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Jun 30, 2022

Tyra Biosciences Q2 2022 Earnings Report

Reported financial results for the second quarter of 2022 and highlighted recent corporate progress.

Key Takeaways

Tyra Biosciences reported a net loss of $15.1 million for the second quarter of 2022. The FDA cleared the company to proceed with its SURF301 study of TYRA-300, and the IND for TYRA-200 is on track to be filed in the second half of 2022. The company had cash and cash equivalents of $275.1 million as of Q2 2022.

Received IND clearance from FDA to proceed with SURF301 Study of TYRA-300.

Pipeline on track; IND for TYRA-200 to be filed in 2H 2022.

The U.S. Food and Drug Administration (FDA) cleared TYRA to proceed with its Phase 1/2 SURF301 clinical study of TYRA-300.

Strengthened Leadership Team with Key Hires.

EPS
-$0.36
Previous year: -$4.54
-92.1%
Cash and Equivalents
$275M
Previous year: $135M
+103.5%
Free Cash Flow
-$17.4M
Previous year: -$4.7M
+270.5%
Total Assets
$287M

Tyra Biosciences

Tyra Biosciences

Forward Guidance

Statements contained in this press release regarding matters that are not historical facts are forward-looking statements.

Positive Outlook

  • Potential to develop purpose-built therapies that improve clinical outcomes
  • Expected IND submission timing for TYRA-200.
  • Ability to maintain undisrupted business operations due to the COVID-19 pandemic
  • Ability to obtain and maintain intellectual property protection for our product candidates and proprietary technologies
  • Developing a pipeline of selective inhibitors of Fibroblast Growth Factor Receptors (FGFR)

Challenges Ahead

  • Early in development efforts, have not tested any of product candidates in clinical trials
  • Approach to discover and develop drugs based on SNÃ…P platform is novel and unproven
  • Potential delays in the commencement, enrollment, and completion of preclinical studies and clinical trials
  • Dependence on third parties in connection with manufacturing, research and preclinical testing
  • Unexpected adverse side effects or inadequate efficacy of product candidates that may limit their development, regulatory approval, and/or commercialization