GigaGen Inc., a biotechnology company advancing transformative
antibody drugs for immunodeficiencies, infectious diseases and
checkpoint-resistant cancers, and a subsidiary of Grifols,
announced today that it has been awarded a contract by the
Biomedical Advanced Research and Development Authority (BARDA),
part of the Administration for Strategic Preparedness and Response
(ASPR) within the U.S. Department of Health and Human Services
(HHS). The award, valued at up to $135.2 million, is to develop a
recombinant polyclonal antibody therapy for botulinum neurotoxins
(BoNT) and a second biothreat of interest to the agency that will
be determined at a later time.
“We are thrilled to have been awarded this BARDA contract and
are proud to continue our collaboration with the U.S. government to
advance innovative therapies against naturally emerging and
intentional biological threats,” said Carter Keller, senior vice
president of Grifols and head of GigaGen. “GigaGen aims to change
the way infectious diseases are treated with the world’s only
recombinant polyclonal antibody therapeutic platform. Building on
our successful collaboration with the Department of Defense (DOD),
this project demonstrates the versatility of our recombinant
polyclonal antibody platform, which is ideally suited for rapid
responses to imminent biological threats.”
The BARDA project builds upon GigaGen’s contract awarded by the
U.S. DOD Joint Program Executive Office for Chemical, Biological,
Radiological and Nuclear Defense (JPEO-CBRND) in 2022. The DOD
project demonstrated the utility of GigaGen’s first-in-class
recombinant human polyclonal antibody discovery platform against
biological threats, focusing on two BoNT variants. Following
success in this program that included in vivo neutralization of the
two botulinum neurotoxins, the BARDA project will support the
manufacturing and initial clinical development of a drug product
that targets all seven BoNT variants. BoNT, one of the most toxic
biological substances, is produced by the bacterium Clostridium
botulinum and can cause progressive muscle paralysis from the head
to the rest of the body, which can be fatal if left untreated.
GigaGen recently received clearance from the U.S. Food and Drug
Administration (FDA) for its Investigational New Drug (IND)
application to initiate a Phase 1 clinical trial to evaluate the
company’s first recombinant polyclonal antibody therapeutic for the
treatment of hepatitis B virus (HBV) infection, GIGA-2339. The
company anticipates initiating the trial in Q4 2024.
This project has been funded in whole or in part with federal
funds from the Department of Health and Human Services;
Administration for Strategic Preparedness and Response; Biomedical
Advanced Research and Development Authority, under contract number
75A50124C00049.
About GigaGen’s platformGigaGen’s
next-generation recombinant polyclonal platform offers a novel way
to develop synthetic polyclonal antibody therapeutics in the
laboratory, which are potentially more powerful than what a natural
immune response can provide. Using high-throughput, single-cell
genomic and protein engineering technology, GigaGen creates cell
lines that express recombinant human antibodies against a diversity
of infectious disease antigens. The polyclonal cell bank can then
be used to continuously manufacture recombinant polyclonal products
against the pathogen of interest at existing manufacturing
facilities. GigaGen has demonstrated that its products are hundreds
of times more potent than plasma-derived antibody therapies. They
replicate and enhance the natural antibody diversity, encompassing
thousands of antibodies. This offers a significant advantage over
monoclonal antibody therapies, as they can address the vast
diversity of circulating pathogen variants and help prevent immune
escape upon pathogen mutation.
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. The company 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.
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
immunodeficiencies, 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:Michael RubensteinLifeSci
Communicationsmrubenstein@lifescicomms.comTel: +1- 561-289-7981
Grifols Press Officemedia@grifols.comTel. +34
93 571 00 02
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