Imugene Announces Clinical Trial Supply Agreement with Merck KGaA, Darmstadt, Germany and Pfizer to Evaluate HER-Vaxx in Combination with Avelumab for Treatment of Gastric Cancer
17 November 2021 - 5:05PM
Imugene (ASX: IMU) today announced a new clinical trial supply
agreement with Merck KGaA, Darmstadt, Germany (ETR: MRK) and
Pfizer Inc. (NYSE: PFE) to evaluate the safety and efficacy of
Imugene’s HER-Vaxx, a B-cell activating immunotherapy, in
combination with avelumab, an immune checkpoint inhibitor targeting
PD-L1, in patients with HER-2 positive gastric cancer. Avelumab,
which is marketed as BAVENCIO®, is co-developed and
co-commercialized by Merck KGaA, Darmstadt, Germany and Pfizer Inc.
neoHERIZON is an open-label, multi-center, randomized, Phase 2
clinical trial designed to assess the safety and efficacy of
perioperative HER-Vaxx combined with chemotherapy with or without
avelumab compared to chemotherapy alone in patients with HER-2
positive gastric or gastroesophageal junction
adenocarcinomas. The study’s primary endpoint is pathologic
complete response. Secondary endpoints include safety and biomarker
evaluation.
“We are very excited for the opportunity to treat patients with
this new generation of HER-2 targeted B-cell immunotherapy,
which has the potential to address significant unmet need
in early HER-2 overexpressing gastric cancer that
remains a challenging indication with poor prognosis. The
combination of chemotherapy and HER-Vaxx alone or in combination
with avelumab in this type of gastric cancer may support a better
treatment outcome for patients,” said Dirk Arnold M.D., Ph.D.,
Director of the Asklepios Tumorzentrum in Hamburg.
“Imugene is excited to announce this collaboration with Merck
KGaA, Darmstadt, Germany and Pfizer. HER-Vaxx has shown a tolerable
safety profile and encouraging efficacy in patients with metastatic
HER-2 positive gastric cancer, and we are looking forward to
evaluating HER-Vaxx with avelumab in the perioperative clinical
setting,” said Leslie Chong, Managing Director & Chief
Executive Officer of Imugene. “Working together, we’re committed to
finding ways to address the unmet needs of patients living with
cancer.”
Effective immediately, under the terms of the agreement, Imugene
will be the sponsor of the study and will fund the clinical study
from existing budgets and resources. Merck KGaA, Darmstadt, Germany
and Pfizer will provide avelumab for the duration of the study.
About Gastric and Gastro-esophageal Cancer
Perioperative (pre- and post-surgery) treatment in gastric or
gastro-esophageal cancer remains an unmet need for patients with
HER-2 positive tumours. The current standard of care is limited to
chemotherapy, radiotherapy, and surgery when gastric cancer is
diagnosed in its early stages. Immune checkpoint inhibitors have
been successfully introduced to metastatic gastric cancer. Moving
HER-Vaxx into earlier gastric cancer in combination with
chemotherapy or an immune checkpoint inhibitor may improve
treatment outcomes for patients with this difficult to treat
cancer.
About HER-Vaxx
Imugene’s HER-Vaxx is a B-cell peptide cancer immunotherapy
designed to treat tumours that over-express the HER-2/neu receptor,
such as gastric, breast, ovarian, lung and pancreatic cancers. The
immunotherapy is constructed from several B cell epitopes derived
from the extracellular domain of HER-2/neu. It has been shown in
pre-clinical studies and in Phase 1 and 2 studies to stimulate a
potent polyclonal antibody response to HER-2/neu, a well-known and
validated cancer target.
For more information please contact:
Leslie
Chong Managing
Director and Chief Executive Officerinfo@imugene.com
Investor Enquiriesinvestor@imugene.com
Media EnquiriesMatt Wright
matt@nwrcommunications.com.au
Follow us on Twitter @TeamImugeneLike us on Facebook
@ImugeneConnect with us on LinkedIn @Imugene Limited
About Imugene (ASX:IMU)
Imugene is a clinical stage immuno-oncology
company developing a range of new and novel immunotherapies that
seek to activate the immune system of cancer patients to treat and
eradicate tumours. Our unique platform technologies seek to harness
the body’s immune system against tumours, potentially achieving a
similar or greater effect than synthetically manufactured
monoclonal antibody and other immunotherapies. Our product pipeline
includes multiple immunotherapy B-cell vaccine candidates and an
oncolytic virotherapy (CF33) aimed at treating a variety of cancers
in combination with standard of care drugs and emerging
immunotherapies such as CAR T’s for solid tumours. We are supported
by a leading team of international cancer experts with extensive
experience in developing new cancer therapies with many approved
for sale and marketing for global markets.
Our vision is to help transform and improve the
treatment of cancer and the lives of the millions of patients who
need effective treatments. This vision is backed by a growing body
of clinical evidence and peer-reviewed research. Imugene is well
funded and resourced, to deliver on its commercial and clinical
milestones. Together with leading specialists and medical
professionals, we believe Imugene’s immuno-oncology therapies will
become foundation treatments for cancer. Our goal is to ensure that
Imugene and its shareholders are at the forefront of this rapidly
growing global market.
Release authorised by the Managing Director and
Chief Executive OfficerImugene Limited, Level 3, 62 Lygon Street,
Carlton, VIC, 3053, Australia
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