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Sep 30, 2023

RAPT Q3 2023 Earnings Report

RAPT Therapeutics reported financial results for Q3 2023, with a strong cash position maintained.

Key Takeaways

RAPT Therapeutics reported a net loss of $31.4 million for the third quarter of 2023. Research and development expenses were $27.0 million, and general and administrative expenses were $6.9 million. The company's cash, cash equivalents, and marketable securities totaled $184.8 million as of September 30, 2023, expected to support operations through mid-2025.

Progress continued with zelnecirnon in inflammatory diseases and tivumecirnon in oncology.

Top-line data from the Phase 2b trial of zelnecirnon in atopic dermatitis is expected in mid-2024.

Enrollment is progressing well in the Phase 2a trial of zelnecirnon in asthma.

Phase 2 data for tivumecirnon in combination with pembrolizumab in checkpoint-naïve non-small cell lung cancer was presented at SITC.

Total Revenue
$0
EPS
-$0.82
Previous year: -$0.63
+30.2%
Gross Profit
-$908K
Cash and Equivalents
$54.1M
Previous year: $27.7M
+95.4%
Free Cash Flow
-$22M
Previous year: -$17.2M
+27.4%
Total Assets
$200M
Previous year: $209M
-4.7%

RAPT

RAPT

Forward Guidance

RAPT Therapeutics anticipates continued clinical development progress and expects its current cash balance to support planned operations through mid-2025.

Positive Outlook

  • Anticipated reporting of top-line data from Phase 2b trial of zelnecirnon in atopic dermatitis in mid-2024.
  • Good progress in enrolling Phase 2a trial in asthma.
  • Strong cash balance expected to support planned operations through mid-2025.
  • Advancement of zelnecirnon in inflammatory diseases.
  • Advancement of tivumecirnon in oncology.

Challenges Ahead

  • Unexpected or unfavorable safety or efficacy data during clinical studies.
  • Lower than expected enrollment in Phase 2b clinical trial of zelnecirnon in AD.
  • Unanticipated or greater than anticipated impacts or delays due to macroeconomic conditions.
  • Changes in expected or existing competition.
  • Uncertainties and timing of the regulatory approval process.