Dec 31, 2021

Checkpoint Therapeutics Q4 2021 Earnings Report

Reported financial results for the full-year ended December 31, 2021 and recent corporate highlights.

Key Takeaways

Checkpoint Therapeutics announced its full-year 2021 financial results, highlighting a transformational period with the foundation laid for value-enhancing catalysts in 2022, including a planned BLA submission for cosibelimab.

Checkpoint Therapeutics is focused on developing novel treatments for solid tumor cancers.

The company is evaluating cosibelimab, a potential best-in-class anti-PD-L1 antibody, in a Phase 1 clinical trial.

Checkpoint intends to submit a Biologics License Application for cosibelimab in metastatic cSCC later in 2022.

Olafertinib is being evaluated as a potential new treatment for patients with EGFR mutation-positive non-small cell lung cancer.

Total Revenue
$16K
Previous year: $27K
-40.7%
EPS
-$3.9
Previous year: -$1.7
+129.4%
Cash and Equivalents
$54.7M
Total Assets
$55.7M

Checkpoint Therapeutics

Checkpoint Therapeutics

Forward Guidance

Checkpoint Therapeutics anticipates multiple potentially value enhancing catalysts in 2022.

Positive Outlook

  • Planned Biologics License Application submission for cosibelimab.
  • Advancing pipeline of product candidates.
  • Expanding patient access globally to potentially life-saving novel oncology therapies.
  • Positive topline results from ongoing registrational trial of cosibelimab in metastatic cutaneous squamous cell carcinoma.
  • Focus on expeditiously advancing product candidates.

Challenges Ahead

  • Risk of delays in BLA submission.
  • Potential for safety issues or trends observed in clinical trials.
  • Risk that regulatory authorities may not accept application for approval.
  • Dependence on third-party suppliers.
  • Impact of evolving Russia/Ukraine conflict and COVID-19 pandemic.