Syndax Pharmaceuticals, Inc. (SNDX) Stock Price & How to Invest
Last updated July 2026
Short answer
Syndax Pharmaceuticals is a commercial-stage oncology company based in New York with two FDA-approved medicines: Revuforj (revumenib), the first menin inhibitor ever approved, and Niktimvo (axatilimab-csfr), a CSF-1R blocking antibody for chronic graft-versus-host disease. The structural thing a screener gets wrong here is that only one of those two drugs reaches the revenue line as product sales. Incyte is the principal on every Niktimvo sale and books all of it, so Syndax records only its 50% share of net commercial profit as collaboration revenue, which is why ~$252M of trailing revenue sits underneath roughly $400M of combined branded sales the two medicines actually generated. A separate $350M Royalty Pharma financing takes 13.8% off US Niktimvo net sales, and that cost lands in interest expense rather than in revenue or cost of goods.
SNDX stock price
As of 2026-08-21, Syndax Pharmaceuticals, Inc. (SNDX) last closed at $19.65, up 21.0% over the past year. Over the past 52 weeks it has traded between $13.11 and $25.15.
Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or Syndax Pharmaceuticals, Inc.'s investor relations page. Walnut is informational, not investment advice.
What does Syndax Pharmaceuticals, Inc. (SNDX) do?
Syndax Pharmaceuticals (Nasdaq: SNDX) sells two approved medicines and funds a pipeline behind them. Revuforj (revumenib) is an oral menin inhibitor, approved by the FDA on November 15, 2024 for relapsed or refractory acute leukemia carrying a KMT2A translocation in patients one year and older, then expanded on October 24, 2025 into relapsed or refractory AML with a susceptible NPM1 mutation. Syndax owns it outright in the US, licensed originally from Vitae Pharmaceuticals, now an AbbVie subsidiary, and books its sales as product revenue. Niktimvo (axatilimab-csfr) is a first-in-class antibody against the CSF-1 receptor, approved in August 2024 for chronic graft-versus-host disease after at least two prior lines of systemic therapy in patients weighing 40kg or more. It was in-licensed from UCB Biopharma in 2016 and then partnered with Incyte in September 2021 under a worldwide co-development and co-commercialization agreement. Incyte runs the commercial engine and records the sales; Syndax takes half the net commercial profit. In the second quarter of 2026 Revuforj generated $54.7M of net product revenue on roughly 1,500 prescriptions, while Niktimvo generated $60.3M of net sales at Incyte, of which $18.1M reached Syndax. The company employed about 298 people at last count.
The financial picture is a launch curve running into a fixed cost base. Total revenue went from $23.7M in 2024 to $172.4M in 2025 to ~$252M for the twelve months to June 30, 2026, and the second quarter alone was $72.8M, up 92% year over year. Operating expenses barely moved over that stretch: total opex was $211.8M for the first half of 2026 against $210.9M a year earlier, and management has guided full-year R&D plus SG&A to approximately $400M excluding roughly $50M of non-cash stock compensation, down from $438.5M in 2025. Operating loss narrowed accordingly, from $153.1M in the first half of 2025 to $74.2M in the first half of 2026. What the market is paying for sits mostly outside those numbers. Revuforj and Niktimvo are both approved only in later-line settings, and the pivotal trials that would move revumenib into newly diagnosed AML (EVOLVE-2 and REVEAL-ND) and axatilimab into frontline cGVHD and idiopathic pulmonary fibrosis are still reading out. At ~$19.65 a share the equity is capitalised around $1.75B, with $575.1M of cash against $688.6M of total liabilities.
What's driving Syndax Pharmaceuticals, Inc. (SNDX)?
1. Revuforj moving from KMT2A into the far larger NPM1 population
The original November 2024 approval covered KMT2A-rearranged acute leukemia, a genuinely rare subset. The October 24, 2025 label expansion added relapsed or refractory AML with a susceptible NPM1 mutation, which is roughly a third of adult AML and several times the size of the first indication. The revenue trace since then shows the effect: $44.2M in the fourth quarter of 2025, $48.9M in the first quarter of 2026, and $54.7M in the second, with prescriptions of about 1,500 in the latest quarter, up 121% year over year. Management describes a sixth consecutive quarter of double-digit net revenue and prescription growth, and attributes part of it to longer average treatment duration as more patients stay on drug in the post-transplant setting.
2. Niktimvo, where Syndax sees half the profit and none of the sales line
Incyte booked $60.3M of Niktimvo net sales in the second quarter of 2026, up 67% year over year and 9% sequentially, from $151.6M across all of 2025. Syndax's reported figure was $18.1M, because the agreement splits net commercial profit (net product revenue minus cost of sales and commercial expenses) rather than revenue. Two consequences follow. Syndax's line is inherently lumpier than the drug's own trajectory, since a quarter of heavier commercial investment by Incyte compresses the profit share even while sales grow. And a screener computing gross margin or price-to-sales on Syndax will be working from a number that has already had manufacturing and selling costs deducted from half the franchise.
3. Frontline AML, which is what the valuation is actually about
Every approved use of Revuforj today is in relapsed or refractory disease, where patients are few and treatment durations are short. The company has two pivotal Phase 3 trials aimed at newly diagnosed patients: EVOLVE-2, testing revumenib with venetoclax and azacitidine in NPM1-mutated and KMT2A-rearranged AML patients unfit for intensive chemotherapy, run with the HOVON network, and REVEAL-ND, testing revumenib with intensive chemotherapy in newly diagnosed NPM1-mutated AML. Supporting investigator-led work has been encouraging, including a Journal of Clinical Oncology publication in June 2026 from the Phase 1/2 SAVE trial reporting an 88% overall response rate and 71% composite complete remission in 42 heavily pretreated patients. Whether that translates into a registrational frontline result is the difference between a couple of hundred million in annual sales and something much larger.
4. Expenses flat while revenue triples
Syndax spent $438.5M on R&D and SG&A in 2025 building out two simultaneous launches. The 2026 guide is approximately $400M excluding around $50M of estimated non-cash stock compensation, so the absolute spend is coming down while revenue rises. Second-quarter SG&A fell to $41.5M from $43.8M as the 2025 launch costs did not repeat, and R&D rose only to $68.0M from $62.2M despite the frontline trial expansion. Cash used in operating activities dropped from $183.0M in the first half of 2025 to $80.6M in the first half of 2026. Management states it expects existing cash plus product, collaboration and interest income to carry the company to profitability, though no date is attached to that.
What are the risks to Syndax Pharmaceuticals, Inc. (SNDX)?
Revuforj no longer has the menin inhibitor class to itself. Kura Oncology and Kyowa Kirin won FDA approval for ziftomenib (Komzifti) in November 2025 in relapsed or refractory NPM1-mutated AML, the same population Syndax entered three weeks earlier, and began selling on November 21, 2025. Komzifti is dosed once daily. Both labels carry boxed warnings, including differentiation syndrome and QTc prolongation, so the competition is likely to be fought on dosing convenience, payer access and combination data rather than on a clean safety separation. Kura's partner paid $330M upfront with up to $1.1B in milestones, which funds a serious commercial effort against a Syndax field force that is already carrying two products. The balance sheet is the second issue. Total stockholders' equity was $15.1M at June 30, 2026 against $688.6M of liabilities, and the accumulated deficit stands at $1.6B. The financing is unusual in shape: a $350M upfront from Royalty Pharma in November 2024 that sells 13.8% of US Niktimvo net sales with aggregate payments capped at $822.5M, accounted for as debt, plus $250M of 2.25% convertible senior notes due June 2031 issued in June 2026 at a conversion price near $24.76. Royalty interest expense alone was $12.1M in the second quarter and $24.0M for the half, and it grows as Niktimvo grows. If Niktimvo performs, Syndax pays back up to 2.35 times what it received. The converts add about 10.1M potential shares against 89.4M outstanding. Beyond that, revenue depends on two products in narrow later-line indications, both under UCB and AbbVie-related royalty obligations, with the frontline expansions still unproven. The first quarter of 2026 already showed how sensitive the line is to the January payer reset, falling to $64.9M from $68.7M in the fourth quarter of 2025 despite underlying demand growth.
What is the Syndax Pharmaceuticals, Inc. (SNDX) forecast?
11 analysts publish price targets on SNDX, averaging $37.55 against a $19.65 price as of August 2026, or +91.1%. The published targets run from $26.00 to $57.00, a wide spread, and the ratings split 12 buy, 0 hold, 0 sell. Over the last six months there have been 4 raises and 5 cuts among the published actions. A price target is what an analyst published on a date, not a prediction, and sell-side ratings skew positive across the whole market.
Read the full SNDX forecast and price target for the target table, the recent rating actions by firm, and how the consensus has shifted.
Is SNDX a buy or a sell?
We give no verdict on Syndax Pharmaceuticals, Inc.. Both cases are real, which is why the question is contested at all, so here is the strongest version of each.
The case for buying. Revuforj moving from KMT2A into the far larger NPM1 population. The original November 2024 approval covered KMT2A-rearranged acute leukemia, a genuinely rare subset. The most optimistic published target, $57.00, assumes this works close to its best case.
The case against. Revuforj no longer has the menin inhibitor class to itself. The most pessimistic target, $26.00, is roughly what SNDX is worth if this bites instead.
Read the full bull and bear case on SNDX, including what would have to change to break either one. Walnut is not an investment adviser.
How is Syndax Pharmaceuticals, Inc. (SNDX) valued? (approximate, August 2026)
A simple financial snapshot. These are approximations and refresh quarterly; for current figures see Syndax Pharmaceuticals, Inc.'s investor relations page or your broker.
- Revenue (TTM): ~$252.3M for the twelve months to June 30, 2026, against $172.4M in fiscal 2025 and $23.7M in fiscal 2024. The quarterly path was $68.7M in 4Q25, $64.9M in 1Q26 (a sequential dip driven by the January payer and gross-to-net reset, not by demand) and $72.8M in 2Q26, the last of which was up 92% year over year.
- Product mix (the line that misleads screeners): Of 2Q26's $72.8M, $54.7M was Revuforj net product revenue and $18.1M was collaboration revenue representing Syndax's 50% share of Niktimvo net commercial profit. Incyte separately reported $60.3M of Niktimvo net sales in the quarter. Combined branded sales of the two medicines were therefore ~$115.0M in 2Q26 and over $275M across full-year 2025 ($124.8M Revuforj plus $151.6M Niktimvo), well above the reported revenue line.
- Earnings and EPS: Net loss of $49.4M, or $0.55 per share, in 2Q26 versus $71.8M and $0.83 a year earlier; $92.0M and $1.04 per share for the first half of 2026 versus $156.7M and $1.82. Full-year 2025 net loss was $285.4M and 2024 was $318.8M. Operating loss narrowed to $40.0M in 2Q26 from $69.4M. There is no P/E, and there has never been an annual profit.
- Operating expenses and guidance: 2Q26 R&D was $68.0M (from $62.2M), SG&A $41.5M (from $43.8M) and cost of product sales $3.2M, for $112.8M of total opex. First-half opex was $211.8M against $210.9M a year earlier, so spend is roughly flat while revenue grew 138%. Guidance for full-year 2026 is approximately $400M of R&D plus SG&A excluding ~$50M of estimated non-cash stock compensation, down from $438.5M actual in 2025.
- Cash flow and balance sheet: Cash, cash equivalents and short and long-term investments of $575.1M at June 30, 2026, up from $394.1M at December 31, 2025 after the $250M convertible issue. Operating cash burn fell to $80.6M in the first half of 2026 from $183.0M a year earlier. Total assets $703.7M, total liabilities $688.6M (including a $344.0M royalty interest financing liability and a $244.1M convertible note liability) and stockholders' equity of just $15.1M. Accumulated deficit ~$1.6B.
- Market pricing: ~$19.65 a share in August 2026 for a market capitalisation of ~$1.75B, against a 52-week range of $12.99 to $25.59. Roughly 89.2M common shares outstanding (89.4M including pre-funded warrants), rising to ~116.3M fully diluted once options, RSUs and the 10.1M convertible conversion shares are counted. Those figures work out to ~6.9x trailing sales and roughly 7x EV/sales adjusting for cash and the two debt-like instruments. No dividend, no P/E, beta ~0.37.
Seven times sales is not a demanding multiple for a biotech growing revenue at triple digits, and the reason it is not higher is visible in the structure rather than the growth rate. Half the franchise arrives as a profit share, the Royalty Pharma instrument skims 13.8% of US Niktimvo sales before anything reaches Syndax, and both drugs are approved only in later-line settings where the patient pool is finite. Twelve covering analysts carried a mean target near $37.55 in August 2026, which is a frontline-expansion number rather than a run-rate one.
Who competes with Syndax Pharmaceuticals, Inc. (SNDX)?
Menin inhibitors and targeted AML therapy
The direct rival is ziftomenib (Komzifti) from Kura Oncology and Kyowa Kirin, approved in November 2025 for relapsed or refractory NPM1-mutated AML and dosed once daily against Revuforj's twice-daily regimen. Johnson & Johnson has bleximenib in clinical development, so the class is likely to get more crowded. Beyond menin, Revuforj competes for the same treatment slot with AbbVie and Genentech's venetoclax (Venclexta), which it is also being combined with, Astellas's gilteritinib (Xospata) in FLT3-mutated disease, Servier's ivosidenib (Tibsovo) and Daiichi Sankyo's quizartinib (Vanflyta). Genotype determines much of the competitive overlap, since these agents target different mutations within the same disease.
Chronic GVHD and fibrotic disease
Niktimvo's position in cGVHD is third-line and after, so the incumbents ahead of it are Incyte's own ruxolitinib (Jakafi), Sanofi's belumosudil (Rezurock) and ibrutinib (Imbruvica) from AbbVie and Johnson & Johnson. Incyte is therefore both the partner booking Niktimvo's sales and the owner of the frontline standard the drug is being tested on top of, which is an unusual alignment. The Phase 2 combination with ruxolitinib in newly diagnosed patients reads out in the fourth quarter of 2026. If the parallel Phase 2 in idiopathic pulmonary fibrosis also reads out well, the comparison set widens to Boehringer Ingelheim's nintedanib (Ofev) and Roche's pirfenidone (Esbriet).
Commercial-stage oncology mid-caps competing for capital
For an investor screening the sector, SNDX sits alongside other recently commercial oncology companies of similar size where the multiple is set by launch trajectory rather than earnings: Kura Oncology, Nuvalent, Day One Biopharmaceuticals and Rigel Pharmaceuticals among them. What separates Syndax within that group is that it already has two approved products and a meaningful revenue base, and that it has funded itself through royalty monetisation and convertible debt rather than repeated equity issuance. Share count grew only from 87.4M to 89.2M over the eighteen months to June 2026, which is unusual for a company of this profile.
What stocks are similar to Syndax Pharmaceuticals, Inc. (SNDX)?
Other names that sit close to SNDX: same theme, named as a direct competitor, or held beside it in the same funds. Each entry says which. Worth a look if you are thinking about diversification within a thesis rather than concentration on one ticker.
How to invest in Syndax Pharmaceuticals, Inc. (SNDX)
There are three common ways to get SNDX exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it, which spreads the position across many companies. Or build it into a focused thematic portfolio, so SNDX sits alongside other stocks that express the same thesis.
Walnut takes the portfolio route. Describe a thesis where SNDX fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.
New to this? Start with how to invest in stocks, see how to analyze a stock with AI, or compare the best AI stock analyzers.
The bottom line on Syndax Pharmaceuticals, Inc. (SNDX)
As of August 2026, SNDX is a two-product commercial launch story priced at roughly seven times trailing revenue, where the reported top line understates the drugs by design and the capital structure, not the share count, carries most of the financing. The valuation is mostly a bet on moving revumenib from relapsed disease into frontline AML.
More on Syndax Pharmaceuticals, Inc. (SNDX)
Whether SNDX is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is SNDX a buy or a sell?, and where the stock could go from here in the SNDX stock forecast.
For income investors, whether SNDX pays a dividend and how the payout looks is covered in does SNDX pay a dividend? And to weigh SNDX against a peer, read the full side-by-side comparisons: SNDX vs JNJ and SNDX vs ABBV.
Wondering how SNDX fits the portfolio you already own? Walnut is an AI investing app that connects your brokerage read-only and answers questions like that about your actual holdings: overlap, concentration, and how each position tracks the S&P 500. Compare the best AI portfolio analyzers or see the best AI investing apps in 2026.
Investing in Syndax Pharmaceuticals, Inc. with AI
Connect the broker you already use and ask Walnut's AI how SNDX fits what you actually hold: whether you own it already through a fund, what it would do to your concentration, and how it has tracked the S&P 500. Read-only by default, and you approve anything before it reaches your broker.
FAQ
What does Syndax Pharmaceuticals do?
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Syndax is a commercial-stage biopharmaceutical company headquartered in New York that develops and sells cancer and immune-mediated disease therapies. It has two FDA-approved medicines. Revuforj (revumenib) is an oral menin inhibitor approved in November 2024 for relapsed or refractory acute leukemia with a KMT2A translocation and expanded in October 2025 into relapsed or refractory AML with a susceptible NPM1 mutation. Niktimvo (axatilimab-csfr) is an antibody blocking the CSF-1 receptor, approved in August 2024 for chronic graft-versus-host disease after at least two prior lines of systemic therapy. Behind those, Syndax is running Phase 3 trials to move revumenib into newly diagnosed AML and testing axatilimab in frontline cGVHD and idiopathic pulmonary fibrosis. Two earlier-stage programmes, an allosteric EGFR inhibitor for lung cancer and a next-generation menin inhibitor for myelofibrosis, are targeted for INDs in 2027.
Why is SNDX revenue lower than its drug sales?
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Because only one of the two drugs flows through as product revenue. Syndax partnered axatilimab with Incyte in September 2021, and under accounting rules for collaboration arrangements Incyte is the principal in product sales. Incyte therefore records all Niktimvo revenue, and Syndax records only its 50% share of net commercial profit, defined as net product revenue minus cost of sales and commercial expenses. In the second quarter of 2026 that meant $60.3M of Niktimvo sales at Incyte produced $18.1M of collaboration revenue at Syndax. Revuforj, which Syndax owns outright in the US, is recorded gross at $54.7M in the same quarter. Anyone computing price-to-sales or gross margin from the reported top line is mixing a gross number with a net-of-costs profit share, which makes both ratios non-comparable to a conventional specialty pharmaceutical company.
Is SNDX profitable?
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No. Syndax reported a net loss of $49.4M, or $0.55 per share, in the second quarter of 2026, and $92.0M for the first half. Full-year 2025 was a $285.4M loss and 2024 was $318.8M. The trend is improving quickly: the operating loss narrowed from $153.1M in the first half of 2025 to $74.2M in the first half of 2026, because revenue more than doubled while total operating expenses stayed essentially flat at around $212M. Operating cash burn fell from $183.0M to $80.6M over the same comparison. Management has said it expects existing cash together with product revenue, collaboration revenue and interest income to carry the company to profitability, but no target date has been given and the accumulated deficit stands at roughly $1.6B.
Who are SNDX's competitors?
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In menin inhibition, the direct competitor is ziftomenib (Komzifti) from Kura Oncology and Kyowa Kirin, approved in November 2025 for the same relapsed or refractory NPM1-mutated AML population Revuforj entered three weeks earlier. Komzifti is once daily; Revuforj is twice daily. Both labels carry boxed warnings including differentiation syndrome and QTc prolongation. Johnson & Johnson's bleximenib is in development. Within AML more broadly, Revuforj sits alongside AbbVie and Genentech's venetoclax, Astellas's gilteritinib, Servier's ivosidenib and Daiichi Sankyo's quizartinib, which target different genotypes. In chronic GVHD, Niktimvo is used after Incyte's ruxolitinib, Sanofi's belumosudil and ibrutinib, so its own partner also owns the frontline standard it is being combined with in ongoing trials.
Why did SNDX stock drop?
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The shares have traded between $12.99 and $25.59 over the past year and were around $19.65 in August 2026, so the moves have been wide in both directions. Three identifiable pressures explain much of the weakness. Kura Oncology and Kyowa Kirin's ziftomenib was approved in November 2025 in the same NPM1-mutated indication Revuforj had just entered, ending a brief monopoly. First-quarter 2026 revenue then fell sequentially to $64.9M from $68.7M as the January payer and gross-to-net reset hit, which reads badly on a launch chart even when underlying demand is rising. And in June 2026 the company issued $250M of convertible notes with a conversion price near $24.76, adding about 10.1M potential shares against 89.4M outstanding. Set against that, second-quarter revenue of $72.8M was up 92% year over year.
Does SNDX pay a dividend?
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No. Syndax has never paid a dividend and does not currently generate net income, so there is no distributable profit. The company is spending roughly $400M a year on research and selling costs against ~$252M of trailing revenue and is funding the gap from a $575.1M cash and investments balance built partly from a $350M royalty monetisation and $250M of convertible notes. Both of those instruments carry claims that rank ahead of shareholders: the notes pay 2.25% semi-annual cash interest, and Royalty Pharma takes 13.8% of US Niktimvo net sales up to an $822.5M cap. Companies at this stage of a launch generally reinvest any surplus into trials rather than returning it, and Syndax's stated priority is reaching profitability rather than distributions.
How much cash does Syndax have, and will it need to raise more?
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Syndax held $575.1M in cash, cash equivalents and short and long-term investments at June 30, 2026, up from $394.1M at the end of 2025 after issuing $250M of 2.25% convertible senior notes due 2031 in June. Operating cash use in the first half of 2026 was $80.6M, roughly $161M annualised and falling as revenue grows against a flat cost base. On that arithmetic the balance covers several years, and management states it expects cash plus revenue and interest income to reach profitability without further financing. The caveats are real: the trials that matter most, the frontline AML Phase 3 programmes, are the most expensive part of the plan, and stockholders' equity was only $15.1M at June 30, 2026 against $688.6M of liabilities, so the cushion is in the cash balance rather than in the equity.
What are the next catalysts for SNDX in 2026?
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The fourth quarter of 2026 carries most of them. Topline data are expected from two Phase 2 trials of axatilimab: one in idiopathic pulmonary fibrosis, where enrollment completed in early 2026 and which would open a market well beyond transplant medicine, and one combining axatilimab with ruxolitinib in newly diagnosed chronic GVHD. Syndax also expects to publish safety and efficacy data in relapsed or refractory NUP98-rearranged acute leukemia in the fourth quarter, and has flagged frontline revumenib readouts from the BEAT AML, SAVE and intensive-chemotherapy trials at medical meetings in the second half of the year. Two new trials start around the same window: RAVEN in the second half of 2026 and the MenTain post-transplant maintenance study around year end. The pivotal EVOLVE-2 and REVEAL-ND Phase 3 trials are still enrolling.
Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with Syndax Pharmaceuticals, Inc.'s investor relations page or your broker before making investment decisions.