GigaGen Inc., a biotechnology company advancing transformative
antibody drugs for immune deficiencies, infectious diseases and
checkpoint resistant cancers, and a subsidiary of Grifols,
presented investigational new drug (IND)-enabling data and the
clinical trial design for its first-in-human Phase 1 study
evaluating the company’s oncology candidate, GIGA-564, at the 2023
Society for Immunotherapy of Cancer (SITC) Annual Meeting.
The comprehensive dataset from non-clinical models continues to
demonstrate GIGA-564’s potential to improve outcomes for cancer
patients through weak checkpoint inhibition of CTLA-4. GIGA-564
depletes intratumoral T regulatory cells (Tregs) within the tumor
microenvironment, which enables the tumor-killing activity of
cytotoxic T cells. Results also show that GIGA-564 offers increased
anti-tumor efficacy and reduced toxicity compared to the
commercially available drug ipilimumab, a monoclonal antibody
designed to work through CTLA-4 checkpoint inhibition.
The Phase 1a/1b dose escalation and dose-expansion trial,
expected to start in 2024, will evaluate GIGA-564 for the treatment
of advanced solid tumors. The trial will be conducted by National
Cancer Institute (NCI) researchers in close partnership with the
GigaGen team, as established in the recently signed CRADA between
GigaGen and NCI, a part of the National Institutes of Health.
“We are pleased to present the design of this first-in-human
Phase 1 trial for GIGA-564,” said Erica Stone, vice president of
Oncology at GigaGen. “GIGA-564’s weak CTLA-4 blockade
differentiates the drug candidate from any other anti-CTLA-4 agent.
We look forward to potentially translating the promising efficacy
and safety profiles observed in preclinical models into the clinic
and demonstrating its potential to improve the treatment landscape
for patients with solid malignancies.”
About GIGA-564GIGA-564, a fully human
monoclonal antibody, distinguishes itself from currently available
anti-CTLA-4 drugs. Previous anti-CTLA-4 drugs were designed to
strongly block CTLA-4's interaction with its ligands, thereby
enhancing T cell co-stimulation. However, this approach has been
associated with heightened immune-related side effects. Moreover,
recent insights reveal that previous anti-CTLA-4 drugs contribute
to an increased proliferation of T regulatory cells (Tregs), which
may dampen their intended effect of activating cytotoxic T cells
that are vital for attacking tumors. In comparison, GIGA-564's
uniqueness stems from its minimal CTLA-4 blockade and its ability
to deplete intratumoral Tregs within the tumor
microenvironment.
About GrifolsGrifols is a global healthcare
company founded in Barcelona in 1909 committed to improving the
health and well-being of people around the world. A leader in
essential plasma-derived medicines and transfusion medicine, the
company develops, produces, and provides innovative healthcare
services and solutions in more than 110 countries.
Patient needs and Grifols’ ever-growing knowledge of many
chronic, rare and prevalent conditions, at times life-threatening,
drive the company’s innovation in both plasma and other
biopharmaceuticals to enhance quality of life. Grifols is focused
on treating conditions across a broad range of therapeutic areas:
immunology, hepatology and intensive care, pulmonology, hematology,
neurology, and infectious diseases.
A pioneer in the plasma industry, Grifols continues to grow its
network of donation centers, the world’s largest with over 390
across North America, Europe, Africa and the Middle East, and
China.
As a recognized leader in transfusion medicine, Grifols offers a
comprehensive portfolio of solutions designed to enhance safety
from donation to transfusion, in addition to clinical diagnostic
technologies. It provides high quality biological supplies for
life-science research, clinical trials, and for manufacturing
pharmaceutical and diagnostic products. The company also supplies
tools, information and services that enable hospitals, pharmacies
and healthcare professionals to efficiently deliver expert medical
care.
Grifols, with more than 24,000 employees in more than 30
countries and regions, is committed to a sustainable business model
that sets the standard for continuous innovation, quality, safety,
and ethical leadership.
In 2022, Grifols’ economic impact in its core countries of
operation was EUR 9.6 billion. The company also generated 193,000
jobs, including indirect and induced.
The company’s class A shares are listed on the Spanish Stock
Exchange, where they are part of the Ibex-35 (MCE:GRF). Grifols
non-voting class B shares are listed on the Mercado Continuo
(MCE:GRF.P) and on the U.S. NASDAQ through ADRs
(NASDAQ:GRFS).GigaGen is advancing transformative antibody drugs
for immune deficiency, infectious diseases and checkpoint resistant
cancers by leveraging industry-leading, single-cell technologies.
Its novel technology platforms uniquely capture and recreate
complete immune repertoires as functional antibody libraries. This
approach has enabled the creation of first-in-class recombinant
polyclonal antibody therapies for the treatment of infectious
diseases. In addition, GigaGen’s lead oncology asset, GIGA-564, is
an anti-CTLA-4 monoclonal antibody that has demonstrated improved
anti-tumor efficacy and reduced toxicities in preclinical models
through a unique mechanism of action.
For more information, please
visit www.grifols.com or www.gigagen.com.
Media Contacts:Monica Rouco Molina, Ph.D.
LifeSci Communicationsmroucomolina@lifescicomms.com Tel:
+1-929-469-3850
Grifols Press Officemedia@grifols.comTel. +34
93 571 00 02
LEGAL DISCLAIMER
The facts and figures contained in this report
that do not refer to historical data are “future projections and
assumptions”. Words and expressions such as “believe”, “hope”,
“anticipate”, “predict”, “expect”, “intend”, “should”, “will seek
to achieve”, “it is estimated”, “future” and similar expressions,
in so far as they relate to the Grifols group, are used to identify
future projections and assumptions. These expressions reflect the
assumptions, hypotheses, expectations and predictions of the
management team at the time of writing this report, and these are
subject to a number of factors that mean that the actual results
may be materially different. The future results of the Grifols
group could be affected by events relating to its own activities,
such as a shortage of supplies of raw materials for the manufacture
of its products, the appearance of competitor products on the
market, or changes to the regulatory framework of the markets in
which it operates, among others. At the date of compiling this
report, the Grifols group has adopted the necessary measures to
mitigate the potential impact of these events. Grifols, S.A. does
not accept any obligation to publicly report, revise or update
future projections or assumptions to adapt them to events or
circumstances subsequent to the date of writing this report, except
where expressly required by the applicable legislation. This
document does not constitute an offer or invitation to buy or
subscribe shares in accordance with the provisions of the following
Spanish legislation: Royal Legislative Decree 4/2015, of 23
October, approving recast text of Securities Market Law; Royal
Decree Law 5/2005, of 11 March and/or Royal Decree 1310/2005, of 4
November, and any regulations developing this legislation. In
addition, this document does not constitute an offer of purchase,
sale or exchange, or a request for an offer of purchase, sale or
exchange of securities, or a request for any vote or approval in
any other jurisdiction. The information included in this document
has not been verified nor reviewed by the external auditors of the
Grifols group.
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