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Mar 31

Gossamer Bio Q1 2025 Earnings Report

Gossamer Bio reported a narrowed net loss and recorded $9.9 million in collaboration revenue in Q1 2025.

Key Takeaways

In Q1 2025, Gossamer Bio reported $9.9 million in collaboration revenue and a net loss of $36.6 million, while continuing to advance its registrational studies for seralutinib. The company closed new patient screening for its Phase 3 PROSERA Study and maintains a strong cash position to fund operations into the first half of 2027.

Reported $9.9 million in collaboration revenue, including $6.6 million from cost reimbursements.

Net loss decreased to $36.6 million from $41.9 million in Q1 2024.

Cash and marketable securities totaled $257.9 million, expected to fund operations into H1 2027.

Patient screening closed for Phase 3 PROSERA Study; topline data expected in February 2026.

Total Revenue
$9.89M
0
EPS
-$0.16
Previous year: -$0.19
-15.8%
R&D Expenses
$38M
Previous year: $32.4M
+17.4%
G&A Expenses
$8.66M
Previous year: $9.57M
-9.5%
Wtd Avg Shares Used
226.82M
Previous year: 225.74M
+0.5%
Cash and Equivalents
$258M
Previous year: $244M
+5.5%
Total Assets
$281M
Previous year: $259M
+8.2%

Gossamer Bio

Gossamer Bio

Gossamer Bio Revenue by Segment

Forward Guidance

Gossamer expects to complete enrollment in the Phase 3 PROSERA Study in June 2025 and initiate the SERANATA Study in Q4 2025, while maintaining sufficient funding into the first half of 2027.

Positive Outlook

  • PROSERA Phase 3 patient screening closed; full enrollment expected in June 2025.
  • Topline data from PROSERA Phase 3 study anticipated in February 2026.
  • SERANATA Phase 3 study site activations planned for Q4 2025.
  • Collaboration with Chiesi advancing seralutinib development globally.
  • Sufficient cash runway projected through H1 2027.

Challenges Ahead

  • Ongoing operating losses driven by R&D and G&A expenses.
  • Total liabilities exceed total assets by $6.25 million.
  • Accumulated deficit surpassed $1.3 billion.
  • Continued reliance on successful outcomes from seralutinib trials.
  • Potential regulatory and trial execution risks remain for both PROSERA and SERANATA studies.