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Dec 31, 2024

Belite Bio Q4 2024 Earnings Report

Belite Bio reported increased research and development expenses and a higher net loss in Q4 2024.

Key Takeaways

Belite Bio's Q4 2024 net loss widened to $10.1 million due to increased R&D expenses related to its clinical trials. The company did not generate revenue, as it remains in the development stage. Cash and investments totaled $145.2 million, providing runway for ongoing trials. The pivotal Phase 3 DRAGON trial continues as planned, with completion expected in Q4 2025.

Belite Bio reported a Q4 2024 net loss of $10.1 million, compared to $7.0 million in Q4 2023.

R&D expenses increased to $7.3 million, up from $4.9 million in Q4 2023, due to trial progress.

The company raised $15 million in a direct offering to support clinical development.

Cash and investments totaled $145.2 million, ensuring funding for ongoing trials.

Total Revenue
$0
0
EPS
-$0.32
Previous year: -$0.25
+28.0%
R&D Expenses
$7.25M
Previous year: $4.86M
+49.2%
General & Admin Expenses
$4.2M
Previous year: $2.09M
+100.8%
Cash and Equivalents
$31.7M
Previous year: $88.2M
-64.1%
Total Assets
$152M
Previous year: $94.6M
+60.7%

Belite Bio

Belite Bio

Forward Guidance

Belite Bio remains focused on advancing its clinical pipeline, with completion of key trials expected in late 2025.

Positive Outlook

  • Phase 3 DRAGON trial remains on track with no modifications recommended.
  • Enrollment in the PHOENIX trial for geographic atrophy increased to 406 subjects.
  • Sufficient cash and investments to fund operations through key milestones.
  • Potential additional $15 million in proceeds from warrant exercises.
  • Continued regulatory engagement for Tinlarebant’s approval pathway.

Challenges Ahead

  • No revenue generation as the company remains in the development stage.
  • R&D expenses continue to rise with trial progress, increasing cash burn.
  • Dependence on external funding to support long-term operations.
  • Regulatory uncertainties in securing approvals across global markets.
  • Potential delays in clinical trial completion due to enrollment challenges.