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Dec 31, 2022

Repare Therapeutics Q4 2022 Earnings Report

Reported financial results for the fourth quarter and full year ended December 31, 2022.

Key Takeaways

Repare Therapeutics reported fourth-quarter financial results, featuring revenue from collaboration agreements of $18.2 million and a net loss of $31.7 million. The company highlighted progress in its pipeline, including the collaboration with Roche on camonsertib and the Fast Track designation for RP-6306.

Advanced camonsertib in partnership with Roche, with initial data expected in H1 2023.

Reported initial Phase 1 clinical data for RP-6306 as a monotherapy for advanced solid tumors in the first half of 2023, and combination therapy data in Q4 2023.

FDA granted Fast Track designation to RP-6306 in combination with gemcitabine for platinum-resistant ovarian cancer.

Initiated IND-enabling studies for a small molecule against an undisclosed target, with potential clinical entry in late 2023 or early 2024.

Total Revenue
$18.2M
Previous year: $6.88M
+164.6%
EPS
-$0.75
Previous year: -$0.7
+7.1%
Cash and Equivalents
$160M
Previous year: $334M
-52.3%
Free Cash Flow
-$27.9M
Previous year: -$20.9M
+33.6%
Total Assets
$364M
Previous year: $369M
-1.3%

Repare Therapeutics

Repare Therapeutics

Forward Guidance

Repare Therapeutics anticipates a productive 2023, with early clinical readouts for camonsertib and RP-6306 expected in the first half of the year and plans to expand its pipeline.

Positive Outlook

  • Initial data from Phase 1/2 trials of camonsertib in combination with PARP inhibitors expected in H1 2023.
  • Initial data from the Phase 1/2 TRESR trial evaluating camonsertib in combination with gemcitabine expected in summer or fall 2023.
  • Initial Phase 1 clinical data for RP-6306 as a monotherapy expected in H1 2023.
  • Initial Phase 1 clinical data for RP-6306 as a combination therapy expected in Q4 2023.
  • Initiation of IND-enabling studies for a small molecule against an undisclosed target in H1 2023.

Challenges Ahead

  • Prioritization of other Polθ inhibiting compounds may delay clinical entry for a Polθ inhibitor to 2024.
  • Macroeconomic conditions, including the COVID-19 pandemic and rising inflation, could impact the business.
  • Unexpected safety or efficacy data observed during preclinical studies or clinical trials.
  • Clinical trial site activation or enrollment rates that are lower than expected.
  • Changes in the regulatory environment and the uncertainties of the regulatory approval process.