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Erasca (ERAS) investor relations material
Erasca 44th Annual J.P. Morgan Healthcare Conference summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Strategic focus and pipeline overview
Focused on RAS-MAPK pathway with two lead programs: ERAS-15 (pan-RAS) and ERAS-4001 (pan-KRAS), both targeting solid tumors.
ERAS-15 and ERAS-4001 exhibit strong preclinical activity, high oral bioavailability, and robust intellectual property protection through 2043.
ERAS-15 demonstrates high potency, requiring one-tenth the dose of a key competitor to achieve similar tumor regression in preclinical models.
ERAS-4001 shows potent inhibition across KRAS mutations and wild-type, with promising PK and a potential wide therapeutic window.
Both programs are supported by a strong scientific advisory board and significant cash runway into the second half of 2028.
Clinical development and early data
AURORAS-1 (ERAS-15) first-in-human trial is enrolling briskly, targeting patients with advanced RAS mutations and no prior RAS inhibitor treatment.
Early clinical data for ERAS-15 show confirmed and unconfirmed partial responses at low doses, with all responding patients remaining on treatment at data cutoff.
Safety and tolerability profile for ERAS-15 is favorable, with no dose-limiting toxicities and predominantly low-grade adverse events.
Top-line safety, PK, and efficacy data for dozens of patients are expected in the first half of the year, with expansion and combination cohorts planned for the second half.
ERAS-4001 is enrolling in the BOREALIS-1 trial, with phase 1 monotherapy data expected in the second half of the year.
Differentiation, competitive landscape, and future plans
ERAS-15’s high binding affinity to CyPA leads to superior tumor distribution, longer residence time, and enhanced potency compared to competitors.
Early clinical responses at much lower doses than competitors suggest potential best-in-class status for ERAS-15.
No numerical ORR threshold is set; focus is on the totality of safety, tolerability, PK, and efficacy data.
Commercial strategy considers both best-in-class and second-in-class scenarios, with significant unmet need supporting multiple entrants.
Combination strategies for both molecules will be data-driven, with potential for use alongside standard of care and investigational agents.
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