Vir Scores In Oncology Pivot With Strong Early T-Cell Engager Results

Five months after taking over the dual-masked T-cell engagers from Sanofi amid a restructuring, the company posted promising initial Phase I data from its PSMA- and HER2-targeting IO candidates.

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Vir Biotechnology’s move from focusing solely on antiviral drugs to incorporating oncology into its pipeline has shown early signs of potentially paying off as the company announced safety and efficacy data for two T-cell engager (TCE) antibodies, VIR-5818 and VIR-5500, which it licensed from Sanofi in August.

The San Francisco-based biotech announced 8 January what it called encouraging safety and efficacy data from dose-escalation trials of VIR-5818, its HER2xCD3-directed TCE for solid tumors, and VIR-5500, its PSMAxCD3-directed TCE for

Key Takeaways
  • Vir’s VIR-5818 and VIR-5500 showed encouraging early signs of efficacy and tolerability in patients with breast, colorectal and prostate cancers.
  • The data provide validation for the dual-masking technology platform, which Vir acquired from Sanofi in August 2024

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