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Kyverna Therapeutics Presents Full One-Year Registrational Data Set Demonstrating Sustained Clinical Benefit of Miv-cel in Stiff Person Syndrome at MS Toronto

$KYTXPress releaseOct 21, 2026, 7:15 AM ETRead the release

Kyverna presented full one-year registrational data for miv-cel in stiff person syndrome at the ACTRIMS-ECTRIMS joint meeting, showing durable efficacy with T25FW improvement of 49% at one year and 92% of patients remaining free of chronic immunotherapies. Safety remained well-tolerated, with no high-grade CRS, ICANS, or IEC-HS cases in one-year follow-up; grade 3/4 neutropenia occurred in five patients and serious treatment-related AEs in three, all fully resolved.

Key figures

Drug Name
miv-cel (mivocabtagene autoleucel, KYV-101)
Phase Of Trial
Phase 2 (registrational, single-arm)
Walk aid free
67% (8/12)
Sps patients us
6000
Patients treated
26
Patients treated to date
>100
T25fw improvement week16
46%
T25fw improvement one year
49%
Grade34 neutropenia patients
5
Six min walk improvement 1yr
119 meters
Serious treatment related aes
3
Six min walk improvement 16wk
89 meters
Pct meaningful improvement week16
81% (21/26)
Pct free of chronic immunotherapies
92% (24/26)
Pct meaningful improvement one year
77% (20/26)

AI analysis

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    KYTX: Kyverna Therapeutics Presents Full One-Year Registrational Data Set Demonstrating Sustained Clinical Benefit of Miv-cel in Stiff Person Syndrome at MS Toronto — AI Analysis | Signal8