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Sep 30, 2024

Syndax Q3 2024 Earnings Report

Transitioned to a commercial-stage company with Niktimvo approval and secured royalty financing to fund operations through profitability.

Key Takeaways

Syndax reported its Q3 2024 financial results, highlighting the transition to a commercial-stage company with the approval of Niktimvo and a royalty financing agreement expected to fund the company through profitability.

Niktimvo approved by U.S. FDA for chronic GVHD treatment.

Revumenib NDA for R/R KMT2Ar acute leukemia under RTOR review with PDUFA date of December 26, 2024.

Topline data from AUGMENT-101 for mNPM1 AML expected in 4Q24.

$350 million royalty funding agreement for Niktimvo secured.

Total Revenue
$12.5M
0
EPS
-$0.98
Previous year: -$0.73
+34.2%
$71M
Previous year: $39.1M
+81.6%
$31.1M
Previous year: $17.3M
+80.1%
Gross Profit
$12.5M
Previous year: -$3K
-416700.0%
Cash and Equivalents
$400M
Previous year: $379M
+5.4%
Free Cash Flow
-$62.3M
Previous year: -$44.7M
+39.6%
Total Assets
$426M
Previous year: $399M
+6.7%

Syndax

Syndax

Forward Guidance

Syndax expects research and development expenses to be $245 to $250 million and total operating expenses to be $365 to $370 million for the full year of 2024. The company expects to reach profitability with current resources.

Positive Outlook

  • Cash, cash equivalents and marketable securities, together with the $350 million from the sale of a portion of the Niktimvo royalty and anticipated product revenue and interest income, enables the company to reach profitability.