Exelixis [EXEL]
2026-07-29 · every figure below traces to a named primary filing. No estimate is presented as a fact.
Q4 figures are derived (fiscal year minus the nine-month cumulative) because Exelixis, like most filers, does not tag a standalone Q4. All $000.
| Quarter ended | Total revenue | Operating income | Net income | Op margin |
|---|---|---|---|---|
| 2022-12-30 (Q4'22) | 423,917 | — | — | — |
| 2023-03-31 | 408,788 | — | — | — |
| 2023-06-30 | 469,848 | — | — | — |
| 2023-09-29 | 471,920 | — | — | — |
| 2023-12-29 (Q4'23) | 479,652 | — | — | — |
| 2024-03-29 | 425,226 | — | — | — |
| 2024-06-28 | 637,178 | — | — | — |
| 2024-09-27 | 539,542 | 136,075 | 117,973 | 25.2% |
| 2025-01-03 (Q4'24) | 566,755 | 163,206 | 139,861 | 28.8% |
| 2025-04-04 | 555,447 | 186,859 | 159,616 | 33.6% |
| 2025-07-04 | 568,261 | 213,576 | 184,848 | 37.6% |
| 2025-10-03 | 597,755 | 236,540 | 193,578 | 39.6% |
| 2026-01-02 (Q4'25) | 598,663 | 235,216 | 244,528 | 39.3% |
| 2026-04-03 | 610,812 | 251,341 | 210,467 | 41.1% |
Trailing-twelve-month series:
| TTM to | Revenue | Operating income | Net income | Op margin |
|---|---|---|---|---|
| 2023-12-29 | 1,830,208 | 170,885 | 207,765 | 9.3% |
| 2024-06-28 | 2,013,976 | 369,541 | 349,992 | 18.3% |
| 2025-01-03 | 2,168,701 | 604,617 | 521,267 | 27.9% |
| 2025-07-04 | 2,230,005 | 699,716 | 602,298 | 31.4% |
| 2026-01-02 | 2,320,126 | 872,191 | 782,570 | 37.6% |
| 2026-04-03 | 2,375,491 | 936,673 | 833,421 | 39.4% |
Read this table with §5 of the Research doc. The +30pp of margin in nine quarters is a completed cost reset (two restructurings, 2024 and August 2025, plus an abnormal FY2023 R&D load), not a repeatable curve. FY2026 guidance implies 38.1% — below the current run-rate.
From the Note 3 / Note 2 disaggregation of the FY2023 and FY2025 10-Ks, and MD&A milestone disclosure. $m.
| FY | CABOMETYX | COMETRIQ | Net product | License rev | Collab services | Total | Milestone rev | Ex-milestone total |
|---|---|---|---|---|---|---|---|---|
| 2021 | 1,054.1 | 23.2 | 1,077.3 | 250.0 | 107.8 | 1,435.0 | n/d | — |
| 2022 | 1,375.9 | 25.3 | 1,401.2 | 162.1 | 47.8 | 1,611.1 | 28.9 | 1,582.2 |
| 2023 | 1,614.9 | 13.9 | 1,628.9 | 178.6 | 22.7 | 1,830.2 | 15.0 | 1,815.2 |
| 2024 | 1,798.2 | 11.2 | 1,809.4 | 349.2 | 10.1 | 2,168.7 | 169.3 | 1,999.4 |
| 2025 | 2,113.4 | 9.4 | 2,122.8 | 214.4 | (17.1) | 2,320.1 | 14.3 | 2,305.8 |
| Q1'26 | 552.8 | 2.2 | 555.0 | 56.9 | (1.1) | 610.8 | n/d | — |
Collaboration services turns negative in FY2025 and Q1 FY2026 because the 3% Royalty Pharma royalty on Ipsen's and Takeda's sales is netted against it ($22.8m FY2025, $21.3m FY2024) and development-cost reimbursements collapsed ($3.7m FY2025 vs $25.8m FY2024). This is disclosure working correctly, not an anomaly.
Growth, headline versus clean:
| Window | Headline | Ex-milestone | Net product | CABOMETYX |
|---|---|---|---|---|
| FY2022 → FY2025 (3y CAGR) | 12.93% (= the screen's figure) | 13.4% | 14.85% | 15.4% |
| FY2023 → FY2025 (2y CAGR) | 12.6% | 12.7% | 14.2% | 14.4% |
| FY2024 → FY2025 | +7.0% | +15.3% | +17.3% | +17.5% |
The FY2024 distortion is one line item: a $150.0m commercial milestone from Ipsen on reaching $600.0m of cumulative cabozantinib net sales over four consecutive quarters in its territory, plus $2.2m (Canada) and $11.4m (EMA regulatory). Visible independently in the geography table — Europe was $318.6m in FY2024 versus $145.0m and $154.2m either side — and in Ipsen's share of total revenue: 15% FY2024, 8% FY2023, 7% FY2025.
| Party | Territory | Exelixis' economics | Cumulative to 2025-12-31 |
|---|---|---|---|
| Exelixis | U.S. | 100% of net product revenue | $2,122.8m in FY2025 alone |
| Ipsen (Feb 2016, amended) | ex-U.S., ex-Japan (incl. Canada from Dec 2016) | 22%–26% tiered royalty, resetting annually, separate Canada tiers; 35% development-cost share on opted-in trials | $210.0m upfront + $659.2m milestones + $837.9m royalties; $2.0m regulatory + up to $200.0m / CAD$23.5m sales milestones still available |
| Takeda (Jan 2017, amended) | Japan | 15%–24% on the first $300.0m of annual net sales, then 20%–30%, resetting annually; 20% of opted-in trial costs | $50.0m upfront + $138.0m milestones + $60.3m royalties; $108.0m first-commercial-sale milestones available |
| Royalty Pharma / GSK | worldwide | Exelixis PAYS a flat 3% royalty on worldwide net sales of any cabozantinib-containing product. From the October 2002 GSK collaboration; Royalty Pharma acquired the stream effective 2021-01-01 — non-U.S. for the full term, U.S. only through September 2026, then U.S. reverts to GSK at the same rate | Paid: $86.5m (FY2025), $75.5m (FY2024), $68.0m (FY2023) |
Where the royalty sits in the P&L — the reason it is easy to miss: - Exelixis' own U.S. sales → inside cost of goods sold. FY2025 COGS $83.697m on $2,122.8m of product revenue (96% gross margin), of which ~$63.7m is the 3% royalty and ~$20m is genuine product cost. - Ipsen's and Takeda's sales → netted against collaboration services revenue ($22.8m FY2025).
There is no profit share on cabozantinib anywhere. The KNSA structure (a profit-share arrangement capping the terminal margin by construction) is absent here. The only sharing is a 3-point gross royalty already embedded in the reported 37.6% / 39.4% operating margin.
| Assets | Liabilities & equity | ||
|---|---|---|---|
| Cash and cash equivalents | 226,152 | Accounts payable | 24,154 |
| Marketable securities | 551,055 | Accrued compensation | 87,512 |
| Trade receivables, net | 328,947 | Accrued clinical trial | 64,804 |
| Inventory | 26,605 | Rebates and fees due to customers | 65,892 |
| Prepaid and other current | 75,878 | Accrued collaboration | 28,327 |
| Total current assets | 1,208,637 | Other current | 100,286 |
| Non-current marketable securities | 649,144 | Total current liabilities | 370,975 |
| PP&E, net | 95,524 | Non-current operating lease | 169,541 |
| Deferred tax assets, net | 293,730 | Other non-current | 117,329 |
| Goodwill | 63,684 | Total liabilities | 657,845 |
| ROU assets and other | 282,874 | Common stock + APIC | 2,151,957 |
| AOCI | (415) | ||
| Accumulated deficit | (215,794) | ||
| Total assets | 2,593,593 | Total liab. & equity | 2,593,593 |
Net cash = 226,152 + 551,055 + 649,144 = $1,426,351k. There is no debt of any kind on this balance sheet. The screen's $1,029,692k is understated by $396,659k (27.8%) and could not be reconstructed from any combination of filed lines at any period end from Q1 FY2025 forward.
Accumulated deficit went from $(76,830)k to $(215,794)k in one quarter despite $210.5m of net income — because $430.4m of buybacks were charged against it. That is the buyback showing up on the balance sheet, not a loss.
| Date | Shares outstanding | Diluted WA (quarter) |
|---|---|---|
| 2023-06-30 | 320,253,000 | 319,247,000 (Q3'23) |
| 2025-01-03 | 281,732,000 | — |
| 2025-04-04 | 275,033,000 | 288,177,000 |
| 2025-07-04 | 270,132,000 | 284,393,000 |
| 2025-10-03 | 268,098,000 | 278,535,000 |
| 2026-01-02 | 262,483,000 | — |
| 2026-04-03 | 253,701,000 | 267,322,000 |
| 2026-04-27 (10-Q cover) | 251,355,083 | — |
−9.95% outstanding in five quarters. $2.16bn repurchased since March 2023, 76.7m shares retired at an average $28.14. October 2025 program of $750m completing May 2026; a further $750m authorised May 2026 to end-2027. At $56.51 that is ~13.3m more shares, another ~5%.
Consequence for the model: EPS grows faster than net income, and will keep doing so. Any forward EPS built off a static share count is wrong.
EPS cross-check (the brief's required scale test):
| Period | Net income | Diluted WA | Computed | Filed | Tie |
|---|---|---|---|---|---|
| Q1 FY2026 | $210,467k | 267,322k | $0.7873 | $0.79 | ✅ |
| FY2025 | $782,570k | 281,863k | $2.7764 | $2.78 | ✅ |
Issued 2026-01-11, reaffirmed unchanged 2026-05-05.
| FY2025 actual | FY2026 guidance | |
|---|---|---|
| Total revenues | $2.320bn | $2.525bn – $2.625bn |
| Net product revenues | $2.123bn | $2.325bn – $2.425bn (includes a 3.0% U.S. WAC increase effective 2026-01-01) |
| COGS, % of net product revenue | ~3.7% | 3.5% – 4.5% |
| R&D | ~$825m (incl. $40.8m SBC) | $875m – $925m (incl. $50.0m SBC) |
| SG&A | ~$520m (incl. $72.2m SBC) | $575m – $625m (incl. $75.0m SBC) |
| Effective tax rate | n/p | 21% – 23% |
| Ending cash and marketable securities | ~$1.65bn | not provided |
Guidance excludes all zanzalintinib revenue, stated explicitly in both releases.
Guidance-derived FY2026 operating income at the midpoints: $2,575m − $95m − $900m − $600m = $980m, a
38.1% margin — below the 39.4% TTM run-rate. Both opex lines are guided up in absolute dollars. The
screen's op_margin_delta_pp: +9.7 records a completed event; the company is not guiding a repeat.
The bridge that must hold: product revenue guidance of $2,325–2,425m against FY2025's $2,122.8m is +9.5% to +14.2%, midpoint +11.9%. Q1 delivered +8.1%. Q2–Q4 must therefore do +10.0% (low end) to +13.1% (midpoint) against $1,609.5m a year earlier. Tested 5 August 2026.
Daily trailing multiples: closing price × verified shares outstanding, less as-known net cash, over as-known TTM earnings stepped in at each 10-K/10-Q filing date (no look-ahead). Basic shares used throughout so the series is internally consistent.
| Window | Measure | Current | Min | p10 | p25 | Median | p75 | p90 | Max | Percentile |
|---|---|---|---|---|---|---|---|---|---|---|
| 2021-01-04 → 2026-07-28 (n=1,397) | Trailing P/E | 17.2x | 13.7 | 16.7 | 18.6 | 28.8 | 40.9 | 70.8 | 122.1 | 15th |
| 2021-01-04 → 2026-07-28 | EV/EBIT | 13.8x | 7.8 | 10.7 | 12.9 | 17.4 | 29.8 | 55.9 | 136.2 | 35th |
| 2024-01-02 → 2026-07-28 (n≈640) | Trailing P/E | 17.2x | 13.7 | — | — | 19.6 | — | — | 78.7 | 30th |
| 2024-01-02 → 2026-07-28 | EV/EBIT | 13.8x | 10.4 | — | — | 14.2 | — | — | 130.0 | 46th |
The full window is discarded and the post-2024 window is used. Exelixis' operating margin was 9.3% in
FY2023 and is 39.4% today; multiples computed on a near-zero denominator describe a different company. This
is a declared regime change, per references/regime-change-test.md — the median of 28.8x is an artifact
of the pre-inflection era and applying it would manufacture a target.
Corpus: EDGAR 8-K Exhibit 99.1 quarterly results press releases, 2023-02-07 → 2026-05-05, n = 17,
single source, never mixed. Alpha Vantage EARNINGS_CALL_TRANSCRIPT was unavailable (shared free-tier
25/day quota exhausted; the API returned its rate-limit Information payload). Per
references/mention-frequency.md the EDGAR first-party corpus is the documented fallback: complete,
near-constant length (3,265–5,053 words, mean 3,963), and prepared company language only — no Q&A, which
removes the analyst-question artifact entirely.
All values are per 10,000 words. Raw counts are never read; that is the ISRG failure mode.
| Term (per 10k words) | 23-02-07 | 23-05-09 | 23-08-01 | 23-11-01 | 24-01-08 | 24-02-06 | 24-04-30 | 24-08-06 | 24-10-29 | 25-01-13 | 25-02-11 | 25-05-13 | 25-07-28 | 25-11-04 | 26-01-12 | 26-02-10 | 26-05-05 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| transcript words | 5,053 | 3,514 | 3,265 | 3,604 | 3,343 | 4,842 | 3,837 | 4,111 | 4,240 | 3,688 | 4,622 | 3,743 | 4,239 | 4,227 | 3,545 | 4,396 | 4,065 |
| zanzalintinib | 37.6 | 14.2 | 15.3 | 8.3 | 26.9 | 22.7 | 23.5 | 19.5 | 37.7 | 70.5 | 54.1 | 37.4 | 37.7 | 37.9 | 81.8 | 61.4 | 98.4 |
| STELLAR | 13.9 | 5.7 | 6.1 | 5.5 | 6.0 | 14.5 | 5.2 | 14.6 | 18.9 | 29.8 | 34.6 | 29.4 | 44.8 | 14.2 | 56.4 | 43.2 | 86.1 |
| CRC | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 4.7 | 8.1 | 8.7 | 8.0 | 4.7 | 11.8 | 28.2 | 13.6 | 17.2 |
| colorectal | 0.0 | 0.0 | 3.1 | 0.0 | 6.0 | 2.1 | 2.6 | 2.4 | 2.4 | 2.7 | 4.3 | 8.0 | 7.1 | 4.7 | 5.6 | 4.5 | 4.9 |
| meningioma | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 4.7 | 5.6 | 2.3 | 9.8 |
| atezolizumab | 4.0 | 8.5 | 9.2 | 11.1 | 3.0 | 12.4 | 10.4 | 9.7 | 14.2 | 5.4 | 13.0 | 10.7 | 7.1 | 18.9 | 16.9 | 18.2 | 19.7 |
| Merck | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 28.3 | 5.4 | 21.6 | 5.3 | 0.0 | 0.0 | 11.3 | 18.2 | 19.7 |
| belzutifan | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 2.4 | 0.0 | 4.3 | 2.7 | 0.0 | 0.0 | 8.5 | 6.8 | 2.5 |
| neuroendocrine | 0.0 | 0.0 | 0.0 | 5.5 | 3.0 | 4.1 | 2.6 | 4.9 | 4.7 | 8.1 | 15.1 | 13.4 | 4.7 | 4.7 | 14.1 | 6.8 | 4.9 |
| cabozantinib | 65.3 | 74.0 | 55.1 | 58.3 | 53.8 | 70.2 | 67.8 | 68.1 | 80.2 | 65.1 | 62.7 | 45.4 | 28.3 | 28.4 | 36.7 | 43.2 | 44.3 |
| CABOMETYX | 13.9 | 17.1 | 36.8 | 30.5 | 26.9 | 18.6 | 23.5 | 26.8 | 18.9 | 19.0 | 23.8 | 45.4 | 35.4 | 42.6 | 25.4 | 27.3 | 14.8 |
| patent | 13.9 | 19.9 | 15.3 | 13.9 | 6.0 | 0.0 | 13.0 | 12.2 | 11.8 | 2.7 | 13.0 | 0.0 | 14.2 | 0.0 | 0.0 | 0.0 | 0.0 |
| MSN | 27.7 | 39.8 | 0.0 | 0.0 | 9.0 | 6.2 | 7.8 | 0.0 | 21.2 | 0.0 | 21.6 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| generic | 2.0 | 2.8 | 9.2 | 8.3 | 3.0 | 2.1 | 5.2 | 7.3 | 4.7 | 2.7 | 4.3 | 2.7 | 7.1 | 2.4 | 2.8 | 2.3 | 2.5 |
| royalt | 5.9 | 8.5 | 9.2 | 11.1 | 0.0 | 8.3 | 7.8 | 7.3 | 7.1 | 0.0 | 8.7 | 8.0 | 4.7 | 7.1 | 0.0 | 9.1 | 4.9 |
| Ipsen | 4.0 | 2.8 | 3.1 | 5.5 | 0.0 | 2.1 | 2.6 | 29.2 | 18.9 | 2.7 | 2.2 | 5.3 | 7.1 | 11.8 | 0.0 | 9.1 | 7.4 |
| Takeda | 4.0 | 2.8 | 3.1 | 2.8 | 0.0 | 2.1 | 2.6 | 2.4 | 2.4 | 0.0 | 2.2 | 2.7 | 0.0 | 0.0 | 0.0 | 2.3 | 2.5 |
| milestone | 11.9 | 17.1 | 6.1 | 5.5 | 38.9 | 12.4 | 13.0 | 26.8 | 9.4 | 35.2 | 17.3 | 8.0 | 9.4 | 4.7 | 36.7 | 18.2 | 12.3 |
| repurchase | 0.0 | 22.8 | 24.5 | 22.2 | 38.9 | 18.6 | 31.3 | 38.9 | 14.2 | 16.3 | 17.3 | 26.7 | 23.6 | 37.9 | 22.6 | 20.5 | 27.1 |
| XB628 | 5.9 | 5.7 | 0.0 | 0.0 | 6.0 | 2.1 | 2.6 | 0.0 | 0.0 | 5.4 | 2.2 | 8.0 | 16.5 | 2.4 | 11.3 | 0.0 | 0.0 |
| XL309 | 0.0 | 0.0 | 0.0 | 13.9 | 23.9 | 6.2 | 7.8 | 7.3 | 2.4 | 24.4 | 6.5 | 8.0 | 11.8 | 2.4 | 8.5 | 0.0 | 0.0 |
| ADC | 11.9 | 0.0 | 0.0 | 0.0 | 15.0 | 6.2 | 10.4 | 12.2 | 4.7 | 10.8 | 0.0 | 0.0 | 4.7 | 2.4 | 11.3 | 0.0 | 0.0 |
| prostate | 4.0 | 2.8 | 3.1 | 5.5 | 6.0 | 8.3 | 10.4 | 2.4 | 7.1 | 5.4 | 0.0 | 0.0 | 0.0 | 0.0 | 2.8 | 0.0 | 4.9 |
| guidance | 5.9 | 8.5 | 9.2 | 8.3 | 44.9 | 10.3 | 13.0 | 12.2 | 21.2 | 43.4 | 13.0 | 24.0 | 9.4 | 14.2 | 45.1 | 11.4 | 12.3 |
EMERGING — zanzalintinib (trough 8.3 → 98.4, 11.9x), STELLAR (5.2 → 86.1, 16.6x), CRC (zero
through 24-08, first material 24-10, now 17.2), meningioma (zero through 25-07, first appears 25-11, now
9.8), atezolizumab (4.0 → 19.7), Merck/belzutifan (zero before 24-10).
DECAYING — cabozantinib (80.2 peak 24-10 → 44.3, −45%), CABOMETYX (45.4 peak 25-05 → 14.8, the
lowest reading since the first release in the series), patent (zero in each of the last four releases),
MSN (zero in each of the last six).
STABLE — repurchase (high and constant, 14–39, the one thing management never stops saying),
generic (2–9 throughout, no trend), royalt, Takeda.
SPIKE, EXPLAINED — Ipsen at 29.2 in the 24-08-06 release. That is the quarter of the $150.0m Ipsen
commercial milestone. The mention series and the milestone-revenue table (§2) corroborate each other,
which is the standard the method requires.
ARTIFACT, DISCARDED — NET was in the initial term set at 24–118 per 10k words and was removed: it
collides with "net product revenues" and "net income" and its counts are almost entirely the homonym. This is
exactly the word-boundary failure the reference warns about. neuroendocrine is the clean proxy and it is
too noisy (0.0 → 15.1 → 4.9) to call a trend.
patent been absent from four consecutive results releases, and MSN from six — the exact
window in which the appeal deciding the company's terminal value was briefed, consolidated, settled with
one defendant, and argued? Investigated: the litigation is disclosed in full in 10-K Note 12 and 10-Q
Note 11, and the CAFC docket (No. 2025-1236) confirms argument on 2026-06-04. So it is not
concealment, and this memo does not claim it is. The narrower read: management's prepared language has
moved entirely to the second franchise while the first franchise's terminal date remains unresolved.CABOMETYX at a series low in the same release where zanzalintinib hits a series high? The
2026-05-05 release mentions the marketed product that generates 90.5% of revenue 14.8 times per 10k words
and the unapproved one 98.4 times — a 6.6x ratio. In 2023-05 the ratio was 0.83x.meningioma from nothing to 9.8 — corroborated: STELLAR-201 was initiated, per the 2026-05-05
release, in an indication with no approved systemic therapy.repurchase never decays. Corroborated by the balance sheet: $430.4m in Q1 FY2026 alone, $2.16bn
since March 2023, $1.5bn more authorised.| Field | Screen | Verified | Δ |
|---|---|---|---|
revenue_ttm |
2,375,491,000 | 2,375,491,000 | 0 |
shares |
251,355,083 | 251,355,083 | 0 |
spot |
56.525 | 56.51 | −0.03% |
revenue_cagr_demonstrated |
12.9 | 12.93 | ✅ |
vol_252d_pct |
38.6 | 39.3 | +0.7 |
op_margin_pct |
37.6 (FY2025) | 39.4 (TTM) | basis mismatch |
net_cash |
1,029,692,000 | 1,426,351,000 | −$396,659,000 (−27.8%) |
ev |
13,178,154,067 | 12,776,749,000 | +$401.4m (+3.1%) |
ev_sales |
5.55 | 5.38 | overstated |
ev_ebit |
14.8 | 13.6 | overstated |
terminal_margin |
0.376 (scan_all_v2) / 0.229 (scan_final, capped) |
— | two runs, opposite verdicts |
required_cagr_pct |
2.9 (scan_all_v2) / 13.6 (scan_final) |
2.3 at 20.6x / 13.9 at 12.0x | driven by the exit multiple, not the margin |
valuation |
PASS (scan_all_v2) / FAIL (scan_final) |
INDETERMINATE | exit multiple UNIDENTIFIED |
data_quality_ok |
false (scan_final) |
— | the screen flagged itself and the flag was correct |
Three findings for the scanner, in order of value:
op_margin_pct is computed on the fiscal year while revenue_ttm is computed on the trailing twelve
months. Mixing bases understates the margin by 1.8pp here and will do so systematically on any name
whose margin is moving.