TD Cowen 45th Annual Healthcare Conference
Logotype for Artiva Biotherapeutics Inc

Artiva Biotherapeutics (ARTV) TD Cowen 45th Annual Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Artiva Biotherapeutics Inc

TD Cowen 45th Annual Healthcare Conference summary

17 Dec, 2025

Company overview and strategy

  • Focuses on allogeneic NK cell therapy for autoimmune diseases and cancer, leveraging technology from a Korean spinout.

  • Lead program AlloNK is a non-genetically engineered, off-the-shelf NK cell combined with monoclonal antibodies.

  • Manufacturing process enables high scalability and low cost, with drug product stability exceeding three years.

  • Sourcing from umbilical cord blood with high affinity CD16 and KIR-B haplotype enhances efficacy.

  • Projected cost of goods is under $1,000 per billion cells, supporting commercial scalability.

Clinical development and data

  • AlloNK is in Phase I trials for multiple autoimmune indications, with initial data expected in the first half of the year.

  • Prior data in aggressive NHL patients showed deep and durable B cell depletion, mirroring auto CAR T outcomes.

  • Majority of NHL patients were treated outpatient, with a median hospital stay of three nights for those admitted.

  • Ongoing trials include a company-sponsored lupus study and a basket IIT in community rheumatology, exploring multiple indications.

  • Trials use reduced doses of fludarabine and cyclophosphamide, aiming for improved safety and outpatient administration.

Mechanism of action and differentiation

  • AlloNK enhances ADCC of monoclonal antibodies, allowing flexibility to target various B cell compartments.

  • High affinity CD16 on NK cells is linked to better outcomes in both oncology and autoimmune settings.

  • NK cell therapy avoids the CRS risks seen with T cell therapies, supporting use in community settings.

  • Ability to decouple activity from tolerability positions AlloNK favorably versus T cell engagers and CAR Ts.

  • No tocilizumab was needed in oncology trials, highlighting a favorable safety profile.

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