olivlawolivlaw

olivLaw · US equity research

Arcus Biosciences, Inc. RCUS

Pharmaceutical Preparations · SIC 2834 · Vertical: Pharmaceutical Preparations (SIC 2834)

19.31USD+2.12% · 1 dayClose 04 Nov 2026

Arcus Biosciences is a late clinical-stage biopharmaceutical company developing small molecules for cancer and inflammatory and autoimmune diseases. Its most advanced product, casdatifan, is in Phase 3 studies, while the company reported a net loss of 353 million USD in fiscal 2025 and holds 1.0 billion USD to fund its plans.

The AI analysis may be outdated: new filings came after its sources (see the «AI analysis» section).

At the close of 04 Nov 2026, Arcus Biosciences, Inc. (RCUS) stock was 19.31 USD (+2.12% on the day), with market capitalisation 2.8 bn USD, beta 1.47, 52-week range 17.76–31.57 USD. Latest reported quarter (Q3 2026): revenue of 9.0 m USD (−65.4% YoY), net income of -128.0 m USD, diluted EPS -1.00 USD.

Data as of · AI analysis dated · Source: SEC filings and closing prices, computed by olivLaw.

Market cap
2.8 bn USD
shares as of 29 Oct 2026
P/E (TTM)
unavailable
Diluted EPS TTM -3.64 · TTM to 30 Sept 2026
E/P (TTM)
-18.83%
TTM to 30 Sept 2026
Dividend yield
unavailable
Beta (2y)
1.47
Volatility (1y) 62%
52-week range
17.7631.57

Price history

Loading chart…

Technical reading

RSI (14)
39.2
weak (30–45)
Bollinger (20, 2)
15.84 – 25.42
in the lower half of the band · %B 0.36 · band width 46.4%
SMA 50 / 200
24.26 / 24.62
downtrend (price < SMA50 < SMA200)
MACD (12, 26, 9)
-1.76 / -1.82
MACD above signal

Indicators describe past prices; on their own they do not predict direction. On our history the RSI ≤ 40 filter added no return (see the signals methodology).

Performance

CompanyS&P 500vs S&P 500Vertical median
1 month−21.9%−1.1%−20.9 pp—
3 months−30.3%−0.5%−29.8 pp—
6 months−25.7%+4.4%−30.1 pp—
Year to date−19.0%+12.3%−31.3 pp—
1 year−2.6%+13.5%−16.2 pp+8.9%
3 years+18.0%+76.4%−58.5 pp+15.7%
5 years−44.7%+63.7%−108.4 pp—
Max drawdown (1y)
−43.7%
25 Aug 2026 → 26 Oct 2026
Max drawdown (5y)
−85.8%
23 Nov 2021 → 04 Apr 2025
Compound annual growth (5y)
−11.2%
S&P 500 +10.4%

Price returns, dividends excluded.

Quarterly results

Latest quarter: Q3 2026 · 30 Sept 2026

Revenue
9.0 m USD
−65.4% YoY
Net income
-128.0 m USD
unavailable YoY
Diluted EPS
-1.00
unavailable YoY
net / operating
-1,422.2% / -1,455.6%

Quarterly margins

Quarterly statements · USD

Fiscal yearQ4 '24Q1 '25Q2 '25Q3 '25Q4 '25Q1 '26Q2 '26Q3 '26
Revenue26.0 m28.0 m160.0 m26.0 m33.0 m17.0 m41.0 m9.0 m
Research & development101.0 m122.0 m139.0 m141.0 m121.0 m122.0 m113.0 m117.0 m
Operating income-103.0 m-122.0 m-8.0 m-142.0 m-114.0 m-134.0 m-96.0 m-131.0 m
Depreciation & amortisation3.0 m3.0 m2.0 m ≈2.0 m ≈3.0 m2.0 m3.0 m ≈2.0 m ≈
Interest expense2.0 m1.0 m2.0 m3.0 m2.0 m3.0 m3.0 m3.0 m
Pre-tax income-93.0 m-112.0 m0-135.0 m-106.0 m-128.0 m-91.0 m-128.0 m
Income tax1.0 m0000000
Net income-94.0 m-112.0 m0-135.0 m-106.0 m-128.0 m-91.0 m-128.0 m
Diluted EPS-1.03 ≈-1.140.00-1.27-0.90 ≈-1.02-0.72-1.00
Operating cash flow-100.0 m-132.0 m-133.0 m ≈-97.0 m ≈-120.0 m-138.0 m-119.0 m ≈-88.0 m ≈
Capex1.0 m1.0 m0 ≈0 ≈1.0 m00 ≈0 ≈

≈ derived quarter (cumulative difference / share-days average)

E/P over time

E/P = trailing-12-month diluted EPS / price at quarter end. E/P is the inverse of P/E and stays defined when earnings are negative.

Fiscal years

Fiscal year20182019⚠ 20202021⚠ 2022202320242025
Revenue8.4 m15.0 m78.0 m383.0 m112.0 m117.0 m258.0 m247.0 m
Revenue YoY+491.2%+79.6%—+391.0%—+4.5%+120.5%−4.3%
Net income-49.6 m-84.7 m-123.0 m53.0 m-267.0 m-307.0 m-283.0 m-353.0 m
Net income YoYunavailableunavailable—unavailable—unavailableunavailableunavailable
Diluted EPSunavailable-1.93-2.240.71-3.71-4.15-3.14-3.29
Diluted EPS YoYunavailableunavailable—unavailable—unavailableunavailableunavailable
net %-593.7%-564.7%-157.7%13.8%-238.4%-262.4%-109.7%-142.9%
Free cash flow-46.7 m-75.4 m108.0 m-282.0 m432.0 m-330.0 m-176.0 m-484.0 m

The series breaks before 2020, 2022: earlier years come from the original reports of the issuer of that time, later years from a subsequent filing that restated the perimeter (a separation, discontinued operations). The year-on-year change across the break is not shown.

Reported results vs expectations

Loading…

Balance sheet & financial health

Fiscal year 2025 · 31 Dec 2025

Cash
222.0 m USD
Financial debt
99.0 m USD
Net debt
-123.0 m USD
Equity
631.0 m USD
Total assets
1.1 bn USD
Debt / equity
0.16x
Current ratio
4.36x
ROE
-63.3%
ROA
-30.8%
FCF margin
-196.0%

Financial statements (source on every figure)

Revenue and net income (USD)

Margins

Income statement · USD

Revenue
2023
117.0 m
2024
258.0 m
2025
247.0 m

SEC (XBRL)· 25 Feb 2026verified

Research & development
2023
340.0 m
2024
448.0 m
2025
523.0 m

SEC (XBRL)· 25 Feb 2026verified

Operating income
2023
-340.0 m
2024
-330.0 m
2025
-386.0 m

SEC (XBRL)· 25 Feb 2026verified

Depreciation & amortisation
2023
8.0 m
2024
10.0 m
2025
10.0 m

SEC (XBRL)· 25 Feb 2026verified

EBITDA
2023
-332.0 m ≈
2024
-320.0 m ≈
2025
-376.0 m ≈

SEC (XBRL)· 25 Feb 2026derived

Interest expense
2023
2.0 m
2024
4.0 m
2025
8.0 m

SEC (XBRL)· 25 Feb 2026verified

Pre-tax income
2023
-301.0 m
2024
-282.0 m
2025
-353.0 m

SEC (XBRL)· 25 Feb 2026verified

Income tax
2023
6.0 m
2024
1.0 m
2025
0

SEC (XBRL)· 25 Feb 2026verified

Net income
2023
-307.0 m
2024
-283.0 m
2025
-353.0 m

SEC (XBRL)· 25 Feb 2026verified

Diluted EPS
2023
-4.15
2024
-3.14
2025
-3.29

SEC (XBRL)· 25 Feb 2026verified

Weighted average diluted shares
2023
74.0 m
2024
90.1 m
2025
107.4 m

SEC (XBRL)· 25 Feb 2026verified

Balance sheet · USD

Cash
2023
127.0 m
2024
150.0 m
2025
222.0 m

SEC (XBRL)· 25 Feb 2026verified

Current assets
2023
831.0 m
2024
1.0 bn
2025
1.0 bn

SEC (XBRL)· 25 Feb 2026verified

Property, plant & equipment, net
2023
51.0 m
2024
47.0 m
2025
40.0 m

SEC (XBRL)· 25 Feb 2026verified

Total assets
2023
1.1 bn
2024
1.2 bn
2025
1.1 bn

SEC (XBRL)· 25 Feb 2026verified

Accounts payable
2023
17.0 m
2024
18.0 m
2025
42.0 m

SEC (XBRL)· 25 Feb 2026verified

Long-term debt
2023
0
2024
48.0 m
2025
99.0 m

SEC (XBRL)· 25 Feb 2026verified

Current liabilities
2023
184.0 m
2024
226.0 m
2025
231.0 m

SEC (XBRL)· 25 Feb 2026verified

Total liabilities
2023
—
2024
—
2025
—

SEC (XBRL)· 23 Feb 2022verified

Equity
2023
462.0 m †
2024
485.0 m †
2025
631.0 m †

SEC (XBRL)· 25 Feb 2026verified

Cash flow · USD

Operating cash flow
2023
-306.0 m
2024
-170.0 m
2025
-482.0 m

SEC (XBRL)· 25 Feb 2026verified

Capex
2023
24.0 m
2024
6.0 m
2025
2.0 m

SEC (XBRL)· 25 Feb 2026verified

Free cash flow
2023
-330.0 m ≈
2024
-176.0 m ≈
2025
-484.0 m ≈

SEC (XBRL)· 25 Feb 2026derived

Investing cash flow
2023
194.0 m
2024
-84.0 m
2025
66.0 m

SEC (XBRL)· 25 Feb 2026verified

Financing cash flow
2023
33.0 m
2024
277.0 m
2025
488.0 m

SEC (XBRL)· 25 Feb 2026verified

Computed indicators

Growth

Revenue growth (YoY)
-4.3%
computed by olivLawFY 2025
Revenue CAGR 3Y
30.2%
computed by olivLawFY 2022 → FY 2025
Revenue CAGR 5Y
25.9%
computed by olivLawFY 2020 → FY 2025
EBIT growth (YoY)
unavailable
the base of the ratio is not positive
Net income growth (YoY)
unavailable
the base of the ratio is not positive
Net income CAGR 3Y
unavailable
the base of the ratio is not positive
Net income CAGR 5Y
unavailable
the base of the ratio is not positive
EPS growth (YoY)
unavailable
the base of the ratio is not positive
EPS CAGR 3Y
unavailable
the base of the ratio is not positive
EPS CAGR 5Y
unavailable
the base of the ratio is not positive
FCF growth (YoY)
unavailable
the base of the ratio is not positive

Profitability

Gross margin
unavailable
input data missing
EBITDA margin
-465.0%
computed by olivLawTTM to 30 Sept 2026
EBIT margin
-475.0%
computed by olivLawTTM to 30 Sept 2026
Net margin
-453.0%
computed by olivLawTTM to 30 Sept 2026
FCF margin
-466.0%
computed by olivLawTTM to 30 Sept 2026

Returns

ROE
-114.1%
computed by olivLawTTM to 30 Sept 2026 · balance sheet at 30 Sept 2026
ROA
-50.6%
computed by olivLawTTM to 30 Sept 2026 · balance sheet at 30 Sept 2026
ROIC
-131.9%
computed by olivLawTTM to 30 Sept 2026 · balance sheet at 30 Sept 2026
ROCE
-76.7%
computed by olivLawTTM to 30 Sept 2026 · balance sheet at 30 Sept 2026
Payout ratio (EPS)
unavailable
input data missing
Payout ratio (FCF)
unavailable
input data missing

Balance sheet

Net debt
-49.0 m USD
computed by olivLawbalance sheet at 30 Sept 2026
Net debt / EBITDA
unavailable
insufficient data
Debt / equity
0.3x
computed by olivLawbalance sheet at 30 Sept 2026
Interest coverage
-43.2x
computed by olivLawTTM to 30 Sept 2026

Liquidity

Current ratio
3.3x
computed by olivLawbalance sheet at 30 Sept 2026
Quick ratio
unavailable
input data missing
Cash ratio
0.8x
computed by olivLawbalance sheet at 30 Sept 2026

Cash

Operating cash flow
-465.0 m USD
computed by olivLawTTM to 30 Sept 2026
Capital expenditure
1.0 m USD
computed by olivLawTTM to 30 Sept 2026
Free cash flow
-466.0 m USD
computed by olivLawTTM to 30 Sept 2026
FCF conversion
unavailable
insufficient data
Cash conversion
unavailable
insufficient data

Efficiency

Days sales outstanding
unavailable
input data missing
Days inventory outstanding
unavailable
input data missing
Days payables outstanding
unavailable
input data missing
Cash conversion cycle
unavailable
input data missing

Market and valuation

Market capitalisation
2.8 bn USD
computed by olivLawbalance sheet at 30 Sept 2026
Enterprise value
2.7 bn USD
computed by olivLawbalance sheet at 30 Sept 2026
Market cap / net income TTM
unavailable
insufficient data
P/E (TTM)
unavailable
insufficient data
Earnings yield
-18.8%
computed by olivLawTTM to 30 Sept 2026
P/B
7.8x
computed by olivLawbalance sheet at 30 Sept 2026
P/S
27.8x
computed by olivLawTTM to 30 Sept 2026 · balance sheet at 30 Sept 2026
EV/EBITDA
unavailable
insufficient data
EV/EBIT
unavailable
insufficient data
EV/Sales
27.3x
computed by olivLawTTM to 30 Sept 2026 · balance sheet at 30 Sept 2026
P/FCF
unavailable
the base of the ratio is not positive
FCF yield
-16.8%
computed by olivLawTTM to 30 Sept 2026 · balance sheet at 30 Sept 2026
Dividend yield
unavailable
no dividend in the structured statements; a missing line is not a confirmed zero
Shareholder yield (distributions)
unavailable
input data missing

1 indicators that do not apply to the sector.

Valuation

olivLaw classification

Insufficient data
What is missing
  • score weight coverage: 43.8% of at least 60%
  • valuation methods computed: 0 of at least 1

A scoring methodology on indicators and valuation, not investment advice.

Closing price

19.31 USD

04 Nov 2026Source: olivLaw, closing series

Market cap: 2.8 bn USD

Key indicators

Market capitalisation
2.8 bn USD
computed by olivLawbalance sheet at 30 Sept 2026
P/E (TTM)
unavailable
insufficient data
P/B
7.8x
computed by olivLawbalance sheet at 30 Sept 2026
EV/EBITDA
unavailable
insufficient data
ROE
-114.1%
computed by olivLawTTM to 30 Sept 2026 · balance sheet at 30 Sept 2026
Net margin
-453.0%
computed by olivLawTTM to 30 Sept 2026
Revenue growth (YoY)
-4.3%
computed by olivLawFY 2025
Dividend yield
unavailable
no dividend in the structured statements; a missing line is not a confirmed zero

Coverage and freshness

25/37 reporting lines present
Latest full fiscal year: 2025
Latest reported period: 30 Sept 2026
Latest balance sheet date: 30 Sept 2026
Share count (cover of the latest filing), as of: 29 Oct 2026
Source: SEC (XBRL)published 04 Nov 2026
verified 1050derived 86

Score by group

44% · Insufficient data

Estimated value range

unavailable — no valuation method could be computed

Valuation assumptions are editorial choices, not measured; beta is not measured.

Valuation methods

  • DCF (discounted cash flow)unavailable · the base of the ratio is not positive
  • Peers: EV/EBITDAunavailable · the base of the ratio is not positive
  • Peers: P/Eunavailable · the base of the ratio is not positive
  • Dividend discount (DDM)unavailable · the company pays no dividend: a dividend model needs an explicit initiation assumption

no valuation method could be computed

Multiple comparisons use the SIC vertical: Pharmaceutical Preparations (SIC 2834)

Classification (SIC) comparables group by industry code, not by economic activity; the direct group is an editorial selection by activity. Members' multiples are on their own trailing twelve months, at their own latest close.

Assumptions (illustrative, editorial)

Risk-free rate
4.3%
Equity risk premium
5.0%
Beta (default)
1.00
Cost of equity
9.3%
Terminal growth
2.5%

Factor scorecard

Insufficient data

Minimum-evidence gate: score weight coverage: 43.8% of at least 60%; valuation methods computed: 0 of at least 1

FactorValueScoreWeight used
ROIC · Quality-131.9%8 (vs peers)24%
Net margin · Quality-453.0%14 (vs peers)14%
FCF conversion · Qualityunavailableunavailable—
Revenue CAGR 3Y · Growth30.2%100 (on a fixed band)19%
EPS CAGR 3Y · Growthunavailableunavailable—
Net debt / EBITDA · Balance sheetunavailableunavailable—
Interest coverage · Balance sheet-43.2x0 (on a fixed band)14%
Current ratio · Balance sheet3.3x100 (on a fixed band)10%
P/E (TTM) · Valuationunavailableunavailable—
EV/EBITDA · Valuationunavailableunavailable—
FCF yield · Valuation-16.8%0 (on a fixed band)19%
Shareholder yield (distributions) · Returnsunavailableunavailable—
Payout ratio (FCF) · Returnsunavailableunavailable—

Factors without a value were dropped; the remaining weights were renormalised.

Score groups

  • Balance sheet40/100 · 2/3 factors with a value
  • Growth· partial100/100 · 1/2 factors with a value
  • Quality10/100 · 2/3 factors with a value
  • Returns· partialunavailable · 0/2 factors with a value
  • Valuation· partial0/100 · 1/3 factors with a value

A «partial» group is computed from under half of its weight or from one factor: it is not a full assessment of the group.

Memo

Arcus Biosciences, Inc. (RCUS). Latest full fiscal year: 2025; data up to 2026-09-30.

Figures computed from the financial statements: revenue 247.0 m USD in 2025; YoY growth -4.3%; net margin -453.0%; ROE -114.1%.

Valuation cannot be computed from the available data.

Insufficient data for a verdict (score weight coverage: 43.8% of at least 60%; valuation methods computed: 0 of at least 1).

Text generated deterministically from the figures shown; no language model. Not investment advice.

What supports the thesis

  • Revenue CAGR 3Y: 30.2%
  • Current ratio: 3.3x

What contradicts it

  • ROIC: -131.9%
  • Net margin: -453.0%
  • Interest coverage: -43.2x
  • FCF yield: -16.8%

Not assessed (insufficient data or a ratio without meaning): FCF conversion, EPS CAGR 3Y, Net debt / EBITDA, P/E (TTM), EV/EBITDA, Shareholder yield (distributions), Payout ratio (FCF).

Versus the vertical median

Pharmaceutical Preparations (SIC 2834) · same industry (4-digit SIC) · compared with 39 companies

Multiples and returns vs the median

P/E
—
vertical median 38.6x
EV/EBITDA
—
vertical median 20.2x
P/S
27.8x
vertical median 5.5x
above median (+405.4%)
P/B
7.8x
vertical median 4.1x
above median (+88.1%)
ROE
-114.1%
vertical median -6.2%
below median
Net margin
-453.0%
vertical median 9.7%
below median (−4,747.5%)
EBIT margin
-475.0%
vertical median 10.2%
below median (−4,740.4%)
Revenue YoY
-4.3%
vertical median 5.4%
below median (−179.5%)
Net debt/EBITDA
—
vertical median -0.2x
Dividend yield
—
vertical median 2.2%

Price rebased to 100 (monthly, 5 years)

Companies in the vertical

Market capP/EROENet marginRevenue YoY1A / 3A
LLYEli Lilly And Company1,334.0 bn46.086.1%31.9%+44.7%+32% / +140%
JNJJohnson & Johnson665.2 bn41.920.0%16.2%+6.0%+34% / +79%
ONCBeone Medicines Ltd.558.4 bn869.914.7%10.7%+40.2%+11% / +102%
ABBVAbbVie Inc.521.1 bn50.7—15.7%+8.6%+29% / +107%
MRKMerck & Co., Inc.370.7 bn154.75.1%3.6%+1.3%+43% / +47%
ABTAbbott Laboratories200.1 bn43.09.2%9.7%+5.7%−10% / +11%
PFEPfizer Inc175.5 bn43.94.4%6.3%−1.6%+20% / +1%
VRTXVertex Pharmaceuticals Inc139.2 bn35.320.8%30.7%+8.9%+27% / +55%
BMYBristol-Myers Squibb Company131.2 bn14.244.1%18.5%−0.2%+30% / +30%
TEVATeva Pharmaceutical Industries Limited48.8 bn97.46.6%3.6%+4.3%+56% / +326%
ZTSZoetis Inc.36.9 bn14.764.4%27.5%+2.3%−30% / −50%
ROIVRoivant Sciences Ltd.27.6 bn—-6.2%-3,535.0%−71.6%+84% / +300%
RPRXRoyalty Pharma plc26.2 bn47.76.9%25.7%+5.1%+69% / +150%
UTHRUnited Therapeutics Corporation25.9 bn23.019.1%38.6%+10.6%+25% / +154%
INSMInsmed Inc24.1 bn—-72.5%-39.9%+66.7%−47% / +340%
VTRSViatris Inc.22.1 bn—-23.6%-23.9%−3.0%+80% / +109%
ALNYAlnylam Pharmaceuticals, Inc.21.6 bn8.1126.6%52.8%+65.2%−64% / −4%
ORKAOruka Therapeutics, Inc.6.7 bn—-18.2%—unavailable+237% / +364%
RCUSArcus Biosciences, Inc.2.8 bn—-114.1%-453.0%−4.3%−3% / +18%
HRMYHarmony Biosciences Holdings, Inc.2.0 bn11.418.7%18.1%+21.5%−2% / +18%
OMEROmeros Corp1.3 bn10.5——−34.0%+88% / +730%
VSTMVerastem, Inc.892.0 m—-471.2%-231.6%+209.1%−7% / +43%
COLLCollegium Pharmaceutical, Inc.770.6 m19.117.6%5.9%+23.6%−49% / −8%
IBOImpact BioMedical, INC.442.1 m560.3371.3%2,254.3%unavailable−27% / unavailable
KMDAKamada Ltd428.0 m21.27.6%11.2%+12.1%+11% / +57%

1- and 3-year price returns: for RCUS from daily closes (the same as the performance table), for the other companies from month-end closes.

olivLaw engine forecast

The world engine ran after the company's latest material disclosure. Probabilities are of TOUCHING a level within the horizon (not closing there) and sit next to the random walk (p_rw), the no-information benchmark.

The engine has no published run for this company yet.

Valuation scenarios (editable assumptions)

Illustrative scenarios

Illustrative: not forecasts and without probabilities. Each case is one coherent set of assumptions, computed on today's figures.

Bear
Allowed range: -50 … 50%
Allowed range: -100 … 100%
Allowed range: 0 … 100
Allowed range: -10 … 20%
Allowed range: 0 … 100%
Base
Allowed range: -50 … 50%
Allowed range: -100 … 100%
Allowed range: 0 … 100
Allowed range: -10 … 20%
Allowed range: 0 … 100%
Bull
Allowed range: -50 … 50%
Allowed range: -100 … 100%
Allowed range: 0 … 100
Allowed range: -10 … 20%
Allowed range: 0 … 100%
Nothing is saved.

Estimated price (USD)

Estimated priceBearBaseBull
1 years
insufficient data
Total return unavailable · Per year unavailable
insufficient data
Total return unavailable · Per year unavailable
insufficient data
Total return unavailable · Per year unavailable
3 years
insufficient data
Total return unavailable · Per year unavailable
insufficient data
Total return unavailable · Per year unavailable
insufficient data
Total return unavailable · Per year unavailable
5 years
insufficient data
Total return unavailable · Per year unavailable
insufficient data
Total return unavailable · Per year unavailable
insufficient data
Total return unavailable · Per year unavailable
What moves the 3-year price the most

    AI analysis

    AI-generatedAI-generated analysis (Claude) from cited public sources; it may contain errors. Not investment advice. As of 27 Oct 2026 · Model: claude-haiku-5-5.

    Possibly outdated: the newest document it read is from 05 Aug 2026; since then the company filed 8-K (04 Nov 2026 · results), 10-Q (04 Nov 2026), 8-K (21 Oct 2026 · results).

    In brief

    Arcus Biosciences is a late clinical-stage biopharmaceutical company developing small molecules for cancer and inflammatory and autoimmune diseases. Its most advanced product, casdatifan, is in Phase 3 studies, while the company reported a net loss of 353 million USD 1 in fiscal 2025 and holds 1.0 billion USD 1 to fund its plans.

    SWOT

    Strengths

    • The company has a portfolio of small molecules in advanced clinical stages and an oncology program with favourable comparative data against belzutifan 1.
    • Partnerships with several large companies provide financial support and access to diverse therapeutic combinations 12.
    • The company solely owns casdatifan outside the territories licensed to Taiho, which keeps control over its main program 1.

    Weaknesses

    • The company has no approved products and no product sales revenue, which makes its reliance on external funding very high 1.
    • Repeated net losses and a growing accumulated deficit raise questions about its ability to become profitable over the long term 1.
    • Several important programs, including anti-TIGIT studies, were stopped for futility, showing the fragility of the portfolio 12.

    Opportunities

    • If the PEAK-1 and TKI-free studies confirm casdatifan's efficacy, the company could access large oncology markets 1.
    • Oral inflammation programs could open a new growth phase if the first candidate enters the clinic in 2026 1.
    • New collaborations for casdatifan with several partners could widen the range of indications and combinations tested 2.

    Threats

    • Negative study results, as with anti-TIGIT, could reduce the value of several programs at once 2.
    • Competition in renal oncology and anti-inflammatory therapies is intense, and competitors with approved products have a clear advantage 1.
    • Safety risks, such as the immune-mediated events seen in the volrustomig study, could delay or halt important programs 1.

    Risks

    • No product revenuehigh

      The company has no approved products and does not expect product sales revenue for the foreseeable future, which depends on clinical success and regulatory approvals 1.

    • Need for additional fundinghigh

      If the company cannot raise capital when needed, it could be forced to reduce or stop development programs 1.

    • Restrictions in the loan agreementmedium

      The Hercules agreement limits debt, investments and dividends, and an event of default could accelerate repayment 1.

    • Clinical trial failureshigh

      Stopping studies for lack of efficacy shows results can be negative, and the remaining programs could meet the same fate 2.

    • Dependence on partnersmedium

      Gilead and Taiho hold important rights to programs, and changes in their decisions could alter timelines and project value 12.

    Investment thesis

    What would need to be true (bull case)

    • If the PEAK-1 study confirms casdatifan's advantages over belzutifan, the company could hold an important position in renal cancer treatment 1.
    • Recent collaborations with several partners could expand testing of casdatifan and bring resources without fully diluting the company's control 2.
    • If the first inflammation candidate enters the clinic, the program could open a new growth direction beyond oncology 1.

    What would break the thesis

    • The company has no approved products and continuing net losses could force new share issuances or programme cuts 1.
    • The discontinuation of several anti-TIGIT studies shows results can disappoint, and casdatifan could face similar difficulties 2.
    • If Gilead and other partners reduce their involvement, the company could face higher costs and fewer funding sources 2.

    What to watch

    • Results of the PEAK-1 study of casdatifan in renal cell carcinoma2027
    • Results of the PRISM-1 study of quemliclustat in pancreatic cancerfirst half of 2027
    • Entry of the first inflammation development candidate into the clinic2026
    • Evolution of liquidity and the terms of the loan agreementnext 10-K

    Products, market & competition

    AI-generatedAI-generated analysis (Claude) from cited public sources; it may contain errors. Not investment advice. As of 27 Oct 2026 · Model: claude-haiku-5-5.

    Possibly outdated: the newest document it read is from 05 Aug 2026; since then the company filed 8-K (04 Nov 2026 · results), 10-Q (04 Nov 2026), 8-K (21 Oct 2026 · results).

    The business

    Arcus Biosciences describes itself as a late clinical-stage biopharmaceutical company focused on differentiated molecules for patients with cancer and inflammatory and autoimmune diseases 1. It has not generated revenue from product sales, its revenue coming from upfront and milestone payments, R&D support and reimbursements from strategic partners 1. Its stated goal is to use internal small-molecule discovery to develop therapies with a meaningful impact on patients 1.

    Segments

    Inflammation and immunology

    The inflammation programs include five research and preclinical efforts directed at MRGPRX2, TNF, CCR6, CD89 and CD40 ligand, with the company expecting to advance a first development candidate into the clinic in 2026 1. The stated aim is to replace injectable biologics with oral small molecules, particularly in chronic spontaneous urticaria and atopic dermatitis 1.

    Partnerships and licences

    Gilead and Taiho hold rights to several programs, and Gilead's option rights ended in July 2026 for programs it did not continue to fund 2. The 2026 collaborations with Bristol Myers Squibb, Summit Therapeutics and AVEO extend the testing network for casdatifan 2.

    Market context

    The company operates in the oral renal cell carcinoma market, where approval of belzutifan has validated the HIF-2α target 1. Casdatifan is designed for greater efficacy, and the company estimates potential global peak sales above 2 billion USD 1 for the PEAK-1 setting and above 3 billion USD 1 for the TKI-free first-line setting.

    In inflammation, the company targets areas it describes as multi-billion dollar opportunities, such as chronic spontaneous urticaria and atopic dermatitis, where MRGPRX2 and TNF inhibition could displace injectable treatments 1. The timing and outcome of these programs depend on clinical success, which remains uncertain.

    Trends

    • Shift to oral therapies in immunologytailwind

      Developing oral small molecules to replace injectable biologics in inflammatory diseases could open large markets if clinical studies confirm efficacy.

    • Setbacks in anti-TIGIT combinationsheadwind

      The discontinuation of several Phase 3 studies with domvanalimab suggests the anti-TIGIT combination strategy may not succeed, which could reduce the value of some programs.

    • Collaborations with other antibody developersmixed

      Recent agreements with Bristol Myers Squibb, Summit Therapeutics and AVEO widen testing of casdatifan in combinations but may dilute control over the program.

    • Pressure on funding and debtheadwind

      Large net losses and a loan agreement with restrictive terms could make access to capital harder if studies are delayed.

    Competitive position

    In the HIF-2α space, Merck's belzutifan is the only approved inhibitor and the main reference point for casdatifan 1. In oncology, companies developing PD-1, PD-L1 or VEGF antibodies compete for the same treatment settings, while in inflammation the competition comes from established injectable biologics 12.

    The company notes that few other small-molecule TNF inhibitors are in development, which could give an advantage if its program reaches the clinic 1. Any advantage, however, depends on future study results.

    • Merck & Co., Inc.MRK

      Maker of belzutifan, the only approved HIF-2α inhibitor and the main reference point for casdatifan.

    • Gilead Sciences, Inc.GILD

      Strategic partner with rights to several programs and a significant shareholder in the company.

    • AstraZeneca plc

      Partner in studies with volrustomig and durvalumab, which compete with the dual PD-1 and CTLA-4 therapies the company is testing.

    • Summit Therapeutics

      Developer of ivonescimab, a PD-1/VEGF antibody tested with casdatifan and also a potential competitor in oncology.

    News & filings

    In the press

    The latest news item in our archive is from 24 Aug 2026; the newest SEC filing is from 04 Nov 2026. The press archive comes from the RSS feeds we follow and does not necessarily cover the latest event — the filings alongside do.

    SEC filings

    Sources

    1. [1] Form 10-K, fiscal year ended 2025-12-31 · SEC / Arcus Biosciences, Inc. · 25 Feb 2026
    2. [2] Form 10-Q, quarter ended 2026-06-30 · SEC / Arcus Biosciences, Inc. · 05 Aug 2026

    Figures computed by olivLaw from SEC filings and closing prices; the qualitative analysis is AI-generated from cited sources. Not investment advice.