately 13.0% to 19.5%.
Arcus initiated ARC-10, its first registrational trial, evaluating domvanalimab + zimberelimab vs. zimberelimab vs. chemotherapy in first-line PD-L1≥50%, locally advanced or metastatic NSCLC.
Promising preliminary data from the dose-escalation portion of ARC-8, evaluating AB680 in combination with zimberelimab and gemcitabine/nab-paclitaxel in first-line metastatic pancreatic cancer, were presented at ASCO GI in January.
Arcus received IND clearance for AB308, Arcus’s FcR-enabled anti-TIGIT antibody, in January.
Arcus Biosciences anticipates multiple key data read-outs in 2021, including the ARC-7 interim analysis in Q2 2021. The company expects to continue advancing AB680 in pancreatic cancer and expand its clinical program to other tumor types. Arcus also plans to advance at least one new small molecule program into clinical development in the second half of 2021.
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