Arcus Biosciences reported collaboration and license revenues of $26.8 million for the second quarter ended June 30, 2022, and a net loss of $66.6 million. The company's cash, cash equivalents, and investments totaled $1.27 billion, expected to fund operations into 2026. They are advancing clinical programs, including four registrational Phase 3 trials with domvanalimab-based combinations.
Four registrational Phase 3 trials evaluating domvanalimab-based combinations are ongoing or expected to start by year-end.
An interim analysis was conducted for the ongoing Phase 1/1b ARC-8 trial of quemliclustat plus chemotherapy, with or without zimberelimab, in pancreatic ductal adenocarcinoma (PDAC).
Arcus is on track to initiate ARC-20, a Phase 1/1b study to evaluate AB521, Arcus’s HIF-2a inhibitor, in cancer patients in Q3 2022.
Arcus nominated a new development candidate, AB801 (an AXL inhibitor), in the second quarter; and at least two new molecules are expected to advance into the clinic in 2023.
Arcus Biosciences anticipates several milestones in their clinical programs. Topline disclosure from the Phase 2 ARC-7 study and data from the randomized cohort of ARC-6 are expected in the second half of 2022. Data from ARC-9 are expected in the first half of 2023.
Analyze how earnings announcements historically affect stock price performance