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Sep 30, 2023

Tempest Q3 2023 Earnings Report

Reported financial results for the third quarter ended September 30, 2023 and provided a corporate update.

Key Takeaways

Tempest Therapeutics reported data demonstrating superiority of TPST-1120 across multiple study endpoints in first-line hepatocellular carcinoma. As of November 7, 2023, preliminary cash and cash equivalents were $32.8 million. Net loss for the quarter ended September 30, 2023 was $6.8 million and $0.48 per share.

TPST-1120 demonstrated superiority compared to standard of care across multiple study endpoints in randomized first-line HCC study

Confirmed objective response rate of 30% for the TPST-1120 triplet arm as compared to 13.3% for the atezolizumab + bevacizumab control arm

New capital strengthens balance sheet and extends cash runway into 2025

Plan to advance TPST-1120 into a registrational study in first-line liver cancer patients, likely in connection with a partnership.

Total Revenue
$0
0
EPS
-$0.48
Previous year: -$0.66
-27.3%
Gross Profit
-$510K
Cash and Equivalents
$11.1M
Previous year: $42.8M
-74.0%
Free Cash Flow
-$6.49M
Previous year: -$9.18M
-29.3%
Total Assets
$24M
Previous year: $63.2M
-62.0%

Tempest

Tempest

Forward Guidance

Tempest Therapeutics plans to advance TPST-1120 into a registrational study in first-line liver cancer patients, likely in connection with a partnership. Expect to report data from the combination arm at the two highest TPST-1495 doses in patients with advanced endometrial cancer in 2024. Plan to advance new proprietary small molecule series TREX1 inhibitors generated through insights resulting from human TREX1-inhibitor co-crystal structures with the goal to select a lead or development candidate by the end of 2023 or early 2024.

Positive Outlook

  • Advance TPST-1120 into a registrational study in first-line liver cancer patients
  • Report data from the combination arm at the two highest TPST-1495 doses in patients with advanced endometrial cancer in 2024
  • Advance new proprietary small molecule series TREX1 inhibitors
  • Goal to select a lead or development candidate by the end of 2023 or early 2024
  • New capital extends the Company’s cash runway into 2025

Challenges Ahead

  • Unexpected safety or efficacy data observed during preclinical or clinical trials
  • Clinical trial site activation or enrollment rates that are lower than expected
  • Changes in expected or existing competition
  • Changes in the regulatory environment
  • Unexpected litigation or other disputes