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Mar 31

RAPT Q1 2025 Earnings Report

RAPT Therapeutics reported financial results for the first quarter ended March 31, 2025.

Key Takeaways

RAPT Therapeutics reported a significant decrease in net loss for the first quarter of 2025 compared to the same period in 2024, primarily driven by a reduction in research and development expenses.

Net loss for Q1 2025 was $17.2 million, a substantial improvement from the $30.5 million loss in Q1 2024.

Research and development expenses decreased significantly to $12.0 million in Q1 2025 from $24.8 million in Q1 2024.

General and administrative expenses also saw a slight decrease, falling to $7.2 million in Q1 2025 from $7.7 million in Q1 2024.

As of March 31, 2025, the company held $179.3 million in cash, cash equivalents, and marketable securities.

Total Revenue
$0
0
EPS
-$0.08
Previous year: -$0.79
-89.9%
R&D Expenses
$12M
Previous year: $24.8M
-51.4%
G&A Expenses
$7.22M
Previous year: $7.74M
-6.6%
Cash and Equivalents
$60.3M
Previous year: $45.3M
+33.0%
Total Assets
$188M
Previous year: $156M
+20.4%

RAPT

RAPT

Forward Guidance

RAPT Therapeutics is focused on advancing its lead program, RPT904, with plans to initiate a Phase 2b trial in food allergy and expects clinical data from its partner Jemincare for RPT904 in chronic spontaneous urticaria.

Positive Outlook

  • Planned initiation of a Phase 2b trial for RPT904 in food allergy in the second half of 2025.
  • Expectation of clinical data from partner Jemincare for RPT904 in chronic spontaneous urticaria later in 2025.
  • Belief that RPT904 has the potential to be a best-in-class treatment for food allergy.
  • Excitement about RPT904's potential as a treatment for chronic spontaneous urticaria.
  • Making good progress towards planned clinical trial initiation.

Challenges Ahead

  • Potential for unexpected or unfavorable safety or efficacy data in clinical studies.
  • Preliminary data and trends may not be predictive of future results or regulatory approval.
  • Reliance on partners and other third parties.
  • Clinical trial site activation or enrollment rates may be lower than expected.
  • Unanticipated or greater than anticipated impacts or delays due to macroeconomic and geopolitical conditions.