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Mar 31, 2022

Corvus Pharmaceuticals Q1 2022 Earnings Report

Corvus Pharmaceuticals reported financial results for the first quarter of 2022 and provided a business update.

Key Takeaways

Corvus Pharmaceuticals reported a net loss of $8.3 million for the first quarter of 2022, compared to a net loss of $11.6 million for the same period in 2021. As of March 31, 2022, the company had cash, cash equivalents, and marketable securities totaling $62.9 million.

Advancing three clinical product candidates focused on tumor-immune system interaction.

Product candidates have demonstrated enhanced immune responses in various cancers.

Mid-to-late stage clinical trials for mupadolimab and ciforadenant are on track for initiation later this year.

ITK inhibitor shows encouraging potential in T cell differentiation for cancer and autoimmune diseases.

EPS
-$0.18
Previous year: -$0.34
-47.1%
Cash and Equivalents
$62.9M
Previous year: $68M
-7.5%
Total Assets
$101M
Previous year: $109M
-7.3%

Corvus Pharmaceuticals

Corvus Pharmaceuticals

Forward Guidance

Corvus is advancing three clinical programs in 2022, including plans for a Phase 2 study for mupadolimab in front-line non-small cell lung cancer (NSCLC), a Phase 1b/2 study for ciforadenant in front-line renal cell cancer (RCC), and the ongoing Phase 1/1b study for CPI-818 in T-cell lymphoma.

Positive Outlook

  • Advancing mupadolimab into a Phase 2 study for front-line NSCLC.
  • Progressing ciforadenant into a Phase 1b/2 study for front-line RCC.
  • Continuing the Phase 1/1b study for CPI-818 in T-cell lymphoma.
  • Plans to provide an update on these clinical programs at an R&D Symposium.
  • Demonstrated encouraging potential of ITK inhibitor on T cell differentiation

Challenges Ahead

  • The Company’s ability to demonstrate sufficient evidence of efficacy and safety in its clinical trials of mupadolimab, CPI-818 and ciforadenant
  • The accuracy of the Company’s estimates relating to its ability to initiate and/or complete preclinical studies and clinical trials
  • The results of preclinical studies may not be predictive of future results
  • The unpredictability of the regulatory process
  • The Company’s ability to raise additional capital