Nurix Therapeutics, Inc. (NRIX) SEC Filings & Earnings Calls
EquiReason read 15 Nurix Therapeutics, Inc. SEC filings in the last 12 months. Latest: 10-Q on 2026-10-13 — Nurix entered into a global co-development and co-commercialization collaboration with Roche for bexobrutideg, receiving a $700M upfront payment and eligibility for up to $1.6B in .
Source: SEC EDGAR filings · figures as of 2026-08-31 · read by EquiReason
- Market cap
- 2.8B
- P/E TTM
- 10.0
- Dividend yield
- 0.0%
- 52-week
- —
- Next earnings
- 26 Jan, in 94 days
Every filing, read
last 12 months · SECWhat happened, the numbers inside, guidance and risks. The original is one click away.
13 Oct 202610-QNurix entered into a global co-development and co-commercialization collaboration with Roche for bexobrutideg, receiving a $700M upfront payment and eligibility for up to $1.6B in milestones plus tiered royalties.open
Figures in the filing · each found in the filing text
| Total revenue · Q3-2026 | $673M | +8426% y/y |
| Net income (loss) · Q3-2026 | $550M | -736% y/y |
| Research and development expenses · Q3-2026 | $79M | -8% y/y |
| General and administrative expenses · Q3-2026 | $34M | +161% y/y |
| Operating cash flow · 9M-2026 | $447M | -346% y/y |
Risks flagged
Dependence on Roche collaboration
“Because bexobrutideg is our lead drug candidate, our future prospects depend substantially on the success of the Roche collaboration.” · word for word
Clinical trial failure risk
“The risk of failure for our current lead drug candidates remains high.” · word for word
Need for additional capital
“We will need substantial additional funding to support our continuing operations and pursue our long-term business plan.” · word for word
Manufacturing reliance on single source CMOs
“We rely on third-party contract manufacturing organizations (CMOs) for the manufacture of both drug substance and finished drug product for our drug candidates for preclinical and clinical testing and expect to continue to do so for any future clinical trials and commercialization.”
13 Oct 20268-K · 2.02Nurix reports Q3 2026 results with $1.1B cash, $27M collaboration revenue, and key pipeline progress including Phase 3 start for bexobrutideg and Sanofi milestone.earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · Q3-2026 | $1.10B | |
| Collaboration revenue · Q3-2026 | $27M | |
| Objective response rate (Phase 1a CLL) · CLL/SLL · Phase 1a | 83.0% | |
| Median progression-free survival (Phase 1a CLL) · CLL/SLL · Phase 1a | $22.10 |
Risks flagged
Discontinuation of NX-2127 may indicate pipeline prioritization risk.
“Nurix made the decision to discontinue further clinical development of NX-2127” · word for word
9 Jul 20268-K · 2.02Cash, cash equivalents and marketable securities $444M; Pro-forma cash $1.14B; Objective response rate (ORR) - Phase 1a 83earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · Q2-2026 | $444M | |
| Pro-forma cash · Q2-2026 | $1.14B | |
| Objective response rate (ORR) - Phase 1a · CLL/SLL · Q2-2026 | 83.0% | |
| Median progression-free survival - Phase 1a · CLL/SLL · Q2-2026 | $22.10 | |
| Objective response rate (ORR) - Phase 1b Cohort 5 · CLL/SLL · Q2-2026 | 92.9% | |
| Objective response rate (ORR) - Phase 1b Cohort 15 · CLL/SLL · Q2-2026 | 84.2% |
Risks flagged
Collaboration subject to customary closing conditions including HSR clearance.
“The collaboration agreement is subject to customary closing conditions, including expiration or termination of the applicable waiting period under the Hart-Scott-Rodino Antitrust Improvements Act.” · word for word
9 Jul 202610-QTotal revenue $9M (-79% y/y); Net loss $-90M (+106% y/y); Research and development expenses $88M (+12% y/y)open
Figures in the filing · each found in the filing text
| Total revenue · Q2-2026 | $9M | -79% y/y |
| Net loss · Q2-2026 | $-90M | +106% y/y |
| Research and development expenses · Q2-2026 | $88M | +12% y/y |
| General and administrative expenses · Q2-2026 | $16M | +9% y/y |
| Cash and cash equivalents · 2026-05-31 | $68M | -20% y/y |
| Marketable securities · 2026-05-31 | $376M | +9% y/y |
| Operating cash flow · H1-2026 | $-168M | +36% y/y |
Risks flagged
Cash burn and going concern risk
“The Company does not expect its existing cash, cash equivalents and marketable securities to be sufficient to fund the completion of its clinical trials through commercialization and will need substantial additional funding to support its continuing operations and pursue its long-term business plan.” · word for word
Collaboration revenue dependency
“Total revenue $ 9,043 $ 44,056 (79) %”
8 Apr 20268-K · 2.02Revenue $6M (-66% y/y); Net loss $-87M (+55% y/y); Research and development expenses $84M (+21% y/y)earningsopen
Figures in the filing · each found in the filing text
| Revenue · Q1-2026 | $6M | -66% y/y |
| Net loss · Q1-2026 | $-87M | +55% y/y |
| Research and development expenses · Q1-2026 | $84M | +21% y/y |
| General and administrative expenses · Q1-2026 | $15M | +25% y/y |
| Cash and cash equivalents · Q1-2026 | $541M |
Risks flagged
Revenue decline due to collaboration end; net loss widening; high cash burn rate.
“Revenue decreased from $18.5M to $6.3M; net loss increased from $56.4M to $87.2M.”
8 Apr 202610-QNurix reported a net loss of $87.2M for Q1 2026, wider than the $56.4M loss in Q1 2025, driven by a 66% decline in collaboration revenue and a 21% increase in R&D expenses.earningsopen
Figures in the filing · each found in the filing text
| Collaboration revenue · Q1-2026 | $6M | -66% y/y |
| Net loss · Q1-2026 | $-87M | +55% y/y |
| Research and development expenses · Q1-2026 | $84M | +21% y/y |
| General and administrative expenses · Q1-2026 | $15M | +25% y/y |
| Cash, cash equivalents and marketable securities · 2026-02-28 | $541M |
Risks flagged
Clinical trial failure risk
“Our lead drug candidates, bexobrutideg (NX-5948), zelebrudomide (NX-2127) and NX-1607, are in the early stages of clinical development and their risk of failure is high.” · word for word
Need for additional capital
“We will need substantial additional funding to support our continuing operations and pursue our long-term business plan.” · word for word
Dependence on collaborations
“We expect to depend on collaborations with third parties for the research, development and commercialization of certain of the drug candidates we may develop.” · word for word
Manufacturing and supply chain risk
“We rely on third-party contract manufacturing organizations (CMOs) for the manufacture of both drug substance and finished drug product for our drug candidates for preclinical and clinical testing and expect to continue to do so for any future clinical trials and commercialization.” · word for word
Intellectual property risk
“If we are unable to obtain and maintain patent protection for our technology, our current drug candidates and any future drug candidates that we may develop, or if the scope of the patent protection obtained is not sufficiently broad, our competitors and other third parties could develop and commercialize technology and drug candidates similar or identical t” · word for word
27 Mar 2026DEF 14AAnnual proxy statement filed; no material event disclosed beyond standard executive compensation and governance matters.open
Figures in the filing · each found in the filing text
| Cash, cash equivalents, and marketable securities · FY2025 | $593M | |
| Collaboration revenue · FY2025 | $84M | |
| Objective response rate (ORR) - bexobrutideg Phase 1a CLL · bexobrutideg · 2025 | 83.0% | |
| Median progression-free survival - bexobrutideg Phase 1a CLL · bexobrutideg · 2025 | $22.10 | |
| Median duration of response - bexobrutideg Phase 1a CLL · bexobrutideg · 2025 | $20.10 | |
| Objective response rate (ORR) - bexobrutideg Phase 1 WM · bexobrutideg · 2025 | 75.0% | |
| Disease control rate - NX-1607 · NX-1607 · 2025 | 49.3% | |
| Potential future milestones and royalties · 2025 | $6.10B | |
| Net loss · FY2025 | $-264M |
Risks flagged
Clinical trial failure risk
“whether Nurix will be able to advance its drug candidates, obtain regulatory approval of and ultimately commercialize its drug candidates” · word for word
Financing risk
“whether Nurix will be able to fund development activities and achieve development goals” · word for word
Competition risk
“other risks and uncertainties described under the heading 'Risk Factors' in Nurix's Annual Report on Form 10-K” · word for word
6 Mar 20268-K · 8.01At-the-market offering capacity $414Mopen
Figures in the filing · each found in the filing text
| At-the-market offering capacity · Q1-2026 | $414M |
Risks flagged
Significant potential dilution from ATM program.
“Up to $413.65M in shares may be sold; dilutive to existing shareholders.”
28 Jan 20268-K · 2.02Cash and marketable securities $593M; Objective response rate (ORR) 83; Median progression-free survival (PFS) 22.1earningsopen
Figures in the filing · each found in the filing text
| Cash and marketable securities · Q4-2025 | $593M | |
| Objective response rate (ORR) · bexobrutideg CLL · Q4-2025 | 83.0% | |
| Median progression-free survival (PFS) · bexobrutideg CLL · Q4-2025 | $22.10 | |
| Median duration of response · bexobrutideg CLL · Q4-2025 | $20.10 |
Risks flagged
Clinical-stage biotech with no approved products; regulatory and commercial risks remain high.
“clinical-stage biopharmaceutical company” · word for word
28 Jan 202610-KObjective Response Rate (ORR) in CLL Phase 1a 83; Median Progression Free Survival (PFS) in CLL Phase 1a 22.1; Total Collaboration Funding Received $482Mopen
Figures in the filing · each found in the filing text
| Objective Response Rate (ORR) in CLL Phase 1a · CLL · FY2025 | 83.0% | |
| Median Progression Free Survival (PFS) in CLL Phase 1a · CLL · FY2025 | $22.10 | |
| Total Collaboration Funding Received · FY2025 | $482M |
Risks flagged
Early-stage pipeline risk
“We are early in our development efforts. Our lead drug candidates... are in the early stages of clinical development.” · word for word
Funding dependency
“We will need substantial additional funding. If we are unable to raise capital when needed, we may be required to delay, limit, reduce or terminate our research or product development programs.” · word for word
12 Jan 20268-K · 7.01Objective response rate 83; Median progression-free survival 22.1open
Figures in the filing · each found in the filing text
| Objective response rate · CLL · 2025 | 83.0% | |
| Median progression-free survival · CLL · 2025 | $22.10 |
9 Dec 20258-K · 7.01, 8.01Objective Response Rate (ORR) 83; Median Progression-Free Survival (PFS) 22.1; Disease Control Rate (DCR) 95.7open
Figures in the filing · each found in the filing text
| Objective Response Rate (ORR) · CLL/SLL · Q4-2025 | 83.0% | |
| Median Progression-Free Survival (PFS) · CLL/SLL · Q4-2025 | $22.10 | |
| Disease Control Rate (DCR) · CLL/SLL · Q4-2025 | 95.7% |
Risks flagged
Clinical trial risk remains; Phase 2 enrollment and regulatory approval are uncertain.
“Phase 2 clinical trial of bexobrutideg (DAYBreak-CLL-201) currently enrolling globally” · word for word
Nurix Therapeutics, Inc. — questions
- What did Nurix Therapeutics, Inc. file recently?
- 15 SEC filings in the last 12 months. Latest: 10-Q on 2026-10-13 — Nurix entered into a global co-development and co-commercialization collaboration with Roche for bexobrutideg, receiving a $700M upfront payment and eligibility for up to $1.6B in milestones plus tiered royalties.
Every figure on this page comes from Nurix Therapeutics, Inc.'s own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.
How these figures are read: methodology · EquiReason.