Oncolytics Biotech Inc. announced the submission of a Type C meeting request to the FDA. This meeting aims to discuss the Company's planned registration-enabling trial for pelareorep in HR+ HER2- metastatic breast cancer (mBC). A key focus for Oncolytics in 2024 is defining the regulatory path for pelareorep in breast cancer treatment.

The company are optimistic that pelareorep, in combination with paclitaxel, could significantly enhance clinical outcomes for patients with HR+ HER2- metastatic breast cancer. The company position is strengthened by encouraging data from two randomized studies (BRACELET-1 and IND-213) and the AWARE-1 study, paving the way for the next phase of pelareorep's development and its registration.