Syndax Pharmaceuticals

Syndax Pharmaceuticals (SNDX) Q4 2025 Earnings

Reported Feb 26, 2026 at 4:02 PM ET · SEC Source

Q4 25 EPS

$-0.78

MISS 34.88%

Est. $-0.58

Q4 25 Revenue

$68.7M

BEAT +6.15%

Est. $64.7M

vs S&P Since Q4 25

+2.1%

BEATING MARKET

SNDX +11.3% vs S&P +9.2%

Full Year 2025 Results

FY 25 EPS

$-3.29

FY 25 Revenue

$172.4M

Market Reaction

Did SNDX Beat Earnings? Q4 2025 Results

Syndax Pharmaceuticals capped a transformative year with a strong commercial quarter, reporting Q4 2025 revenue of $68.73 million against a net loss of $0.78 per share, as its twin FDA-approved therapies continued to gain meaningful clinical traction… Read more Syndax Pharmaceuticals capped a transformative year with a strong commercial quarter, reporting Q4 2025 revenue of $68.73 million against a net loss of $0.78 per share, as its twin FDA-approved therapies continued to gain meaningful clinical traction. The primary engine of that growth was Revuforj, which generated $44.20 million in Q4 net product revenue, a 38% sequential increase fueled by the October 2025 label expansion into NPM1-mutated AML and a 35% quarter-over-quarter rise in total prescriptions to roughly 1,150. Niktimvo, co-commercialized with Incyte for chronic GVHD, contributed an additional $19.39 million to Syndax's share of collaboration profit. Full-year 2025 revenue reached $172.35 million, up sharply from $23.68 million in 2024, underscoring just how rapidly the company has pivoted from development to commercial stage. Looking ahead, management guided combined R&D and SG&A expenses of approximately $400 million for 2026, while expressing confidence that growing product revenues and a stable cost base will carry the company to profitability without requiring additional capital raises.

Key Takeaways

  • Revuforj Q4 net revenue increased 38% quarter-over-quarter driven by October 2025 FDA approval expanding label to R/R NPM1m AML
  • Total Revuforj prescriptions grew approximately 35% quarter-over-quarter to approximately 1,150 in Q4
  • Niktimvo net revenue grew 22% quarter-over-quarter to $56.0 million in Q4
  • Growing adoption of Revuforj in R/R NPM1m AML with early indicators suggesting ≥30% of new patient starts were NPM1 in Q4
  • Approximately 90% of U.S. BMT centers have ordered Niktimvo
  • 60-70% of patients who started Niktimvo in Q1 2025 remained on therapy at month 10
  • Growing combination use of Revuforj with approximately 40% of use in combination
  • Approximately 70% of Revuforj use in second/third line treatment
24/7 Wall St

SNDX YoY Financials

Q4 2025 vs Q4 2024, source: SEC Filings

24/7 Wall St

SNDX Revenue by Segment

With YoY comparisons, source: SEC Filings

Q1 25 Q1 26

“We solidified our leadership position and proved the strength of Syndax's R&D and commercial capabilities in 2025, achieving our third FDA approval and successfully launching two first- and best-in-class medicines. We reached thousands of patients with Revuforj and Niktimvo and generated over $275 million in 2025 sales, rapidly advancing the company towards profitability.”

— Michael A. Metzger, Q4 2025 Earnings Press Release