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Oncolytics Biotech® Announces Presentation at the Society for Immunotherapy of Cancer 2018 Annual Meeting Showcasing Upregulation of PD-L1 Expression with Reovirus Infection

Key Takeaway: Oncolytics Biotech announced that data presented at the SITC 2018 Annual Meeting demonstrates its oncolytic virus, pelareorep, can upregulate PD-L1 expression in prostate cancer cells. This finding suggests that pelareorep may enhance the effectiveness of immune checkpoint inhibitors, potentially improving treatment outcomes for patients with traditionally difficult-to-treat prostate cancers. The study highlights the importance of combining oncolytic virotherapy with immunotherapy.

Market Sentiment Analysis

POSITIVE FACTORS

  • Pelareorep shows promise in enhancing immune responses in prostate cancer.
  • The study validates the combination of oncolytic virotherapy with checkpoint inhibitors.
  • Oncolytics Biotech is advancing its clinical development program effectively.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+48%
120-day peak, hindsight
Typical move
7%
average across 3 past catalysts
Cash runway
~1 mo
High dilution risk
Lead asset
REOLYSIN
Phase 3 · Carcinoma, Squamous Cell of the Head and Neck

Full Press Release Details

- Oncolytic virus enhances immune checkpoint inhibitor response in prostate cancers -

CALGARY, Alberta and SAN DIEGO, Nov. 09, 2018 (GLOBE NEWSWIRE) -- Oncolytics Biotech®Inc. (NASDAQ: ONCY) (TSX: ONC), currently developing pelareorep, an intravenously delivered immuno-oncolytic virus, today announced that data will be presented demonstrating pelareorep’s ability to upregulate PD-L1 during infection of prostate cancer cells. The presentation is taking place at the Society for Immunotherapy of Cancer (SITC) 2018 Annual Meeting, November 7-11 in Washington, D.C.
The presentation, authored Dr. Hardev Pandha, Professor of Medical Oncology, the University of Surrey, et al., is titled "Reovirus infection of prostate cancer induces upregulation of the negative regulators PD-L1 and BTLA”.
“This study has clearly confirmed that oncolytic virotherapy is able to create an inflamed phenotype and sensitize the tumor to immune checkpoint blockade,” said Dr. Pandha. “The proinflammatory effects of viral oncolysis may stem from its attraction and activation of natural killer cells, which through the production of chemokines in the tumour, control the levels of stimulatory dendritic cells. This then primes the effector T-cells, increasing the responsiveness of prostate tumours to anti-PD-1 immunotherapy.”
Prostate cancers are typically immunologically “cold” tumors, making it difficult to treat this patient population with checkpoint inhibitors due to the non-inflamed tumor type. The study outlines the effectiveness of using oncolytic viral therapy for prostate cancers could be improved with the targeted blockade of PD-1 and CD73. In testing anti-PD-1 and anti-CD73 blockade as a monotherapy and in combination with reovirus therapy, the study validates that oncolytic virotherapy is able to “heat up” the prostatic tumor microenvironment, ultimately sensitizing this area to immune checkpoint blockade and increasing the responsiveness of prostate tumors to anti-PD-1 immunotherapy.
“While prostate cancers are a notoriously difficult indication to treat with immunotherapy, our study showcases how pelareorep can improve the efficacy and responsiveness of checkpoint inhibitors in these hard-to-treat cancers,” said Dr. Matt Coffey, President and Chief Executive Officer of Oncolytics Biotech. “Ultimately, in upregulating expression of PD-L1 and BTLA, our results demonstrate the ways that pelareorep – and oncolytic viruses more broadly – are an optimal combination therapy. These results further validate our interest in immune checkpoint inhibitors, our clinical plans and our business development strategy.”
Additional details can be found on the company website: www.oncolyticsbiotech.com/technology/posters-publications.
Presentation Number: P597
Title: Reovirus infection of prostate cancer induces upregulation of the negative regulators PD-L1 and BTLA
Date: Friday, November 9
Lecture Time: 12:30 p.m. – 2:00 p.m. and 6:30 p.m. – 8:00 p.m.
Location: Hall E
Speakers: Dr. Nicola Annels
Session: Oncolytic Viruses and Intratumoral Therapies
About PelareorepPelareorep is a non-pathogenic, proprietary isolate of the unmodified reovirus: a first-in-class intravenously delivered immuno-oncolytic virus for the treatment of solid tumors and hematological malignancies. The compound induces selective tumor lysis and promotes an inflamed tumor phenotype through innate and adaptive immune responses to treat a variety of cancers and has been demonstrated to be able to escape neutralizing antibodies found in patients.
About Oncolytics Biotech Inc.Oncolytics is a biotechnology company developing pelareorep, an intravenously delivered immuno-oncolytic virus. The compound induces selective tumor lysis and promotes an inflamed tumor phenotype -- turning "cold" tumors "hot" -- through innate and adaptive immune responses to treat a variety of cancers. Oncolytics' clinical development program emphasizes three pillars: chemotherapy combinations to trigger selective tumor lysis and immuno-therapy and immune modulator (IMiD) combinations to produce innate and adaptive immune responses. Oncolytics is currently conducting and planning additional studies in combination with checkpoint inhibitors and targeted and IMiD therapies in solid and hematological malignancies, as it prepares for a phase 3 registration study in metastatic breast cancer. For further information, please visit: www.oncolyticsbiotech.com.
This press release contains forward-looking statements, within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended and forward-looking information under applicable Canadian securities laws (such forward-looking statements and forward-looking information are collectively referred to herein as “forward-looking statements”). Forward-looking statements, including the Company's belief as to the potential and mode of action of REOLYSIN, also known as pelareorep, as a cancer therapeutic; and other statements related to anticipated developments in the Company's business and technologies involve known and unknown risks and uncertainties, which could cause the Company's actual results to differ materially from those in the forward-looking statements. Such risks and uncertainties include, among others, the availability of funds and resources to pursue research and development projects, the efficacy of pelareorep as a cancer treatment, the success and timely completion of clinical studies and trials, the Company's ability to successfully commercialize pelareorep, uncertainties related to the research and development of pharmaceuticals, uncertainties related to the regulatory process and general changes to the economic environment. Investors should consult the Company's quarterly and annual filings with the Canadian and U.S. securities commissions for additional information on risks and uncertainties relating to the forward-looking statements. Investors are cautioned against placing undue reliance on forward-looking statements. The Company does not undertake to update these forward-looking statements, except as required by applicable laws.
Company ContactMichael MooreVice President, Investor Relations & Corporate Communications858-886-7813mmoore@oncolytics.ca
Investor RelationsRobert UhlWestwicke Partners858-356-5932robert.uhl@westwicke.com Media ContactJason SparkCanale Communications619-849-6005jason@canalecomm.com

Frequently Asked Questions

What is pelareorep?

Pelareorep is an intravenously delivered immuno-oncolytic virus developed by Oncolytics Biotech.

What was presented at the SITC 2018 Annual Meeting?

Data showing pelareorep's ability to upregulate PD-L1 expression in prostate cancer cells.

How does pelareorep affect prostate cancer treatment?

It enhances the effectiveness of immune checkpoint inhibitors, making tumors more responsive.

Who authored the study on pelareorep?

The study was authored by Dr. Hardev Pandha and colleagues from the University of Surrey.

Last updated: Nov 9, 2018