Skip to main content

kyv-101

Generic: Autologous Anti-CD19 CAR-CD8alpha-CD28-CD3zeta T Cells KYV 101·Code: KYV-101

kyv-101: developed by 1 company · 5 clinical trials tracked.

kyv-101 evidence translation

What we can confirm

What it means

Source-backed records connect kyv-101 to KYTX; that link alone does not prove the drug works.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

How could kyv-101 → KYTX affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 0 study sponsors

Study sponsors

No additional listed-company sponsor is linked.

Development Pipeline (1)
CompanyPhase
Kyverna Therapeutics, Inc. (KYTX)
Refractory Lupus Nephritis; Myasthenia Gravis; Systemic Scle…
Phase 1/Phase 2
Clinical Trials (5)

A Long-Term Follow-Up Study for Participants Previously Treated With KYV-101

Recruiting

Primary endpoint: Number of participants with treatment-related adverse events (AEs) as assessed by CTCAE v6.0 through Year 15 of long-term follow-up (LTFU).

Observational70 targetStarted 2025-11Completion 2041-011 site · United StatesKyverna Therapeutics

Comparison of B-cell Depletion by Rituximab and Anti-CD 19 CAR-T Therapy in Patients With Rheumatoid Arthritis. Two-stage Interventional, Prospective, Randomized, Controlled, Open Label, Parallel-group Phase I/II Trial in Patients With Active, ACPA-positive and Treatment Refractory Rheumatoid Arthritis

NCT06475495·Phase 1/Phase 2
Active, not recruiting

Primary endpoint: Safety Phase I (1) Safety

InterventionalRandomizedopen13 targetStarted 2024-12Completion 2027-061 site · GermanyCharite University, Berlin, Germany

KYSA-6: A Phase 2/3, Open-Label, Randomized, Controlled, Multicenter Study of KYV-101, an Autologous Fully Human Anti-CD19 Chimeric Antigen Receptor T-cell (CD19 CAR T) Therapy, Versus Ongoing Standard-Of-Care Immunosuppressive Therapy in Patients With Generalized Myasthenia Gravis

NCT06193889·Phase 2/Phase 3·KYTX
Recruiting

Primary endpoint: Incidence and severity of adverse events (AEs) and laboratory abnormalities (Phase 2)

InterventionalRandomizedopen66 targetStarted 2024-08Completion 2028-0922 sites · Australia, Brazil, Germany, Saudi Arabia…Kyverna Therapeutics

KYSA-5: A Phase 1/2, Open-Label, Multicentre Study of KYV 101, an Autologous Fully Human Anti-CD19 Chimeric Antigen Receptor T Cell (CD19 CAR T) Therapy, in Subjects With Systemic Sclerosis

NCT06400303·Phase 1/Phase 2·KYTX
Active, not recruiting

Primary endpoint: Incidence of adverse events and laboratory abnormalities (Phase 1)

Interventionalopen3 targetStarted 2024-08Completion 2027-032 sites · United StatesKyverna Therapeutics

CARTIMMUNE: A Single-Center Study of Patients With Autoimmune Diseases Receiving an Autologous Fully-Human Anti-CD19 Chimeric Antigen Receptor T-Cell (KYV 101)

NCT06152172·Phase 1
Active, not recruiting

Primary endpoint: Incidence and severity of AEs in IIM.

Interventionalopen24 targetStarted 2024-08Completion 2027-021 site · United StatesDavid Porter

Frequently asked questions

Who is developing kyv-101?

kyv-101 is being developed by Kyverna Therapeutics, Inc..

How many clinical trials involve kyv-101?

BioSniper tracks 5 clinical trials involving kyv-101.