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RCUS

Arcus Biosciences, Inc.NYSEHealthcare
$22.96+5.13%ClosedMarket Cap: $2.31B

As of 2026-04-06

Valuation

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P/E (TTM)

PEG

P/B

3.79

P/S

9.06

EV/EBITDA

-6.72

DCF Value

$-39.27

FCF Yield

-21.6%

Div Yield

0.0%

Margins & Returns

Gross Margin

98.0%

Operating Margin

-156.3%

Net Margin

-142.9%

ROE

-65.8%

ROA

-31.0%

ROIC

-42.5%

Financials

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PeriodRevenueNet IncomeEPS
Q4 2025$33.0M$-98.0M$-0.92
FY 2025$247.0M$-353.0M$-3.29
Q3 2025$26.0M$-135.0M$-1.27
Q2 2025$160.0M$-8.0M$0.04

Analyst Ratings

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WedbushOutperform
2026-04-02
CitigroupBuy
2026-03-05
HC Wainwright & Co.Buy
2026-03-02
Leerink PartnersOutperform
2026-03-02
Wells FargoEqual Weight
2026-02-12

Trading Activity

Insider Trades

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Markus Richardofficer: Chief Medical Officer
SellMon Jan 26
Markus Richardofficer: Chief Medical Officer
SellMon Jan 26
ROSEN TERRY Jdirector, officer: Chief Executive Officer
SellMon Jan 26
ROSEN TERRY Jdirector, officer: Chief Executive Officer
SellMon Jan 26
Jaen Juan C.officer: President
SellMon Jan 26

Company Info

Sector

Healthcare

Industry

Country

US

Exchange

NYSE

Beta

0.86

Arcus Biosciences, Inc., a clinical-stage biopharmaceutical company, develops and commercializes cancer therapies in the United States. Its product pipeline includes, Etrumadenant, a dual A2a/A2b adenosine receptor antagonist, which is in a Phase 1b/2 clinical trial; and Zimberelimab, an anti-PD-1 antibody that is in Phase 1b clinical trial for monotherapy. The company also develops Domvanalimab, an anti-TIGIT monoclonal antibody, which is in Phase 2 development for the treatment of first-line metastatic non-small cell lung cancer in combination with Zimberelimab; Quemliclustat, a small-molecule CD73 inhibitor is in a Phase 1/1b study for the treatment of first-line metastatic pancreatic cancer; and AB521, an oral and small molecule HIF-2a inhibitor that is in Phase 1 study for the treatment of patients with von Hippel- Lindau disease. It has a clinical development collaboration agreement with Strata Oncology, Inc. to evaluate Zimberelimab; a collaboration with AstraZeneca, BVF Partners L.P to evaluate domvanalimab, its investigational anti-TIGIT antibody, in combination with Imfinzi (durvalumab) in a registrational Phase 3 clinical trial in patients with unresectable Stage III non-small cell lung cancer; and license agreements with Taiho Pharmaceutical Co., Ltd, Abmuno Therapeutics LLC, and WuXi Biologics to develop anti-CD39 antibody for the treatment of cancer. The company was incorporated in 2015 and is headquartered in Hayward, California.

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