Ownership
Private
Employees
~100
Therapeutic Areas
Stage
Phase 1
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Modalities
SparX Biopharmaceutical General Information
First patient dosed with SPX-303 (anti-LILRB2/PD-L1 bispecific antibody) in April 2024. FDA approved IND application for SPX-303 in October 2023.
Contact Information
Primary Industry
Biotech
Corporate Office
Mount Prospect, Illinois
United States
United States
Drug Pipeline
SPX-303
Phase 1Key Partnerships
Arovella Therapeutics (for CLDN18.2-CAR-iNK development)
SparX Biopharmaceutical Funding
No funding data available
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Gosset