Clinical DevelopmentArtiva announced refractory rheumatoid arthritis will be prioritized as the lead autoimmune indication for AlloNK clinical development, leveraging its clean safety profile and scalability.
Regulatory MilestoneAlloNK + anti-CD20 mAb, rituximab, has been granted FDA Fast Track Designation for the treatment of refractory rheumatoid arthritis, marking it as the first deep B cell depleter to receive this designation.
Safety ProfileArtiva's AlloNK therapy reported no cases of ICANS or CRS and no Grade 3+ AlloNK-related adverse events, reinforcing its clean safety profile.