Syndax Pharmaceuticals

Syndax Pharmaceuticals (SNDX) Q1 2026 Earnings

Reported Apr 30, 2026 at 4:02 PM ET · SEC Source

Q1 26 EPS

$-0.48

BEAT +18.75%

Est. $-0.59

Q1 26 Revenue

$64.9M

MISS 7.11%

Est. $69.8M

vs S&P Since Q1 26

-9.2%

TRAILING MARKET

SNDX -1.9% vs S&P +7.3%

Market Reaction

Did SNDX Beat Earnings? Q1 2026 Results

Syndax Pharmaceuticals delivered a mixed but broadly encouraging first quarter for fiscal 2026, posting a narrower-than-expected loss while revenue, though shy of forecasts, reflected explosive year-over-year growth across both of its commercial prod… Read more Syndax Pharmaceuticals delivered a mixed but broadly encouraging first quarter for fiscal 2026, posting a narrower-than-expected loss while revenue, though shy of forecasts, reflected explosive year-over-year growth across both of its commercial products. The company reported a net loss of $0.48 per share, beating the consensus estimate of $0.59 by 18.75%, even as revenue of $64.86 million fell about 7.11% short of the $69.83 million analysts had anticipated. The top-line figure nonetheless represented a 223.6% increase from the year-ago period, fueled primarily by Revuforj net revenue of $48.92 million and Niktimvo collaboration revenue of $15.94 million, with total prescriptions for Revuforj up roughly 160% year-over-year as adoption in NPM1-mutated AML continued to broaden. The net loss narrowed sharply to $42.67 million from $84.85 million a year earlier, reflecting the revenue ramp and lower operating expenses. Looking ahead, management expects its roughly $400 million combined R&D and SG&A expense base to hold steady and anticipates that revenue growth, including anticipated clinical catalysts in late 2026, will carry the company to profitability.

Key Takeaways

  • Increasing uptake of Revuforj in R/R NPM1-mutated AML with over 40% of Q1 new patients being NPM1m
  • Total Revuforj prescriptions increased ~160% year-over-year and ~13% sequentially
  • Nearly 50% of KMT2A patients proceeding to HSCT, up from prior 33% estimate, with ~45% resuming therapy post-transplant
  • 97% of all covered lives have formulary coverage for both Revuforj indications
  • Niktimvo captured ~32% share of 3L+ chronic GVHD market within first year of launch
  • ~60-70% of patients who started Niktimvo in Q1 2025 remained on treatment in Q1 2026
  • ~300 new patient starts for Niktimvo in Q1 2026 with ~5,000 infusions administered
  • R&D and SG&A expenses decreased year-over-year due to lower launch costs and milestone expenses
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SNDX YoY Financials

Q1 2026 vs Q1 2025, source: SEC Filings

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SNDX Revenue by Segment

With YoY comparisons, source: SEC Filings

Q1 25 Q2 26

“We delivered over $100 million in combined Revuforj and Niktimvo net sales in the first quarter, highlighting strong demand for our medicines and advancing the company towards profitability. Revuforj net revenue totaled $49 million, underscoring our leadership in menin inhibition and strong adoption in both R/R NPM1m AML and KMT2Ar acute leukemia. Notably, recent analysis indicates that Revuforj is enabling nearly half of KMT2A patients to receive a stem cell transplant, providing the best chance for durable remission and positioning the franchise for long-term growth as an increasing number of patients return to therapy post-transplant.”

— Michael A. Metzger, Q1 2026 Earnings Press Release