Exelixis
Market cap $17.0B 244.0M shares (10-Q, Oct 19, 2026) × $69.57 close Nov 6, 2026
Most recent annual filing: 2026-02-15
- XL557 / XB773 IND filing2026XL557 / XB773 IND filing, 2026, notable
- STELLAR-304 topline1Q 2027STELLAR-304 topline, 1Q 2027, material
- Zanzalintinib FDA approvalMar 3, 2027Zanzalintinib FDA approval, Mar 3, 2027, material
Bar width shows how precise the guidance is — a pin is a stated date, a wide band a six-month window. Deeper blue means more of the thesis rides on the event; it is not a view on the stock.
Pipeline (23 active programs)
CABOMETYX
COMETRIQ · cabozantinibCOTELLIC
cobimetinibMINNEBRO
esaxerenonezanzalintinib
XL309
XB010
- Undisclosed indication
XB628
XB371
ADU-1805
- Undisclosed indication
XB773
- Undisclosed indication
XL558
- Undisclosed indication
XB404
- Undisclosed indication
Technology platforms
SAFEbody · Adagene
Adagene's SAFEbody technology platform for generating masked monoclonal antibodies for ADC or other innovative biotherapeutic development against Exelixis-nominated oncology targets
SMARTag · Catalent
Catalent's SMARTag site-specific bioconjugation technology platform for development of multiple ADCs for oncology
B-Body · Invenra
Invenra's B-Body technology platform for discovery and development of novel binders and multispecific antibodies for oncology
Discontinued (4)
- zanzalintinib — Squamous Cell Carcinoma of the Head and Neck · study will not proceed to phase 3 based on emerging data, competition, and assessment of other commercial opportunities
- XL495 — undisclosed · discontinued further development based on early clinical data
- XB064 — undisclosed · discontinued further development
- XB033 — undisclosed · discontinued further development
Capital (as filed)
- Cash
- $305M cash and cash equivalents · Oct 2, 2026 (10-Q)
- Short-term investments
- $587M Oct 2, 2026
- Long-term investments
- $508M Oct 2, 2026
- Operating cash flow
- $280M quarter Jul 3, 2026 → Oct 2, 2026, year-to-date difference (10-Q)
- As stated in coverage
- $1.40B cash per the update of Oct 29, 2026 — the company's own words as read there, not the filed figure
Cash, investments and operating cash flow are the company's own XBRL facts as filed with the SEC, each shown with its period end and tag. As-stated figures come from the company's own words as read in Biotech Distilled coverage, dated, and routinely count securities and planned financing that a balance sheet does not. Offering rows are the SEC cover pages as filed. Not investment advice. Figures as of Nov 7, 2026.
Biotech Distilled coverage (9)
- 2026-10-30 UPDATE: Exelixis (EXEL) - The Wolves Found a Side Door 🔒 Paid
- 2026-09-11 UPDATE: Exelixis (EXEL) - The Christmas Present Gets Pushed to Spring 🔒 Paid
- 2026-08-31 UPDATE: Exelixis (EXEL) - The Wolves Get Pushed Back to 2030 🔒 Paid
- 2026-08-06 UPDATE: Exelixis (EXEL) - The Mea Culpa on STELLAR-303 🔒 Paid
- 2026-06-22 UPDATE: Exelixis (EXEL) - STELLAR-303 Clears the Second Bar
- 2026-05-06 UPDATE: Exelixis (EXEL) - Q1 prints another cash-gusher quarter and the Board just stacked another $750M on the buyback pile. 🔒 Paid
- 2026-02-14 UPDATE: Exelixis (EXEL) - The Receipts Are In 🔒 Paid
- 2026-02-07 UPDATE: Exelixis (EXEL) - The Clock Starts Now 🔒 Paid
- 2026-01-30 Exelixis Inc.(EXEL): Scientific Deep Dive for Zanza and Pipeline Products 🔒 Paid
Articles open on Substack. Some are subscriber-only; those marked ★ Distilled Pro are for Distilled Pro members.
Verdict history (9 calls)
Every verdict Biotech Distilled has published on Exelixis, oldest first — the full history, never a selection. How calls are scored: the track record.
- 2026-01-30 Buy core Exelixis Inc.(EXEL): Scientific Deep Dive for Zanza and Pipeline Products Cash-printing machine with no dilution risk, a de-risked balance sheet, and a clear catalyst in the Zanza CRC launch that could bridge the 2030/2031 patent cliff.
- 2026-02-07 Buy core UPDATE: Exelixis (EXEL) - The Clock Starts Now FDA acceptance of the Zanza NDA with a concrete October 15, 2026 PDUFA date validates the buy thesis and de-risks the timeline.
- 2026-02-14 Buy core UPDATE: Exelixis (EXEL) - The Receipts Are In Strong Q4/FY2025 earnings, a new institutional whale (AQR 5.09% stake), and the locked October 2026 PDUFA date all confirm the thesis is playing out as mapped.
- 2026-05-06 Buy core UPDATE: Exelixis (EXEL) - Q1 prints another cash-gusher quarter and the Board just stacked another $750M on the buyback pile. Q1 cash generation remains strong, a new $750M buyback authorization compounds the float-shrink thesis, and the PDUFA slip to December 3 is a routine adjustment that does not impair the bridge strategy.
- 2026-06-22 Buy core UPDATE: Exelixis (EXEL) - STELLAR-303 Clears the Second Bar STELLAR-303 no-liver-mets subgroup reportedly hit statistical significance for OS, retiring meaningful clinical risk on the lead asset and strengthening the CRC launch narrative ahead of the December 3 PDUFA.
- 2026-08-06 Speculative buy speculative UPDATE: Exelixis (EXEL) - The Mea Culpa on STELLAR-303 The STELLAR-303 no-liver-mets subgroup actually missed (HR 0.83, P=0.1185) and management trimmed guidance for the first time, weakening the launch narrative; downgrading conviction while the cash floor and ITT approval path remain intact.
- 2026-08-31 Buy core UPDATE: Exelixis (EXEL) - The Wolves Get Pushed Back to 2030 CAFC affirmed the CABOMETYX malate salt patents locking January 15, 2030 exclusivity, removing the largest tail risk to the cash engine and satisfying one of the three stated upgrade conditions.
- 2026-09-11 Speculative buy speculative UPDATE: Exelixis (EXEL) - The Christmas Present Gets Pushed to Spring FDA issued a major amendment extending the PDUFA to March 3, 2027 after requesting updated safety and efficacy data, adding new uncertainty to a launch narrative already weakened by the NLM miss.
- 2026-10-30 Hold UPDATE: Exelixis (EXEL) - The Wolves Found a Side Door Handa received full FDA approval for a cabozantinib capsule via a salt-swap route that bypasses the malate patents, STELLAR-304 slipped to Q1 2027, and the stock is up 18% while the patent picture has weakened — warranting a step down to Hold.
- Long call · opened Jan 30, 2026 at $41.36 · +68.2% vs XBI +22.0% (Nov 6, 2026)
Every verdict Biotech Distilled has published on this company, in order, with the post it came from — the full history, never a selection. Position figures are the same ones shown on /track-record, computed by the same method. Editorial opinion, not investment advice.
Timing, in the company's words (6 quotes from 4 filings)
Sentences quoted verbatim from the company's SEC filings, newest filing first. Each sits under the filing it appeared in; the "matched to" tag names the calendar row it was read for.
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“We expect top-line results in the first quarter of 2027.”
matched to STELLAR-304 · topline data · read as first quarter of 2027 -
“In February 2026, we announced that the FDA had accepted our NDA and assigned a standard review, with a Prescription Drug User Fee Act (PDUFA) target action date of December 3, 2026.”
matched to Zanzalintinib · regulatory decision · read as December 3, 2026
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“In February 2026, we announced that the FDA had accepted our NDA and assigned a standard review, with a Prescription Drug User Fee Act (PDUFA) target action date of December 3, 2026.”
matched to Zanzalintinib · regulatory decision · read as December 3, 2026
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“The FDA assigned a Prescription Drug User Fee Act (PDUFA) target action date of December 3, 2026.”
matched to Zanzalintinib · regulatory decision · read as December 3, 2026
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“The FDA assigned a Prescription Drug User Fee Act (PDUFA) target action date of December 3, 2026.”
matched to Zanzalintinib · regulatory decision · read as December 3, 2026 -
“In February 2026, we announced that the FDA had accepted our NDA and assigned a standard review, with a Prescription Drug User Fee Act (PDUFA) target action date of December 3, 2026.”
matched to Zanzalintinib · topline data · read as December 3, 2026
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Timing sentences quoted from the company's own SEC filings, each under the filing it appeared in. The 'matched to' tag is the calendar row the sentence was read for; the filing is the source. Not investment advice.
Filings & releases (23)
SEC filings from EDGAR and press releases captured from the company's investor-relations site, newest first. Releases captured from May 5, 2026; filings from March 2026. Summaries come from the BD update that read the document; "BD extracted" counts point at the pipeline table above. All companies →
- Nov 3, 2026ReleaseExelixis to Webcast Fireside Chats as Part of Upcoming Investor Conferences in November
- Oct 29, 2026ReleaseExelixis Announces Third Quarter 2026 Financial Results and Provides Corporate Update→ BD updateSummary on the 8-KBD extracted 1 program update from this document → EXEL pipeline
- Oct 29, 20268-KCurrent report: results of operations · EX-99.1→ BD updateQ3 2026 earnings beat with CABOMETYX still printing cash, but STELLAR-304 topline has slipped to Q1 2027 — the RCC displacement leg of the Zanza Switch thesis now won't resolve until next year, alongside the March 3 PDUFA.
- Oct 29, 202610-QQuarterly report→ BD updateSummary on the 8-K
- Oct 15, 2026ReleaseExelixis to Release Third Quarter 2026 Financial Results on Thursday, October 29, 2026
- Sep 11, 20268-KCurrent report: other events→ BD updateThe FDA has extended the zanzalintinib PDUFA by three months to March 3, 2027 — the second slip in this review cycle — after classifying Exelixis' updated safety and efficacy submission as a major amendment, pushing the "Christmas present" binary into Q1 2027.
- Sep 1, 2026ReleaseExelixis to Webcast Fireside Chats as Part of Upcoming Investor Conferences in September
- Aug 31, 2026ReleaseExelixis Announces Update on Patent Litigation Trial Appeal with MSN Laboratories→ BD updateSummary on the 8-K
- Aug 31, 20268-KCurrent report: other events→ BD updateThe Federal Circuit just upheld the three cabozantinib salt patents that define the January 2030 exclusivity floor, removing the appellate-level overhang that was the biggest near-term threat to the Zanza Switch bridge strategy.
- Aug 14, 2026SCHEDULE 13D/A13D amendment
- Aug 5, 2026ReleaseExelixis Announces Second Quarter 2026 Financial Results and Provides Corporate Update
- Aug 5, 20268-KCurrent report: results of operations · EX-99.1BD extracted 2 program updates from this document → EXEL pipeline
- Aug 5, 202610-QQuarterly report
- Jul 22, 2026ReleaseExelixis to Release Second Quarter 2026 Financial Results on Wednesday, August 5, 2026
- Jun 22, 2026ReleaseExelixis Provides Update on the Phase 3 STELLAR-303 Trial Evaluating Zanzalintinib in Combination with an Immune Checkpoint Inhibitor in Patients with Metastatic Colorectal Cancervia aggregator
- May 30, 2026ReleaseExelixis Announces Results from Subgroup Analysis of Phase 3 CABINET Pivotal Trial Evaluating CABOMETYX® (cabozantinib) in Non-Functional and Functional Neuroendocrine Tumors at ASCO 2026via aggregator
- May 29, 20268-KCurrent report: officer / director change, shareholder vote
- May 5, 2026ReleaseExelixis Announces First Quarter 2026 Financial Results and Provides Corporate Update
- May 5, 20268-KCurrent report: results of operations, other events · EX-99.1
- May 5, 202610-QQuarterly report
- Apr 17, 2026DEFA14AProxy soliciting material
- Apr 15, 2026DEFA14AProxy soliciting material
- Apr 15, 2026DEF 14AProxy statement
4 more filings (13G holder notices, S-8, proxy material, SEC correspondence …)
- Aug 12, 2026SCHEDULE 13G/A13G amendment
- Aug 5, 2026S-8Employee plan registration
- Apr 29, 2026SCHEDULE 13GPassive >5% holder (13G)
- Mar 26, 2026SCHEDULE 13G/A13G amendment