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Dec 31, 2022

Viking Therapeutics Q4 2022 Earnings Report

Reported financial results for the fourth quarter and year ended December 31, 2022, and provided a corporate update.

Key Takeaways

Viking Therapeutics reported a net loss of $19.6 million, or $0.26 per share, for the three months ended December 31, 2022. The company ended the quarter with a strong cash position of approximately $155 million, providing an operating runway that extends beyond the key milestones for its clinical programs.

Enrollment completed in Phase 2b VOYAGE study of VK2809 for NASH and Fibrosis; data expected in 2Q 2023.

Phase 1 study of dual GLP-1/GIP agonist VK2735 continues; data expected in 1Q 2023.

Phase 1b study of VK0214 in X-ALD patients continues to enroll; data expected in 2H23.

Ended the fourth quarter with $155 million in cash, cash equivalents and short-term investments.

EPS
-$0.26
Previous year: -$0.16
+62.5%
R&D Expenses
$16.2M
Previous year: $9.85M
+64.3%
G&A Expenses
$4.11M
Previous year: $2.66M
+54.1%
Cash and Equivalents
$36.6M
Previous year: $26.4M
+38.9%
Total Assets
$169M
Previous year: $211M
-20.0%

Viking Therapeutics

Viking Therapeutics

Forward Guidance

Viking expects to report data from all three of its active clinical programs in 2023.

Positive Outlook

  • Initial data from Phase 2b VOYAGE trial of VK2809 for NASH and fibrosis expected in 2Q 2023.
  • Initial data from Phase 1 study evaluating dual-agonist compound VK2735 expected later this quarter.
  • Data from Phase 1b trial evaluating VK0214 in X-ALD patients expected later this year.
  • Strong cash position of approximately $155 million provides an operating runway that extends beyond the key milestones for clinical programs.
  • VK2809 demonstrated encouraging therapeutic potential in liver disorders, producing significant reductions in liver fat and plasma lipids in NAFLD patients with elevated lipids.

Challenges Ahead

  • Clinical trials are subject to risks and uncertainties.
  • Prior clinical and preclinical results may not be replicated.
  • Regulatory requirements may impact the development programs.
  • The company's expectations regarding its clinical and preclinical development programs and cash resources may not be accurate.
  • The success, cost and timing of Viking's product candidate development activities and clinical trials are subject to risks.