Kyverna reports one-year data for miv-cel in stiff person syndrome and myasthenia gravis
The company said 12-month results from its SPS trial and longer-term follow-up in gMG support a BLA submission on track for completion in Q4 2026.
SEC filing
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The company said 12-month results from its SPS trial and longer-term follow-up in gMG support a BLA submission on track for completion in Q4 2026.
SEC filing
Kyverna added a third RMAT designation for its CAR T therapy while keeping its stiff person syndrome and myasthenia gravis timelines on track.
SEC filing
The new agreement replaces a prior development pact and covers manufacturing for Kyverna's CAR T-cell therapy as it nears a possible U.S. approval in stiff person syndrome.
SEC filing