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Traws Pharma (TRAW) investor relations material
Traws Pharma Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Cash and cash equivalents were $6.4 million as of September 30, 2025, with an accumulated deficit of $632.5 million.
Substantial doubt exists about the ability to continue as a going concern for more than one year without additional funding.
Advanced Phase 2 studies for ratutrelvir, a ritonavir-free protease inhibitor for acute and Long COVID, with topline data expected by year-end 2025.
The company is a clinical-stage biopharmaceutical firm with four clinical programs, focusing on respiratory viral diseases and cancer.
Recent developments include the acquisition of assets from Viriom and the termination of a license agreement with Symbio.
Financial highlights
Net income for the nine months ended September 30, 2025, was $16.6 million, compared to a net loss of $136.6 million for the same period in 2024.
Revenue for the nine months ended September 30, 2025, was $2.8 million, up from $0.2 million in 2024, mainly due to the recognition of deferred revenue from the terminated Symbio agreement.
Operating expenses for the nine months ended September 30, 2025, were $13.3 million, down from $137.3 million in 2024, reflecting a significant decrease in acquired in-process R&D expenses.
R&D expenses decreased to $2.3 million for Q3 2025 from $5.1 million year-over-year, and G&A expenses fell to $1.7 million from $3.5 million.
Net loss for Q3 2025 was $4.0 million ($0.34 per share), improved from $8.5 million ($1.49 per share) in Q3 2024.
Outlook and guidance
The company expects to incur significant expenses and operating losses for the foreseeable future as it continues clinical development and seeks regulatory approvals.
Topline Phase 2 data for ratutrelvir expected by year-end 2025.
Management is exploring various funding sources, including equity, debt, and strategic partnerships, but there is no assurance of success.
Research and development expenditures are expected to increase as the TRX01 study progresses.
Actively seeking partnerships for legacy oncology assets to support further development.
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