Vir Biotechnology reported a net loss of $(104.6) million for Q4 2024, an improvement from $(116.0) million in Q4 2023. Total revenues for the quarter were $12.4 million, down from $16.8 million in the prior year. The company ended the year with $1.10 billion in cash, cash equivalents, and investments, providing a cash runway into mid-2027.
Phase 3 ECLIPSE registrational clinical program in chronic hepatitis delta is on track to begin in the first half of 2025.
Tobevibart and elebsiran in chronic hepatitis delta received U.S. FDA Breakthrough and Fast Track designations, and EMA PRIME and Orphan Drug designations.
Dual-masked T-cell engagers VIR-5818 and VIR-5500 showed compelling early clinical response signals and promising safety profiles in solid tumors.
The company plans to initiate a Phase 1 study of VIR-5525, its dual-masked EGFR-targeting T-cell engager, in the first half of 2025.
Based on current operating plans, Vir Biotechnology expects its cash, cash equivalents, and investments to fund its operations into mid-2027.
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