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Arcus Biosciences(RCUS) - 2025 Q1 - Quarterly Report

Revenue Generation - The company has not generated any revenue from product sales and does not expect to do so for the foreseeable future, with all revenue recognized to date coming from research, collaboration, and license arrangements [145]. - Total revenues for the three months ended March 31, 2025, decreased to 28million,down8128 million, down 81% from 145 million in the same period of 2024 [156]. - License and development services revenue fell to 20million,adecreaseof8520 million, a decrease of 85% compared to 135 million in the prior year [156]. Clinical Programs - The company has seven clinical programs targeting unique indications, including HIF-2α, TIGIT, and PD-1, with significant collaboration agreements in place with Gilead [137]. - The median progression-free survival (mPFS) for the 50mg twice-a-day casdatifan monotherapy cohort reached 9.7 months, with confirmed objective response rates ranging from 25% to 33% [149]. - Most patients (81-87%) experienced disease control with either a partial response or stable disease while on treatment [143]. - The company retains full global development and commercial rights for the HIF-2α program after Gilead's option rights expired [141]. - The company is not pursuing a Phase 3 study for etrumadenant at this time, despite promising results from the ARC-9 study [144]. Financial Performance - Research and development expenses increased by 12% to 122millionforthethreemonthsendedMarch31,2025,upfrom122 million for the three months ended March 31, 2025, up from 109 million in 2024 [158]. - Early-stage R&D and preclinical program expenses surged by 68% to 42million,comparedto42 million, compared to 25 million in the previous year [158]. - Net cash used in operating activities was 132millionforthethreemonthsendedMarch31,2025,comparedto132 million for the three months ended March 31, 2025, compared to 2 million in the same period of 2024 [171]. - General and administrative expenses are expected to remain stable for the remainder of the year [153]. Funding and Cash Position - In February 2025, the company issued 13.6 million shares at 11.00pershare,resultingintotalgrossproceedsofapproximately11.00 per share, resulting in total gross proceeds of approximately 150 million [141]. - Cash provided by financing activities amounted to 142million,primarilyfromtheissuanceofcommonstockinFebruary2025[173].AsofMarch31,2025,thecompanyhad142 million, primarily from the issuance of common stock in February 2025 [173]. - As of March 31, 2025, the company had 210 million in deferred revenue related to performance obligations with Gilead [178]. - The company has a term loan facility of 250million,with250 million, with 50 million drawn at closing and an additional $100 million available [168]. - Gilead acquired approximately 29.7% of the company's outstanding common stock as of March 31, 2025, following a stock purchase agreement [166]. - The company believes its cash and investments will be sufficient to fund operations for at least twelve months following the report date [164]. Future Expectations - The company expects R&D expenses to peak in 2025 and then decline significantly as programs advance towards regulatory approval [151]. - The company anticipates significant growth in development capabilities and infrastructure as it advances clinical-stage programs [151].