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Jun 30, 2024

Erasca Q2 2024 Earnings Report

Erasca's second quarter of 2024 was marked by the in-licensing of RAS-targeting molecules and the initiation of the SEACRAFT-2 Phase 3 trial.

Key Takeaways

Erasca reported a net loss of $63.2 million for the second quarter of 2024. The company initiated the SEACRAFT-2 Phase 3 trial and in-licensed two preclinical RAS programs. They also extended their cash runway into the first half of 2027 with $460.2 million in cash, cash equivalents, and marketable securities as of June 30, 2024.

Initiated SEACRAFT-2 registrational trial in patients with NRASm melanoma.

In-licensed potential best-in-class pan-RAS molecular glue ERAS-0015 and potential first-in-class pan-KRAS inhibitor ERAS-4001.

Extended cash runway into H1 2027 with $460.2 million in cash, cash equivalents, and marketable securities as of June 30, 2024.

Initial Phase 1b combination signal-seeking efficacy data from SEACRAFT-1 expected in Q4 2024.

Total Revenue
$0
EPS
-$0.29
Previous year: -$0.21
+38.1%
Gross Profit
-$1.1M
Cash and Equivalents
$460M
Previous year: $365M
+26.0%
Free Cash Flow
-$29.2M
Previous year: -$26.2M
+11.4%
Total Assets
$526M
Previous year: $441M
+19.3%

Erasca

Erasca

Forward Guidance

Erasca anticipates several key milestones, including data readouts from SEACRAFT-1 and SEACRAFT-2 trials, and IND filings for AURORAS-1 and BOREALIS-1 trials.

Positive Outlook

  • Initial Phase 1b combination signal-seeking efficacy data in relevant tumor types expected to be reported in Q4 2024 from SEACRAFT-1.
  • Phase 3 Stage 1 randomized dose optimization data expected to be reported in 2025 from SEACRAFT-2.
  • IND filing expected in H1 2025 for AURORAS-1.
  • Initial Phase 1 monotherapy data in relevant tumor types expected to be reported in 2026 from AURORAS-1.
  • IND filing expected in Q1 2025 for BOREALIS-1.

Challenges Ahead

  • Potential delays in the commencement, enrollment, data readout of clinical trials.
  • Unexpected adverse side effects or inadequate efficacy of product candidates.
  • Unfavorable results from preclinical studies or clinical trials.
  • Inability to realize any benefits from current licenses, acquisitions, and collaborations.
  • Dependence on third parties in connection with manufacturing, research, and preclinical and clinical testing.