Erasca reported positive preliminary monotherapy data for ERAS-007 and ERAS-601, signed CTCSAs with Eli Lilly and Pfizer, and a strategic R&D collaboration with MD Anderson. The company's cash, cash equivalents, and marketable securities totaled $365 million.
Reported promising preliminary Phase 1/1b data for ERAS-007 and ERAS-601 in advanced solid tumors.
Signed CTCSAs with Eli Lilly to supply cetuximab in combination with ERAS-601 and with Pfizer to supply palbociclib in combination with ERAS-007.
Entered a strategic R&D collaboration with MD Anderson.
Expects to file an IND for CNS-penetrant KRAS G12C inhibitor ERAS-3490 before year-end.
Erasca anticipates filing an IND for ERAS-3490 in KRAS G12C mutant NSCLC before year-end. In the first half of 2023, they expect to initiate a dose escalation trial for ERAS-007 in combination with ERAS-601 and report combination data for ERAS-007 in gastrointestinal malignancies and ERAS-601 in triple wildtype CRC.