Corbus Pharmaceuticals reported a net loss of $9.5 million for Q4 2024, an increase from $8.0 million in Q4 2023. The company ended the year with $149.1 million in cash and investments, projecting a cash runway through Q3 2027. Significant progress was noted in its CRB-701 oncology program, which received Fast Track Designation, and its CRB-913 obesity program, with first-in-human dosing expected in March 2025.
CRB-701, a Nectin-4 targeting ADC, showed encouraging safety and efficacy results in its Phase 1 Western study, with clinical responses in urothelial and cervical cancer, and first-time responses in HNSCC.
The FDA granted Fast Track Designation to CRB-701 for the treatment of relapsed or refractory metastatic cervical cancer.
The CRB-913 obesity program is on track for first-in-human dosing in March 2025, with a Phase 1 dose-range finding study expected to commence in Q4 2025.
Corbus reported $149.1 million in cash, cash equivalents, and investments as of December 31, 2024, with a projected cash runway through Q3 2027.
Corbus Pharmaceuticals anticipates significant clinical data generation from its oncology and obesity programs in the second half of 2025, with key milestones including dose optimization for CRB-701 and the initiation of a Phase 1 dose-range finding study for CRB-913.