BSI 082
Alternative Names: BSI-082Latest Information Update: 04 Aug 2025
At a glance
- Originator Biosion
- Class Antineoplastics; Immunotherapies; Monoclonal antibodies
- Mechanism of Action Phagocyte stimulants; SIRPA protein inhibitors
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Preclinical Solid tumours
Most Recent Events
- 25 Jul 2025 Biosion in collaboration with The University of Texas Health Science Center plans a phase I trial for Solid tumours (Combination therapy, Monotherapy, Late-stage disease, Metastatic disease, Second-line therapy or greater) (IV, Infusion), in August 2025 (NCT07086768)
- 24 Jan 2024 Biosion receives IND approval from the U.S. Food and Drug Administration (US FDA) for BSI 082 for solid tumours
- 12 Sep 2022 Biosion plans to file an IND application for Solid tumours in second half of 2023 (Biosion pipeline, September 2022)