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Oncolytics Biotech Inc T.ONC

Alternate Symbol(s):  ONCY

Oncolytics Biotech Inc. is a biotechnology company. The Company is focused on developing pelareorep, an intravenously delivered immunotherapeutic agent that activates the innate and adaptive immune systems and weakens tumor defense mechanisms. This compound induces anti-cancer immune responses and promotes an inflamed tumor phenotype turning cold tumors hot through innate and adaptive immune responses to treat a variety of cancers. This improves the ability of the immune system to fight cancer, making tumors more susceptible to a broad range of oncology treatments. The Company’s primary focus is to advance its programs in hormone receptor-positive / human epidermal growth factor 2- negative (HR+/HER2-) metastatic breast cancer and advanced/metastatic pancreatic ductal adenocarcinoma to phase 3 licensure-enabling studies. In addition, it is exploring opportunities for registrational programs in other gastrointestinal cancers through its GOBLET platform study.


TSX:ONC - Post by User

Post by Geneman2004on Apr 29, 2023 1:24pm
1326 Views
Post# 35420914

ASCO relevance

ASCO relevanceLooking for grizzled veterans of this story. Are there additional discussion sites? Also posted on Stocktwits.

This ASCO presentation may spark a change in sentiment about the company. Seems like a good time to discuss ONCY if there is actual work being done on the story. You don't want to get over your skis on this ASCO presentation. BRACELET is a 3-arm trial with 15 patients in each - not designed to reveal a reliable survival outcome but powered to inform about response rate and immune impact. BRACELET has excluded ER- breast cancer patients - a group with no demonstrated response. The abstract was approved for presentation with data from NOV 2022; the ASCO data will be updated by 6 months. If the MAY 2023 BRACELET data confirm the results of the 57 ER+ patients in the IND213 trial (~30 Reo treated patients in BRACELET and IND213), the company negotiates with a partner and the FDA for a Ph III registration trial. If the updated BRACELET results are lukewarm, the breast indication is eliminated.
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