•
Sep 30, 2023

Tyra Biosciences Q3 2023 Earnings Report

Reported third quarter financial results and corporate progress.

Key Takeaways

Tyra Biosciences reported a net loss of $21.2 million for the third quarter of 2023 and highlighted the advancement of TYRA-300 in the SURF301 oncology study, positive preclinical data for achondroplasia, and the expected initiation of the TYRA-200 Phase 1 study by the end of 2023. The company's cash and cash equivalents totaled $215.7 million as of September 30, 2023.

Enrollment and dose escalation are ongoing in the SURF301 Phase 1/2 oncology study.

Additional preclinical data on TYRA-300 in achondroplasia were presented at ASBMR and ASHG meetings.

The first patient is expected to be dosed in the TYRA-200 Phase 1 study by the end of 2023.

Tyra Biosciences reported a strong cash position of $215.7 million as of Q3 2023.

Total Revenue
$0
EPS
-$0.49
Previous year: -$0.3
+63.3%
Gross Profit
-$82K
Cash and Equivalents
$216M
Previous year: $263M
-18.0%
Free Cash Flow
-$17.2M
Previous year: -$12.3M
+40.5%
Total Assets
$238M
Previous year: $276M
-13.6%

Tyra Biosciences

Tyra Biosciences

Forward Guidance

Tyra Biosciences anticipates several key milestones, including updating guidance on the timing and design of the planned Phase 2 study in achondroplasia and dosing the first patient with TYRA-200.

Positive Outlook

  • Continued advancement of TYRA-300 in the SURF301 oncology study.
  • Strengthening of preclinical data package in achondroplasia for TYRA-300.
  • Expected update on the timing and design of the planned Phase 2 study in achondroplasia.
  • Anticipated dosing of the first patient with TYRA-200 before the end of the year.
  • Advancement of the in-house precision medicine discovery engine, SNÃ…P, to develop therapies in targeted oncology and genetically defined conditions.

Challenges Ahead

  • Potential delays in the commencement, enrollment, and completion of preclinical studies and clinical trials.
  • The approach to discover and develop drugs based on the SNÃ…P platform is novel and unproven.
  • Unexpected adverse side effects or inadequate efficacy of product candidates may limit their development, regulatory approval, and/or commercialization.
  • Dependence on third parties in connection with manufacturing, research, and preclinical testing.
  • Unstable market and economic conditions and adverse developments with respect to financial institutions and associated liquidity risk may adversely affect the business and financial condition.