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Kyverna Reports $41.9 Million Third-Quarter Loss as Miv-cel BLA Submission Completes

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Kyverna Therapeutics (KYTX) reported a third-quarter 2026 net loss of $41.9 million, or $0.68 per basic and diluted share, and said it completed submission of its biologics license application for miv-cel in stiff person syndrome.

The company ended September with $170.6 million in cash, cash equivalents and marketable securities. Kyverna said its available cash and amounts available under its amended Oxford Finance loan facility are expected to fund operations into 2028.

  • Third-quarter research and development expense was $27.0 million, while general and administrative expense was $15.9 million.
  • Kyverna requested priority review from the FDA for miv-cel, also known as mivocabtagene autoleucel or KYV-101, in stiff person syndrome.
  • Enrollment in the KYSA-6 Phase 3 trial of miv-cel for generalized myasthenia gravis remains on track for completion in mid-2027.
  • The company deprioritized its KYV-102 program to focus on late-stage neurologic indications for miv-cel.

$KYTX Hedge Fund Activity

We have seen 70 institutional investors add shares of $KYTX stock to their portfolio, and 52 decrease their positions in their most recent quarter.

Here are some of the largest recent moves:

To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard. You can access data on hedge funds moves and 13F filings through the Quiver Quantitative API 13F endpoint.

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