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Oncolytics Biotech Inc T.ONC

Alternate Symbol(s):  ONCY

Oncolytics Biotech Inc. is a clinical-stage 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 registration-enabling clinical 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 Noteableon Oct 26, 2023 8:40pm
340 Views
Post# 35703318

ONCY’s Phase 1b/2 mPC results compared over 2019 to 2023

ONCY’s Phase 1b/2 mPC results compared over 2019 to 2023
2019 vs 2021 vs 2023 results in ONCYs Phase 1b/2 pancreatic cancer studies are compared below first evaluating pelareorep in combination with pembrolizumab in advanced pancreatic cancer, and then, in ONCYs GOBLET Phase 1/2 clinical trial evaluating pelareorep in combination with atezolizumab + nab-paclitaxel in advanced/metastatic pancreatic cancer. 
https://d1io3yog0oux5.cloudfront.net/_317335d214f0f2271588d77471e4d933/oncolyticsbiotech/db/343/2239/pdf/Mahalingam+et+al%2C+EMSO+July+2015.pdf

The initial 2019 survival analysis for 33 patients in difficult-to-treat second line pancreatic cancer patients who were treated with pelareorep + pembrolizumab without chemotherapy resulted in one PR23 SD and five PD as best response, a median PFS of 4 months and a median OS of 10.2 months, with 1- and 2-year survival of 45% and 24%, respectively.
https://oncolyticsbiotech.com/press_releases/oncolytics-biotechr-announces-publication-of-positive-reo-024-study-results-for-pelareorep-in-combination-with-keytrudar-in-patients-with-advanced-pancreatic-adenocarcinoma/

The 2021 analysis of the 2019 Phase 1b/2  patients who were treated witpelareorep in combination with pembrolizumab demonstrated that 42% disease control was achieved in difficult-to-treat second line pancreatic cancer patients despite the absence of chemotherapy in the treatment regimen, witone patient achieviing a partial response and four patients achieviinstable disease. 

https://oncolyticsbiotech.com/press_releases/oncolytics-biotech-announces-clinical-and-biomarker-data-demonstrating-clinical-proof-of-concept-for-pelareorep-checkpoint-inhibitor-combination-in-pancreatic-cancer/
On October 16, 2023  the GOBLET Phase 1/2 metastatic pancreatic cancer abstract was released at ESMO and reported on results in patients who were treated with pelareorep + pembrolizumab + chemotherapy (nab-paclitaxel). Preliminary results were updated PDAC data showing a median PFS of 7.2 monthsinterim median overall survival of 10.6 months, expansion of both pre-existing and new T-cell clones and a 6-month survival rate of 82% in a patient population comprised of patients where 92% presented with metastatic disease, 69% in the liver - the worst of the worst - whichistorically only 10% survive longer than one (1) year.  
The results showed that of 13 evaluable patients had a partial response (PR) in a patient population whichistorically have not responded to in the past. A  partial response (PR) is defined as at least a 30% decrease in the sum of the target lesions.

This is the first time that any study demonstrated that a checkpoint inhibitor in any I/O combination showed effectiveness in the treatment of advanced/metastatic pancreatic cancer (PDAC) 
 
By comparision , a recently published phase I study of nivolumab and the anti-CC chemokine receptor 4 antibody mogamulizumab in patients with advanced solid tumors included 15 patients with PDAC. The authors reported 1 confirmed partial response and 2 unconfirmed partial responses in patients with PDAC.

In another study the observed efficacy of durvalumab plus tremelimumab therapy and durvalumab monotherapy in a 65 patient Phase 2 study reflective of a population of patients with mPDAC who had poor prognoses and rapidly progressing disease, the objective response rate was only 3.1%, and no patients (0.0%) responded to durvalumab monotherapy.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647002/

 
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