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Dec 31, 2024

Bioxcel Therapeutics Q4 2024 Earnings Report

BioXcel Therapeutics reported a reduced net loss in Q4 2024, driven by significant decreases in R&D and SG&A expenses, while continuing to generate modest revenue from IGALMI.

Key Takeaways

In Q4 2024, BioXcel Therapeutics posted $366,000 in revenue from IGALMI, with a net loss of $10.86 million or -$3.57 per share. Both R&D and SG&A expenses were significantly reduced compared to the prior year, contributing to a narrower operating loss. The company ended the quarter with $29.85 million in cash and continues to focus on advancing the SERENITY and TRANQUILITY programs.

Revenue from IGALMI was $366,000 in Q4 2024, slightly down from the prior year.

Net loss narrowed to $10.86 million from $22.26 million in Q4 2023.

R&D expenses dropped to $5.9 million from $9.9 million year-over-year.

Cash and cash equivalents totaled $29.85 million at the end of Q4 2024.

Total Revenue
$366K
Previous year: $376K
-2.7%
EPS
-$3.57
Previous year: -$0.76
+369.7%
R&D Expenses
$5.9M
Previous year: $9.93M
-40.6%
G&A Expenses
$4.09M
Previous year: $9.6M
-57.4%
Cash and Equivalents
$29.9M
Previous year: $65.2M
-54.2%
Total Assets
$38.3M
Previous year: $73.7M
-48.0%

Bioxcel Therapeutics

Bioxcel Therapeutics

Bioxcel Therapeutics Revenue by Segment

Forward Guidance

BioXcel plans to advance its SERENITY and TRANQUILITY Phase 3 trials, aiming for topline data in 2025 and targeting potential label expansions for IGALMI.

Positive Outlook

  • SERENITY At-Home trial enrollment over 60% complete.
  • TRANQUILITY In-Care Phase 3 trial protocol supported by FDA feedback.
  • Cash position strengthened to support development programs.
  • Topline data for SERENITY expected in second half of 2025.
  • Focus on BXCL501 as a core neuroscience asset with expansion potential.

Challenges Ahead

  • Minimal revenue generated from IGALMI sales.
  • Cash and equivalents declined from the prior year.
  • Ongoing net losses due to high development and operational costs.
  • Commercial efforts remain limited with minimal marketing support.
  • Regulatory risks remain for investigational uses of BXCL501.