Arcus Biosciences

Arcus Biosciences (RCUS) Q4 2025 Earnings

Reported Feb 25, 2026 at 4:08 PM ET · SEC Source

Q4 25 EPS

$-0.89

BEAT +11.59%

Est. $-1.01

Q4 25 Revenue

$33.0M

BEAT +25.00%

Est. $26.4M

vs S&P Since Q4 25

+33.1%

BEATING MARKET

RCUS +42.7% vs S&P +9.5%

Full Year 2025 Results

FY 25 EPS

$-3.29

BEAT +6.00%

Est. $-3.50

FY 25 Revenue

$247.0M

BEAT +3.96%

Est. $237.6M

Market Reaction

Did RCUS Beat Earnings? Q4 2025 Results

Arcus Biosciences delivered a stronger-than-expected Q4 2025, beating on both the top and bottom lines as investors focused increasingly on the promise of its lead oncology asset casdatifan. The clinical-stage biotech posted a loss of $0.89 per share… Read more Arcus Biosciences delivered a stronger-than-expected Q4 2025, beating on both the top and bottom lines as investors focused increasingly on the promise of its lead oncology asset casdatifan. The clinical-stage biotech posted a loss of $0.89 per share, ahead of the $1.10 consensus estimate by 19.09%, while revenue of $33.00 million topped the $23.60 million consensus by 39.83% and rose 26.9% year over year. The outperformance was underpinned by the company's deepening late-stage pipeline investments, with R&D spend climbing to $121.00 million in the quarter as Phase 3 studies of casdatifan and quemliclustat advanced. Compelling updated data for casdatifan in clear cell renal cell carcinoma, including a 45.2% confirmed response rate and 15.1-month median progression-free survival, helped send shares sharply higher around the print. Looking ahead, management guided 2026 GAAP revenue of $45.00 million to $55.00 million and expects R&D expenses to decline meaningfully, with cash runway extending at least into the second half of 2028.

Key Takeaways

  • Revenue from Gilead collaboration programs ($23 million in Q4 2025)
  • Taiho option exercise for casdatifan generating $7 million in Q4 2025
  • Gilead pipeline access fees of $3 million in Q4 2025
  • Higher R&D expenses driven by increased enrollment in Phase 3 studies for casdatifan and quemliclustat
  • Lower collaboration reimbursements as Gilead-led activities represented larger share of costs
24/7 Wall St

RCUS YoY Financials

Q4 2025 vs Q4 2024, source: SEC Filings

24/7 Wall St

RCUS Revenue by Segment

With YoY comparisons, source: SEC Filings

Q1 25 Q1 26

“This week's updated data at ASCO GU continue to validate casdatifan's profile as the best-in-class HIF-2a inhibitor and new potential standard-of-care therapy for ccRCC. We are focused on rapidly enrolling PEAK-1, our Phase 3 study evaluating casdatifan plus cabozantinib in IO-experienced patients, as well as determining the optimal TKI-free casdatifan-based regimen for a registrational trial in the 1L setting by the end of the year. Together, the IO-experienced and first line settings represent an over $5 billion peak sales opportunity for casdatifan. We remain extremely well-positioned to execute on our casdatifan program and our emerging inflammation portfolio, with cash runway until at least the second half of 2028.”

— Terry Rosen, Q4 2025 Earnings Press Release