SNDXMEDIUM SIGNALREGULATORY10-K

SNDX achieved a second FDA approval for Revuforj in acute myeloid leukemia with NPM1 mutations in October 2025, expanding the commercial opportunity for their lead oncology asset.

The additional FDA approval for Revuforj represents meaningful progress in building a diversified oncology franchise, providing multiple revenue streams from a single asset. However, the company continues to face substantial cash burn and declining equity position, requiring careful monitoring of funding runway as they scale commercial operations.

Comparing 2026-02-26 vs 2025-03-03View on EDGAR →
FINANCIAL ANALYSIS

SNDX showed mixed financial performance with operating losses narrowing modestly year-over-year while SG&A expenses grew substantially, likely reflecting increased commercial activities following drug approvals. The balance sheet weakened considerably with stockholders' equity declining significantly and cash reserves decreasing, though operating cash flow deteriorated as the company continues investing in commercialization efforts. Overall, the financial picture reflects a company in transition from development to commercial stage with typical associated cash consumption patterns.

FINANCIAL STATEMENT CHANGES
Interest Expense
P&L
-93.4%
$3.1M$208K

Interest expense declined — debt repayment or refinancing at lower rates improving earnings quality.

Stockholders Equity
Balance Sheet
-77.6%
$288.1M$64.6M

Equity declined sharply — large losses, buybacks, or write-downs reducing book value significantly.

SG&A Expense
P&L
+48.6%
$120.9M$179.7M

SG&A up 48.6% — significant increase in sales or administrative costs, monitor impact on operating leverage.

Total Assets
Balance Sheet
-26.9%
$724.8M$529.7M

Total assets contracted 26.9% — asset sales, write-downs, or balance sheet optimization underway.

Operating Income
P&L
+19.6%
-$339.7M-$273.1M

Operating income improving — cost discipline or growing revenue base absorbing fixed costs.

Operating Cash Flow
Cash Flow
-17.5%
-$274.9M-$323.0M

Operating cash flow softened — monitor whether temporary working capital timing or structural deterioration.

Current Liabilities
Balance Sheet
+16%
$103.5M$120.1M

Current liabilities rose 16% — increased short-term obligations, watch current ratio.

Cash & Equivalents
Balance Sheet
-12.4%
$154.1M$134.9M

Cash decreased 12.4% — monitor burn rate and upcoming capital needs.

Current Assets
Balance Sheet
-12.4%
$603.1M$528.1M

Current assets declined 12.4% — monitor working capital adequacy and short-term liquidity.

Net Income
P&L
+10.5%
-$318.8M-$285.4M

Net income grew 10.5% — bottom-line growth signals improving overall business health.

LANGUAGE CHANGES
NEW — 2026-02-26
PRIOR — 2025-03-03
ADDED
As of February 23, 2026, th ere were 88,200,596 shares of common stock outstanding.
B USINESS Our Company We are a commercial-stage biopharmaceutical company advancing innovative cancer therapies.
We currently have two commercially approved medicines, Revuforj (revumenib) and Niktimvo (axatilimab-csfr), and a robust slate of clinical development programs designed to unlock the full potential of our first two products.
In October 2025, Revuforj received a second approval from the FDA for the treatment of R/R acute myeloid leukemia, or AML, with a susceptible nucleophosmin 1 mutation, or NPM1m, in adult and pediatric patients one year and older who have no satisfactory alternative treatment options.
Additionally, we are exploring the potential for menin inhibition in the treatment of myelofibrosis, or MF.
+7 more — sign up free →
REMOVED
As of February 24, 2025, there were 86,024,394 shares of common stock outstanding.
B USINESS Our Company We are a commercial-stage biopharmaceutical company developing an innovative pipeline of cancer therapies.
We currently have two commercially approved medicines and a robust slate of clinical development programs designed to unlock the full potential of our first two medicines.
In the second quarter of 2025, we expect to submit a supplemental New Drug Application, or sNDA, for revumenib as a treatment for R/R acute myeloid leukemia, or AML, with a nucleophosmin 1 mutation, or mNPM1, based on the positive pivotal data from our AUGMENT-101 trial.
Additionally, we are exploring the use of revumenib as a treatment in solid tumors, specifically its activity in metastatic colorectal cancer.
+7 more — sign up free →
ANALYZE ANY FILING FREE

See what changed in your portfolio's filings

500+ US-listed companies analyzed. Language delta, financial analysis, instant signal scoring.

Try Tracenotes free →