Erasca reported financial results for Q2 2023, highlighting significant progress across all clinical programs, including promising data for ERAS-007 and ERAS-601. The company's cash runway extends into H2 2025, supported by a strong balance sheet with $365 million in cash, cash equivalents, and marketable securities.
Advanced clinical programs with Phase 1b combo data for ERAS-007 and ERAS-601.
ERAS-801 received FTD and ODD designations.
Naporafenib combination data was published.
Cash, cash equivalents, and marketable securities totaled $365 million, funding operations into H2 2025.
Erasca anticipates several key milestones, including dosing the first patient in the SEACRAFT-1 Phase 1b trial and initial Phase 1 monotherapy dose escalation data for ERAS-801 in recurrent GBM, both expected in the second half of 2023.