Nurix Therapeutics
NRIXNASDAQUSD
- — Source valuation snapshot. Not a live recalculation.
- — Latest filed annual earnings; price snapshot date unavailable. Not forward P/E.
- — Diluted earnings per share from the latest filed annual.
- $16.14 Prior regular-session close from the quote source.
- $15.75–$16.76 Regular-session low and high so far today.
- 3.0M Regular-session shares traded · Nov 10, 4:00 PM ET.
- Jan 27 projected Projected for 2027-01-27 from the company’s own results filings (SEC 8-K Item 2.02). The company has not confirmed the date.
- $12.01–$28.23 52-week trading low and high returned by the quote source.
Understand the Business
Why the Stock Moved
Period-matched expectations history is not yet available. Current metrics are not a substitute for a historical explanation.
The core investment thesis
Own NRIX if Nurix’s DEL-AI discovery engine plus ligase expertise can turn hard-to-drug targets into a broad, partner-funded pipeline of first-in-class targeted protein degraders where a successful pivotal for bexobrutideg would validate the platform and drive large.
NRIX price history
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INVESTMENT THESIS
What must happen next
Nurix’s DEL-AI discovery engine will continue to generate partner-funded discovery and milestone revenue because its DEL data and ML models enable prospectively identifying binders for diverse, pharmaceutically relevant targets.StrengtheningMateriality: High
Revenue increased to $83.98M in FY2025 from $54.55M in FY2024 and $76.99M in FY2023 (shows commercial/partner receipts exist and can grow). If true, recurring collaboration revenue and milestone realizations will fund development, validate the platform commercially, and reduce dilution; if false, partner interest and revenue will fade and valuation will collapse.
Watch: Large pharmas replicate or insource TPD discovery (reducing external demand) or preferentially develop discovery internally.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Revenue increased to $83.98M in FY2025 from $54.55M in FY2024 and $76.99M in FY2023 (shows commercial/partner receipts exist and can.
Open source ↗Bexobrutideg’s Phase 2 results and subsequent FDA interactions are the single largest value inflection: positive, registrational-quality efficacy and acceptable safety will unlock commercial sales and large downstream milestones/royalties; negative or non-pivotal results will remove the main near-term value driver.HoldingMateriality: High
Bexobrutideg Phase 2 study commenced October 2025 and was agreed with the FDA to use the 600 mg once-daily dose (MD&A/Business: regulatory engagement and Fast Track/PRIME designations). A strong Phase 2 (and an accelerated approval path) would validate Nurix’s approach, attract partners/customers, and justify the current valuation; failure would leave the company reliant on preclinical discovery monetization and likely force repricing.
Watch: Clinical setbacks such as safety signals or insufficient efficacy in Phase 2, or an FDA determination that Phase 2 data are inadequate for accelerated approval.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Bexobrutideg Phase 2 study commenced October 2025 and was agreed with the FDA to use the 600 mg once-daily dose.
Open source ↗Large pharma collaborations materially de-risk Nurix’s development program because they supply non-dilutive cash, milestone upside, and optional co-development economics that can fund pipeline advancement without equity raises.HoldingMateriality: Medium
Cash and cash equivalents rose to $246.96M as of Nov 30, 2025 (balance-sheet strength vs prior years). If partnerships continue delivering milestones/cash, Nurix can fund operations and advance multiple programs; if partners stop paying or opt out, the company faces financing pressure and dilution.
Watch: Partners delay or terminate programs (e.g., Gilead, Sanofi, Pfizer stop advancing or decide against milestone-triggering development), removing expected payments.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Cash and cash equivalents rose to $246.96M as of Nov 30, 2025 (balance-sheet strength vs prior years).
Open source ↗At current operating cash burn, Nurix will exhaust its cash runway within roughly one year unless it receives material partner milestone payments or raises capital.StrengtheningMateriality: Medium
Operating cash flow was -$249,465,000 for FY2025 (company is burning ~ $250M per year). If cash is consumed without milestone receipts or capital, the company will need to raise funds (likely dilutive) or cut programs, both of which would materially lower equity value.
Watch: Imminent, large milestone or licensing payments from collaborators that materially improve cash balance.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Operating cash flow was -$249,465,000 for FY2025 (company is burning ~ $250M per year).
Open source ↗If Nurix repeatedly translates DEL-AI hits into clinic-stage candidates, the cumulative DEL data, ML models and ligase expertise will form a durable moat that sustains collaboration flow and optionality for co-development/co-commercialization.HoldingMateriality: Medium
Total assets increased to $688.135M as of Nov 30, 2025 from $355.598M in FY2023 — consistent with heavy investment in platform, IP and pipeline. A reproducible discovery → clinic pipeline would justify premium valuation and recurring high-value partnerships; if the platform cannot scale to multiple clinical successes, the moat will not exist and partner interest will fade.
Watch: Multiple clinical candidates fail to show translational signal (e.g., lack of target engagement or efficacy in clinic) demonstrating the discovery outputs do not scale.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Total assets increased to $688.135M as of Nov 30, 2025 from $355.598M in FY2023 — consistent with heavy investment in.
Open source ↗
Full investment case & evidence
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Original research
Nurix’s DEL-AI discovery engine will continue to generate partner-funded discovery and milestone revenue because its DEL data and ML models enable prospectively identifying binders for diverse, pharmaceutically relevant targets. If true, recurring collaboration revenue and milestone realizations will fund development, validate the platform commercially, and reduce dilution; if false, partner interest and revenue will fade and valuation will collapse.
Bexobrutideg’s Phase 2 results and subsequent FDA interactions are the single largest value inflection: positive, registrational-quality efficacy and acceptable safety will unlock commercial sales and large downstream milestones/royalties; negative or non-pivotal results will remove the main near-term value driver. A strong Phase 2 (and an accelerated approval path) would validate Nurix’s approach, attract partners/customers, and justify the current valuation; failure would leave the company reliant on preclinical discovery monetization and likely force repricing.
Large pharma collaborations materially de-risk Nurix’s development program because they supply non-dilutive cash, milestone upside, and optional co-development economics that can fund pipeline advancement without equity raises. If partnerships continue delivering milestones/cash, Nurix can fund operations and advance multiple programs; if partners stop paying or opt out, the company faces financing pressure and dilution.
At current operating cash burn, Nurix will exhaust its cash runway within roughly one year unless it receives material partner milestone payments or raises capital. If cash is consumed without milestone receipts or capital, the company will need to raise funds (likely dilutive) or cut programs, both of which would materially lower equity value.
If Nurix repeatedly translates DEL-AI hits into clinic-stage candidates, the cumulative DEL data, ML models and ligase expertise will form a durable moat that sustains collaboration flow and optionality for co-development/co-commercialization. A reproducible discovery → clinic pipeline would justify premium valuation and recurring high-value partnerships; if the platform cannot scale to multiple clinical successes, the moat will not exist and partner interest will fade.
All standing thesis claims
Original report summary
Nurix’s DEL-AI discovery engine plus ligase expertise can turn hard-to-drug targets into a broad, partner-funded pipeline of first-in-class targeted protein degraders where a successful pivotal for bexobrutideg would validate the platform and drive large.
BULL CASE / BEAR CASE
Bull case and bear case for Nurix Therapeutics
Where the evidence on Nurix Therapeutics stands: Holding on the latest evidence (Nov 9, 2026). Of its 5 thesis points, 2 strengthening and 3 holding.
Bull case: what the evidence supports
Nurix’s DEL-AI discovery engine will continue to generate partner-funded discovery and milestone revenue because its DEL data and ML models enable prospectively identifying binders for diverse, pharmaceutically relevant targets.
Bexobrutideg’s Phase 2 results and subsequent FDA interactions are the single largest value inflection: positive, registrational-quality efficacy and acceptable safety will unlock commercial sales and large downstream milestones/royalties; negative or non-pivotal results will remove the main near-term value driver.
Large pharma collaborations materially de-risk Nurix’s development program because they supply non-dilutive cash, milestone upside, and optional co-development economics that can fund pipeline advancement without equity raises.
At current operating cash burn, Nurix will exhaust its cash runway within roughly one year unless it receives material partner milestone payments or raises capital.
If Nurix repeatedly translates DEL-AI hits into clinic-stage candidates, the cumulative DEL data, ML models and ligase expertise will form a durable moat that sustains collaboration flow and optionality for co-development/co-commercialization.
Bear case: what would count against it
Large pharmas replicate or insource TPD discovery (reducing external demand) or preferentially develop discovery internally.
Clinical setbacks such as safety signals or insufficient efficacy in Phase 2, or an FDA determination that Phase 2 data are inadequate for accelerated approval.
Partners delay or terminate programs (e.g., Gilead, Sanofi, Pfizer stop advancing or decide against milestone-triggering development), removing expected payments.
Thesis-Break Engine
Thesis-break watch · Nurix Therapeutics
No break has crossed Nurix Therapeutics’s thesis. Its break conditions are checked against every new filing as it lands.
MARKET + FINANCIAL SNAPSHOT
The numbers behind the thesis
What Changed
- MIXEDOther material event.
Nurix Therapeutics filed an SEC 8-K on 2026-11-03: Other material event. It is a dated development that tests the current thesis.
- MIXEDReported results of operations (earnings release).
Nurix Therapeutics filed an SEC 8-K on 2026-10-13: Reported results of operations (earnings release). It is a dated development that tests the current thesis.
- MIXEDReported results of operations (earnings release).
Nurix Therapeutics filed an SEC 8-K on 2026-07-09: Reported results of operations (earnings release). It is a dated development that tests the current thesis.
RISKS / FALSIFIERS
What could break the thesis
- Large pharmas replicate or insource TPD discovery (reducing external demand) or preferentially develop discovery internally.
- Clinical setbacks such as safety signals or insufficient efficacy in Phase 2, or an FDA determination that Phase 2 data are inadequate for accelerated approval.
- Partners delay or terminate programs (e.g., Gilead, Sanofi, Pfizer stop advancing or decide against milestone-triggering development), removing expected payments.
- Imminent, large milestone or licensing payments from collaborators that materially improve cash balance.
- Multiple clinical candidates fail to show translational signal (e.g., lack of target engagement or efficacy in clinic) demonstrating the discovery outputs do not scale.
NRIX news
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FINANCIAL STATEMENTS
NRIX income statement
Annual filed results · USD · Oldest to newest. Margins are calculated from the reported figures.
NRIX: quick answers
- When does Nurix Therapeutics (NRIX) report earnings next?
- Nurix Therapeutics's next results are projected for January 27, 2027, from the dates of its own results filings with the SEC. The company has not confirmed the date. It last reported on October 13, 2026. Earnings calendar
- What is NRIX's short interest?
- As of October 30, 2026, 18.9M NRIX shares were sold short, down 8.1% from the count before. At the stock's average daily volume that is 7.2 days to cover. FINRA publishes the count twice a month. NRIX short interest history
- Have members of Congress traded NRIX?
- 1 trade in NRIX has been disclosed under the STOCK Act by members of Congress, the President or senior officials, none in reports made public in the last 90 days. Every disclosed NRIX trade
- Which well-known investors own NRIX?
- 1 of the 37 well-known funds tracked here reported NRIX shares in their latest 13F filing. By share of the fund's portfolio: ARK Investment Management (Cathie Wood), 0.3%. Fund portfolios
NRIX in well-known investors’ portfolios
1 of 37 funds reported NRIX shares in their latest 13F filing. A 13F shows quarter-end positions and arrives up to 45 days later.
| Fund | Of its portfolio | Value | Change | Quarter |
|---|---|---|---|---|
| Cathie WoodARK Investment Management | 0.28% | $43.5M | +4.2% | Q2 2026 |
