Arcus Biosciences, Inc. (RCUS) Stock Price & How to Invest
Last updated July 2026
Short answer
Arcus Biosciences is a Hayward, California clinical-stage oncology company whose equity value now rests almost entirely on one wholly owned molecule: casdatifan, an oral HIF-2alpha inhibitor in Phase 3 for clear cell kidney cancer. A screener sees ~$117 million of trailing revenue against a ~$3.9 billion market capitalization and prints a 33x sales multiple. That trailing figure is the amortization of upfront and milestone cash already banked from Gilead and Taiho, and the deferred revenue balance feeding it has fallen from $319 million at December 31, 2024 to $56 million at June 30, 2026, with full-year 2026 revenue guided to $65 million to $75 million. Arcus has never recorded a dollar of product sales.
RCUS stock price
As of 2026-08-21, Arcus Biosciences, Inc. (RCUS) last closed at $30.34, up 188.1% over the past year. Over the past 52 weeks it has traded between $10.15 and $31.08.
Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or Arcus Biosciences, Inc.'s investor relations page. Walnut is informational, not investment advice.
What does Arcus Biosciences, Inc. (RCUS) do?
Arcus runs a single reportable segment out of Hayward, California with roughly 600 employees, and it has never generated revenue from product sales. Every dollar recognized since the 2018 IPO has come from research, collaboration and license arrangements, principally with Gilead Sciences and Japan's Taiho Pharmaceutical. Gilead paid $725 million in 2022 to license the anti-TIGIT program (domvanalimab and AB308), the adenosine receptor program (etrumadenant) and the CD73 program (quemliclustat), plus a further $100 million option continuation payment received in 2024. Taiho holds rights across Japan and much of Asia excluding China to five Arcus programs, exercised its casdatifan option in the fourth quarter of 2025 for $15 million, and became obligated in the second quarter of 2026 to pay a $30 million clinical milestone tied to the Phase 3 PEAK-1 study. Those payments sit in deferred revenue and are released to the income statement as Arcus performs the underlying research, so reported revenue tracks the pace of laboratory and trial work rather than any commercial activity. The portfolio itself has narrowed sharply. Gilead returned the etrumadenant license in 2025, three Phase 3 studies of domvanalimab have been stopped since December 2025, and casdatifan, which Arcus owns outright, is what remains.
What the market is paying for sits in one indication. Casdatifan is an oral HIF-2alpha inhibitor for clear cell renal cell carcinoma, a class in which Merck's belzutifan is the only approved drug, and Arcus leads global development while working through regional partners. PEAK-1, a Phase 3 comparing casdatifan plus cabozantinib against cabozantinib alone in patients who have already had immunotherapy, is expected to complete enrollment by the end of 2026, and a second registrational study, PEAK-20, in first-line disease with nivolumab and ipilimumab, is meant to start in the same window. Management has publicly framed the commercial opportunity at $5 billion to $10 billion. The reported numbers move the other way: revenue fell 74% year over year in the second quarter to $41 million, the trailing twelve-month net loss is ~$460 million, and cash plus marketable securities dropped from $1.01 billion at the end of 2025 to $775 million at June 30, 2026. The company guides to roughly $600 million at year-end 2026 and to a runway lasting into at least the second half of 2028, which places its next financing decision after the data that will define the asset.
What's driving Arcus Biosciences, Inc. (RCUS)?
1. Casdatifan carries the whole valuation
Arcus owns casdatifan outright outside the Taiho Territory and leads its global development. The near-term calendar is dense. An ARC-20 data package expected in October 2026 covers initial first-line efficacy for casdatifan plus zimberelimab, mature objective response rate and first progression-free survival data from the second-line casdatifan plus cabozantinib cohort (roughly 45 patients with at least 18 months of follow-up), and overall survival updates from the late-line monotherapy cohorts. PEAK-1 should finish enrolling by year end and PEAK-20 is scheduled to begin in the same window. A Nature publication tied deep and sustained suppression of serum erythropoietin to higher response rates and longer progression-free survival, the mechanistic case Arcus makes for potency against belzutifan. Management sizes the opportunity at $5 billion to $10 billion.
2. Gilead has stepped back without selling
Gilead's option rights over the broader Arcus pipeline ended on July 14, 2026 after Gilead declined to make the option continuation payment, so the CCR6, CD89 and CD40L programs are no longer promised to anyone. On August 5, 2026 the two companies signed a new investor rights agreement under which Gilead gave up its right to designate directors. Dietmar Berger, Johanna Mercier and Linda Higgins all resigned from the board that day, and the board shrank from eleven seats to eight. Gilead still held approximately 24.7% of the shares (31,424,760) at June 30, 2026 and keeps existing licenses to domvanalimab, AB308, quemliclustat and zimberelimab, plus time-limited options on AB801, AB598 and a TNF inhibitor. The stake stays; the influence does not.
3. The TIGIT program is finished, and spending is coming down with it
Three Phase 3 studies of domvanalimab have been stopped in nine months: STAR-221 in December 2025 after an interim analysis showed no benefit over standard of care, STAR-121 in April 2026 for futility, and the AstraZeneca-partnered PACIFIC-8 in August 2026. R&D expense fell to $113 million in the second quarter of 2026 from $139 million a year earlier, and to $235 million for the half from $261 million. The segment disclosure shows where the money went out: early-stage and preclinical spend halved to $39 million for the half from $80 million, while late-stage program spend eased to $111 million from $129 million. Management expects R&D to keep declining near term as the domvanalimab studies wind down, offset partly by heavier casdatifan and immunology investment.
4. The balance sheet is funded past the decisive data
Cash and marketable securities stood at $775 million on June 30, 2026 against $198 million of current liabilities and $101 million of long-term debt. Operating cash use was $257 million in the first half, roughly flat against $265 million a year earlier. The Hercules facility runs to $250 million in four tranches, of which $100 million is drawn; it matures in September 2030 and is interest-only until at least September 2028, and two of the remaining $50 million tranches become available only on clinical or regulatory milestones. An equity distribution agreement permits up to $200 million of at-the-market sales. Arcus already used the equity market hard in 2025, issuing 29.4 million shares across two underwritten offerings for approximately $438 million gross. The share count has gone from 92.2 million at the end of 2024 to 127.3 million on July 30, 2026.
What are the risks to Arcus Biosciences, Inc. (RCUS)?
Concentration is the central risk. Three Phase 3 domvanalimab studies read out badly inside nine months, and Arcus itself warns in the filing that Phase 2 results were not predictive: EDGE-Gastric showed median overall survival beyond two years against Phase 3 benchmarks of 13 to 14 months, yet STAR-221 was still stopped in December 2025 for no benefit over standard of care. The same caution attaches to reading ARC-20 across into PEAK-1 and PEAK-20. Competitively, casdatifan enters a class Merck already occupies with belzutifan, which carries approval, a sales force and years of prescriber familiarity. On the financial side the revenue line is mechanically shrinking: deferred revenue fell to $56 million at June 30, 2026 from $78 million at year end and $319 million two years before, and partnership reimbursements that offset R&D dropped to $36 million for the half from $71 million, so reported expense can worsen even where gross spending falls. The Hercules loan is secured by substantially all of the company's assets and carries a minimum cash covenant beginning in July 2027, conditionally waived only if market capitalization exceeds a specified threshold, tying a financing covenant to the share price at the moment a data disappointment would bite hardest. Gilead's ~24.7% position is registered and no longer accompanied by board seats, removing one reason for it to sit still. The $200 million at-the-market program and the 29.4 million shares issued during 2025 show how this company funds itself. Accumulated deficit reached $1.704 billion at June 30, 2026, the IRS is examining the 2023 tax year, and standard-of-care comparators including cabozantinib, carboplatin and oxaliplatin are flagged in the filing as difficult to source for trials.
What is the Arcus Biosciences, Inc. (RCUS) forecast?
12 analysts publish price targets on RCUS, averaging $38.33 against a $30.34 price as of August 2026, or +26.3%. The published targets run from $23.00 to $47.00, a moderate spread, and the ratings split 10 buy, 3 hold, 0 sell. Over the last six months there have been 8 raises and 0 cuts among the published actions. A price target is what an analyst published on a date, not a prediction, and sell-side ratings skew positive across the whole market.
Read the full RCUS forecast and price target for the target table, the recent rating actions by firm, and how the consensus has shifted.
Is RCUS a buy or a sell?
We give no verdict on Arcus Biosciences, Inc.. Both cases are real, which is why the question is contested at all, so here is the strongest version of each.
The case for buying. Casdatifan carries the whole valuation. Arcus owns casdatifan outright outside the Taiho Territory and leads its global development. The most optimistic published target, $47.00, assumes this works close to its best case.
The case against. Concentration is the central risk. The most pessimistic target, $23.00, is roughly what RCUS is worth if this bites instead.
Read the full bull and bear case on RCUS, including what would have to change to break either one. Walnut is not an investment adviser.
How is Arcus Biosciences, Inc. (RCUS) valued? (approximate, August 2026)
A simple financial snapshot. These are approximations and refresh quarterly; for current figures see Arcus Biosciences, Inc.'s investor relations page or your broker.
- Revenue (TTM): ~$117 million for the twelve months to June 30, 2026, versus $247 million in fiscal 2025 and $258 million in fiscal 2024. All of it is collaboration revenue from Gilead and Taiho; Arcus has never recorded product sales. Second-quarter 2026 revenue was $41 million against $160 million a year earlier, a 74% decline, because the prior-year quarter included $152 million of license and development services revenue recognized in one go.
- 2026 guidance and the deferred revenue behind it: Management guides GAAP revenue of $65 million to $75 million for full-year 2026, which would be roughly a 70% decline from 2025. The deferred revenue balance that feeds the line stood at $56 million at June 30, 2026 ($19 million current and $37 million noncurrent), down from $78 million at December 31, 2025 and $319 million at December 31, 2024. Remaining performance obligations were disclosed at $256 million at the end of 2025.
- Operating expenses: R&D was $113 million in the second quarter of 2026 and $235 million for the half, down from $139 million and $261 million. G&A was $24 million and $53 million against $29 million and $57 million. Full-year 2025 R&D was $523 million and G&A $110 million. Partnership reimbursements offsetting R&D fell to $36 million for the half from $71 million, and late-stage program spend came in at $111 million versus $129 million.
- Earnings and EPS: Net loss of $91 million, or $0.72 per share, in the second quarter of 2026, and $219 million, or $1.74 per share, for the first half on 125.7 million weighted-average shares. The trailing twelve-month loss is ~$460 million, or ~$3.86 per share. Fiscal 2025 produced a $353 million loss and fiscal 2024 a $283 million loss. Accumulated deficit stands at $1.704 billion. No P/E ratio exists and no income tax was recorded, given forecast full-year net operating losses.
- Cash flow and balance sheet: Cash, cash equivalents and marketable securities of $775 million at June 30, 2026, made up of $150 million cash, $552 million current marketable securities and $73 million long term, down from $1.01 billion at December 31, 2025. Operating cash use was $257 million in the first half. Total assets were $924 million, current liabilities $198 million, long-term debt $101 million under the Hercules facility maturing September 2030, and stockholders' equity $464 million. Guidance is ~$600 million of cash at year-end 2026 and runway into at least the second half of 2028.
- Market pricing: The shares changed hands around $30 in late August 2026 against a 52-week range of roughly $9.92 to $31.74, giving a market capitalization near $3.9 billion on 127,333,376 shares outstanding as of July 30, 2026. Enterprise value is approximately $3.2 billion once ~$775 million of cash and ~$101 million of debt are netted. There is no P/E, no EV/EBITDA and no dividend, since the company loses money at the operating line. Gilead's ~24.7% holding means the tradeable float is materially smaller than the headline share count.
Every conventional multiple here is either undefined or misleading. The ~33x trailing sales figure a screener prints rests on a revenue stream management has already guided down to $65 million to $75 million for 2026, with no commercial engine behind it. The ~$3.2 billion enterprise value instead represents a probability-weighted view of casdatifan in clear cell kidney cancer, a market Arcus sizes at $5 billion to $10 billion, discounted for Phase 3 risk and for the cash the company expects to consume between now and the second half of 2028.
Who competes with Arcus Biosciences, Inc. (RCUS)?
Approved and developing therapies in clear cell kidney cancer
Casdatifan's direct comparator is belzutifan, marketed by Merck as WELIREG and the only FDA-approved HIF-2alpha inhibitor, which sets both the efficacy bar and the commercial template. Beyond that class, treatment of advanced clear cell RCC is built on combinations Arcus has to position around: Bristol Myers Squibb's nivolumab plus ipilimumab, Merck's pembrolizumab regimens, Exelixis's cabozantinib (which doubles as the comparator and the combination partner in PEAK-1), Pfizer's axitinib, and tivozanib from AVEO Oncology, an LG Chem company that agreed in July 2026 to supply the drug for an ARC-20 cohort in patients previously treated with belzutifan. Earlier-stage entrants are circling the same biology, including HiberCell's HC-7366, which is being studied in combination with belzutifan.
PD-1 and VEGF bispecifics, partners and threats at once
The most crowded area in solid-tumor immuno-oncology right now is the PD-1/VEGF bispecific class, and Arcus has chosen to run toward it. Summit Therapeutics agreed in July 2026 to pair ivonescimab with casdatifan in a new first-line ccRCC cohort of ARC-20. In June 2026 Arcus agreed to supply casdatifan into the Bristol Myers Squibb-sponsored ROSETTA RCC-208 study of pumitamig (BNT327/BMS-986545), the PD-L1/VEGF-A bispecific that BioNTech and Bristol Myers Squibb are developing together. Those arrangements give casdatifan optionality across regimens at low cost. They also mean the same molecules could eventually anchor frontline kidney-cancer regimens that carry no HIF-2alpha inhibitor at all.
Clinical-stage oncology companies competing for capital and partners
Arcus competes for investor money and for pharma partnership dollars with a cohort of loss-making oncology developers whose stories are similarly concentrated, among them Summit Therapeutics, Revolution Medicines and Nuvalent, each defined by a narrow lead franchise and each spending well ahead of revenue. Exelixis sits at the far end of the same path as the clearest example of what commercial success in kidney cancer looks like, with an approved product and genuine product revenue rather than deferred collaboration income. Gilead, Taiho and AstraZeneca appear on both sides of the ledger, funding Arcus programs while running competing assets of their own, which is a normal condition of oncology partnerships and a live conflict all the same.
What stocks are similar to Arcus Biosciences, Inc. (RCUS)?
Other names that sit close to RCUS: same theme, named as a direct competitor, or held beside it in the same funds. Each entry says which. Worth a look if you are thinking about diversification within a thesis rather than concentration on one ticker.
How to invest in Arcus Biosciences, Inc. (RCUS)
There are three common ways to get RCUS exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it, which spreads the position across many companies. Or build it into a focused thematic portfolio, so RCUS sits alongside other stocks that express the same thesis.
Walnut takes the portfolio route. Describe a thesis where RCUS fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.
New to this? Start with how to invest in stocks, see how to analyze a stock with AI, or compare the best AI stock analyzers.
The bottom line on Arcus Biosciences, Inc. (RCUS)
As of August 2026, RCUS trades as a single-asset kidney-cancer position backed by ~$775 million of cash rather than as a revenue multiple. The collaboration line on the income statement is running off by design, and the October casdatifan data package is what the ~$3.9 billion market value is being set against.
More on Arcus Biosciences, Inc. (RCUS)
Whether RCUS is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is RCUS a buy or a sell?, and where the stock could go from here in the RCUS stock forecast.
For income investors, whether RCUS pays a dividend and how the payout looks is covered in does RCUS pay a dividend? And to weigh RCUS against a peer, read the full side-by-side comparisons: RCUS vs BMY and RCUS vs EXEL.
Wondering how RCUS fits the portfolio you already own? Walnut is an AI investing app that connects your brokerage read-only and answers questions like that about your actual holdings: overlap, concentration, and how each position tracks the S&P 500. Compare the best AI portfolio analyzers or see the best AI investing apps in 2026.
Investing in Arcus Biosciences, Inc. with AI
Connect the broker you already use and ask Walnut's AI how RCUS fits what you actually hold: whether you own it already through a fund, what it would do to your concentration, and how it has tracked the S&P 500. Read-only by default, and you approve anything before it reaches your broker.
FAQ
What does Arcus Biosciences do?
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Arcus Biosciences is a clinical-stage biopharmaceutical company based in Hayward, California, listed on the New York Stock Exchange under RCUS, with roughly 600 employees and one reportable segment. It designs small molecules and antibodies for cancer and, more recently, for inflammatory and immunological disease. Nothing in the portfolio is approved or sold, so the entire revenue line comes from collaboration and license agreements with Gilead Sciences, Taiho Pharmaceutical and AstraZeneca. The lead asset is casdatifan, an oral HIF-2alpha inhibitor in Phase 3 for clear cell renal cell carcinoma, which Arcus owns outside Japan and much of Asia. Other programs include quemliclustat in pancreatic cancer, licensed to Gilead, and early immunology candidates aimed at MRGPRX2, TNFR1, CCR6, STAT6, CD89 and CD40L.
Why did RCUS stock go up so much?
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The re-rating tracked the pipeline rather than the income statement. Over the twelve months to August 2026 the shares ran from a 52-week low near $9.92 toward the top of the range around $31.74 while revenue fell 74% year over year. Two things drove it. Casdatifan produced encouraging Phase 1/2 evidence in clear cell kidney cancer, including a Nature paper linking sustained erythropoietin suppression to higher response rates and longer progression-free survival, and Arcus kept full rights to the molecule instead of seeing it optioned away to a partner. At the same time, the failure of three Phase 3 domvanalimab studies removed a distraction and a large share of the spending attached to it. The market marked one asset up while writing another off.
Is Arcus Biosciences profitable?
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No. Arcus has never generated revenue from product sales and reported a net loss of $91 million, or $0.72 per share, in the second quarter of 2026, plus $219 million for the first half. The trailing twelve-month loss is roughly $460 million. Fiscal 2025 produced a $353 million loss on $247 million of revenue, and fiscal 2024 a $283 million loss on $258 million. Accumulated deficit reached $1.704 billion by June 30, 2026. One quarter, the second of 2025, came in near break-even, but only because $152 million of previously deferred Gilead and Taiho payments happened to be recognized inside it. Sustained profitability would require an approved and selling product, which the company does not yet have.
What is casdatifan and when is the next data readout?
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Casdatifan is an oral small molecule that inhibits HIF-2alpha, a transcription factor that drives tumor growth in clear cell renal cell carcinoma. Arcus owns it outright outside the Taiho Territory of Japan and parts of Asia. The near-term catalyst is an ARC-20 data package expected in October 2026, covering initial first-line efficacy for casdatifan plus zimberelimab, mature objective response rate and first progression-free survival data from the second-line casdatifan plus cabozantinib cohort of roughly 45 patients with at least 18 months of follow-up, and overall survival updates from late-line monotherapy. The registrational Phase 3, PEAK-1, compares casdatifan plus cabozantinib against cabozantinib alone in immunotherapy-experienced patients and should finish enrolling by the end of 2026. A second Phase 3, PEAK-20, is due to start in the same window.
Does Gilead own Arcus Biosciences?
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Gilead Sciences held approximately 24.7% of Arcus common stock, or 31,424,760 shares, as of June 30, 2026, making it by far the largest holder, though it does not control the company. The relationship narrowed considerably during 2026. Gilead's option rights over the broader Arcus pipeline lapsed on July 14, 2026 after it declined to make the continuation payment, and on August 5, 2026 the two signed a new investor rights agreement removing Gilead's right to designate directors. All three Gilead-designated board members resigned that day and the board went from eleven seats to eight. Gilead keeps its existing licenses to domvanalimab, AB308, quemliclustat and zimberelimab, plus time-limited options on AB801, AB598 and a TNF inhibitor program.
Who are Arcus Biosciences' competitors?
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In its lead indication Arcus competes most directly with Merck, whose belzutifan (WELIREG) is the only approved HIF-2alpha inhibitor and therefore the benchmark casdatifan has to beat on efficacy, tolerability and dosing. The wider standard of care in advanced clear cell kidney cancer is set by Bristol Myers Squibb's nivolumab plus ipilimumab, Merck's pembrolizumab regimens, Exelixis's cabozantinib and Pfizer's axitinib. Newer PD-1/VEGF bispecifics from Summit Therapeutics and from the BioNTech and Bristol Myers Squibb partnership could reshape frontline treatment, although Arcus has struck cohort collaborations with both rather than competing head-on for now. For capital and partnership attention, the peer group is other concentrated clinical-stage oncology developers.
Does RCUS pay a dividend?
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No. Arcus Biosciences pays no dividend and has never declared one. The company loses money at every line, used $257 million of cash in operations during the first half of 2026 alone, and is funding one Phase 3 study plus a second registrational trial due to start by year end. A capital return of any kind would sit badly against that position, and the Hercules loan agreement, secured by substantially all of the company's assets and carrying a minimum cash covenant that begins in July 2027, adds a further constraint. Anyone holding RCUS is exposed entirely to share price movement driven by clinical results, partnership terms and financing decisions. Income allocations in a portfolio are typically met elsewhere, from established pharmaceutical companies or healthcare funds that distribute.
Will Arcus Biosciences need to raise more money?
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Probably, though not immediately. Arcus reported $775 million in cash and marketable securities at June 30, 2026, guides to roughly $600 million at year-end, and states a runway into at least the second half of 2028. Two funding channels sit alongside that. An equity distribution agreement permits up to $200 million of at-the-market share sales, and $150 million of the $250 million Hercules term facility remains undrawn, although two of those $50 million tranches become available only on clinical or regulatory milestones. Recent history points to equity as the preferred route: Arcus issued 29.4 million shares in two underwritten offerings during 2025 for approximately $438 million gross, and the share count rose from 92.2 million at the end of 2024 to 127.3 million by July 30, 2026. Strong casdatifan data would make the next raise cheaper.
Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with Arcus Biosciences, Inc.'s investor relations page or your broker before making investment decisions.