Oncolytics Biotech® Announces First Patient Treated in Phase 2 Study Combining Pelareorep and Keytruda® in Advanced Pancrea...
26 Noviembre 2018 - 7:00AM
Oncolytics Biotech® Inc. (NASDAQ: ONCY) (TSX: ONC), currently
developing pelareorep, an intravenously delivered immuno-oncolytic
virus, today announced that the first patient was treated in a
phase 2 study combining pelareorep with Merck’s Keytruda® to treat
advanced pancreatic adenocarcinoma. The primary objective of the
study is to determine the overall response rate (ORR) by iRECIST
criteria. Secondary objectives include safety of the
combination, immune response as determined by analysis of pre- and
post-treatment biopsies and blood-based immune markers,
determination of progression-free survival (PFS) by iRECIST
criteria; and one-year, two-year and median overall survival (OS).
“We are very excited to start enrollment in this
combination study which expands upon our findings from an earlier
Keytruda study in advanced pancreatic cancer,” said Dr. Matt
Coffey, President and Chief Executive Officer of Oncolytics
Biotech. “REO 024, our previous phase 1b study with Keytruda,
showed objective response, long-term stabilization of disease and
promotion of an inflamed phenotype in second line pancreatic cancer
patients. This new phase two study should corroborate anti-tumor
activity and potentially confirm predictive biomarkers laying the
groundwork towards our goal of becoming a standardized backbone for
checkpoint inhibitors.”
This study is a phase 2, single arm, open-label
study enrolling up to 30 patients with advanced pancreatic
adenocarcinoma who experienced disease progression or did not
tolerate first-line therapy. The principal investigator is Dr.
Devalingham Mahalingam, of Northwestern University. The first 16
patients will be enrolled in stage one, and up to 14 additional
patients will be enrolled in stage two if pre-specified criteria
are met. The pre-defined criteria state that, for the primary
objective, three or more responses out of 16 are needed in stage
one to continue the trial to the full 30 patients.
For more information about the study, including
a comprehensive list of inclusion and exclusion criteria, please
visit: www.clinicaltrials.gov (identifier:
NCT03723915).
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 Partners858-356-5932
robert.uhl@westwicke.com |
Media
ContactJason SparkCanale Communications 619-849-6005
jason@canalecomm.com |
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