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Jun 30, 2023

Tempest Q2 2023 Earnings Report

Reported financial results for the second quarter of 2023 and provided a corporate update.

Key Takeaways

Tempest Therapeutics reported a net loss of $7.6 million, or $0.54 per share, for the quarter ended June 30, 2023. The company ended the quarter with $17.6 million in cash and cash equivalents. They also presented data from their TPST-1495 and TPST-1120 programs.

Presented data from TPST-1495 at ASCO and in Cancer Research Communications.

Announced early triplet data from the TPST-1120 program demonstrating improvement in first-line HCC patients.

TPST-1120 triplet arm showed unconfirmed responses of 30% vs 17.2% for the control arm.

TPST-1495 continued enrollment of an endometrial cancer-specific arm investigating the two highest doses of TPST-1495 in combination with pembrolizumab.

Total Revenue
$0
0
EPS
-$0.54
Previous year: -$0.79
-31.6%
Cash and Equivalents
$17.6M
Previous year: $51.6M
-65.9%
Free Cash Flow
-$6.51M
Previous year: -$8.51M
-23.5%
Total Assets
$30.7M
Previous year: $71.4M
-56.9%

Tempest

Tempest

Forward Guidance

The company anticipates several milestones including discussing an updated data set from the TPST-1120 trial in the second half of 2023 and reporting data from the TPST-1495 combination arm in 2024.

Positive Outlook

  • Expect to discuss an updated and comprehensive data set from the formal review of the ongoing, global, randomized Phase 1b/2 study in first-line liver cancer patients in the second half of 2023 regarding TPST-1120.
  • Plan to report data from the combination arm at the two highest TPST-1495 doses in patients with advanced endometrial cancer in 2024.
  • Expect to advance new proprietary small molecule series TREX1 inhibitors generated through insights resulting from human TREX1-inhibitor co-crystal structures.
  • TPST-1120 combined with atezolizumab and bevacizumab showed positive early results in HCC study.
  • TPST-1495 showed increased potency against prostaglandin-driven tumor models.

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