Phase Space AI

Financial Model Notes

Exelixis [EXEL]

Exelixis, Inc. [EXEL] — Financial Model Notes

2026-07-29 · every figure below traces to a named primary filing. No estimate is presented as a fact.


1. Quarterly revenue and profitability, built from XBRL

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.


2. Revenue mix and the milestone adjustment

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.


3. Cabozantinib economics — who gets what

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. salesinside 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.


4. Balance sheet — Q1 FY2026 (period ended 2026-04-03), $000

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.


5. Share count and buyback

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

6. FY2026 guidance — the forward model, from the company

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.


7. Own-multiple history — method and full result

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.


8. Transcript mention-frequency — full 17-quarter series

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 / decaying / stable, and open questions

EMERGINGzanzalintinib (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).

DECAYINGcabozantinib (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).

STABLErepurchase (high and constant, 14–39, the one thing management never stops saying), generic (2–9 throughout, no trend), royalt, Takeda.

SPIKE, EXPLAINEDIpsen 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, DISCARDEDNET 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.

Open questions this generated, before a thesis existed

  1. Why has 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.
  2. Why is 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.
  3. 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.
  4. repurchase never decays. Corroborated by the balance sheet: $430.4m in Q1 FY2026 alone, $2.16bn since March 2023, $1.5bn more authorised.

9. Reconciliation to the Tier-1 screen

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:

  1. Net cash is wrong again — the tenth consecutive name. Here the error is $396.7m on a name where marketable securities are split across current ($551.1m) and non-current ($649.1m) lines and there is no debt at all. The verified figure comes straight off one balance sheet.
  2. 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.
  3. The exit multiple is never sensitised, and it decides every verdict. Both screen runs varied the terminal margin (37.6% vs a 22.9% industry cap) and produced opposite verdicts, while leaving the exit multiple fixed at 20.6x — the parameter that moves the required CAGR from 30.9% to −0.8%. On this name the 20.6x anchor is not merely unsensitised, it is unidentified: a 542-name set matched on +12.9% trailing growth cannot bracket the exit-year growth of an asset whose patent estate expires eighteen months before the exit year.