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Oncolytics Biotech (ONCY) investor relations material
Oncolytics Biotech Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Transitioning from proof-of-concept to regulatory clarity for pelareorep, focusing on registration-enabling studies in first-line metastatic pancreatic ductal adenocarcinoma (mPDAC).
New CEO and Chief Business Officer appointed, both with significant biotech transaction experience.
Pelareorep shows ability to convert immunologically "cold" tumors to "hot," enhancing immune response and survival in mPDAC and breast cancer.
Strategic prioritization of mPDAC program based on compelling survival and translational data, with regulatory discussions underway.
Financial highlights
Cash and cash equivalents of $14.6 million as of June 30, 2025, with projected runway into Q1 2026.
Net loss for Q2 2025 was $6.2 million, improved from $7.3 million in Q2 2024; loss per share was $0.07 vs. $0.10 year-over-year.
R&D expenses for Q2 2025 were $2.8 million, down from $4.6 million in Q2 2024, reflecting focus on GOBLET study.
General and administrative expenses decreased to $2.9 million from $3.4 million year-over-year.
Net cash used in operating activities for the first half of 2025 was $12.0 million, down from $14.3 million in the same period of 2024.
Outlook and guidance
Updated clinical timeline for registration-enabling pivotal study in 1L mPDAC expected in Q3 2025.
Start-up activities for pivotal study anticipated as early as Q4 2025, pending regulatory feedback.
Updated safety and efficacy data for GOBLET study Cohort 4 in anal carcinoma expected by end of 2025.
Initial responses from the U.S. PTO on patent extension for pelareorep expected in Q4 2025.
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