Avigan(R) Shows Promising Results in Treatment of COVID Patients in Japan
PR85757
DUBAI, UAE, September 23, 2020, /PRNewswire=KYODO JBN/--
Completed Phase 3 clinical study paves way for approval request
Healthcare solutions provider Global Response Aid (GRA) and Dr. Reddy's
Laboratories (NYSE: RDY) announced that the anti-viral drug Avigan(R) produced
promising results in a single-blinded, placebo-controlled Phase 3 clinical
study conducted in Japan with the sponsorship of FujiFilm Toyama Chemical.
Patients who received Avigan(R) recovered from COVID-19 symptoms 2.8 days
earlier, on average, compared with the control group. Analysis showed patients
had a statistically significant higher probability to recover when administered
Avigan(R) compared with the patients not receiving the drug.
The study involved 156 hospitalized patients showing COVID-19 induced
pneumonia, and divided in two groups or "arms." Patients in the first arm
received Avigan(R). Patients in the second arm received a placebo looking
identical to the drug. A statistically significant percentage of the patients
in the group receiving Avigan(R) had a rapid reduction in viral loads.
The study aimed to measure recovery from pneumonia and COVID-19 symptoms. It
monitored patients' temperature, oxygen saturation and CT scan imaging of the
lungs. Time-to-alleviation of the symptoms was measured between the first
administration of the drug (or placebo) and the moment when SARS-COV-2 induced
symptoms became undetectable.
Shortening recovery time lowers the risk of complications in patients and,
importantly, significantly reduces the risk that a patient will spread the
virus. The latest results open the possibility of treating patients with mild
or moderate cases of COVID-19 in outpatient settings, which also could help
slow the spread of the pandemic.
Avigan(R), which contains the active ingredient Favipiravir, was developed by
FujiFilm Toyama Chemical in the 1990s as an anti-influenza drug. GRA, Dr.
Reddy's Laboratories, and FujiFilm Toyama recently entered a global licensing
agreement covering the production, marketing and distribution of Avigan(R).
Results of the Japan trial suggest the effectiveness of Avigan(R) as a
treatment to prevent COVID-19 patients from progressing from mild to more
severe or critical clinical stages of the disease, and to accelerate recovery
from COVID-19 symptoms.
GRA CEO Mitch Wilson said the FujiFilm Toyama study represents a breakthrough
in the fight against COVID-19, and opens the way for approval of Avigan(R) as a
COVID-19 treatment in Japan. The drug is already approved in India, Russia,
Indonesia and other countries around the world.
"The findings from this university-led study are the proof we all need to
tackle this pandemic," Wilson said. "We are actively working with regulators in
order to speed up the approval in major markets. Because Avigan(R) is
manufactured in pill form the drug can be self-administered from home, which
reduces patient load in hospitals and on medical staff. Furthermore Avigan(R)
does not require refrigerated transport or storage making it much easier to
quickly distribute the drug to countries and markets with limited cold storage
infrastructure"
Avigan(R) is the subject of clinical trials in COVID-19 patients in several
countries. It was used to treat COVID-19 patients in studies in China's Hubei
province, led by the China-Japan Friendship Hospital. It is undergoing testing
in the United States in a multi-site Phase 2 study involving initially hospitalized
patients, a trial sponsored by FujiFilm Toyama Chemical. It also is the subject of
an investigator-initiated Phase 2 study in subjects with mild or asymptomatic
COVID-19 being conducted by the Stanford University School of Medicine.
Avigan(R) Tablet was approved for manufacture and sale in Japan in 2014 as an
influenza anti-viral drug. The drug is to be considered for use only when there
is an outbreak of novel or re-emerging influenza virus infections in which
other influenza anti-viral drugs are either not effective or insufficiently
effective, and the Japanese government decides to use the drug as a
countermeasure against such influenza viruses.
GRA is a Dubai-based company established by global logistics leader Agility
(KSE: AGLTY) and AiPHARMA a biotechnology company to procure and develop
certified diagnostic, testing and protective products and services used in the
detection, treatment and prevention of COVID-19 and other public health threats.
About Global Response Aid (GRA)
Global Response Aid, based in Dubai, provides solutions to public health
challenges. GRA was established by global logistics leader Agility and AiPHARMA
a biotechnology company to procure and develop certified diagnostic, testing
and protective products and services used in the detection, treatment and
prevention of COVID-19 and other public health threats. GRA works with trusted
manufacturers to source safe, effective products for governments, health
authorities and public institutions; frontline medical facilities; NGOs; and
companies looking to safeguard workers and workplaces. GRA-sourced products
include ventilators, thermal detection equipment, thermometers, masks, goggles,
protective suits, nitrile gloves, cleaning and sanitation supplies, and
point-of-care test kits. GRA's mobile phone app helps stop the spread of
viruses through the use of community-driven contact tracing and alerts. GRA
also deploys Mobile Diagnostic Testing Vehicles and trained teams that perform
COVID-19 testing at schools and workplaces.
For more information, please visit https://globalresponseaid.com/
About FUJIFILM
FUJIFILM Toyama Chemical Co., Ltd. conducts the research, development,
manufacture, and sales of radiopharmaceuticals and small molecule
pharmaceutical products. Under close cooperation with FUJIFILM Corporation, it
aims to develop innovative diagnostic and therapeutic radiopharmaceuticals, as
well as therapeutic drugs having unique mechanisms of action in the fields of
"oncology," "central nervous system diseases," and "infectious diseases" where
significant unmet medical needs still exist. It also works to develop new
medicines utilizing drug delivery system (DDS) technologies, designed to
deliver the required amount of a drug in a timely manner to the specific body
area. By exploring synergy with in vitro diagnostic devices and reagents owned
by Fujifilm group companies, the company will expand its offering of
comprehensive solutions from diagnosis to treatment. FUJIFILM Toyama Chemical
have expanded its business areas to medical IoT solutions including a system to
support pharmacists' drug dispensing auditing work, and a transportation device
that enables strict temperature control suited for blood products, cells and
tissue used for regenerative medicine. Through the development and supply of
high-quality, high added-value new drugs and products that support the clinical
settings, FUJIFILM Toyama Chemical strives to solve various social challenges,
and contribute to improving medicine and enhancing the quality of life.
For more information, please visit http://fftc.fujifilm.co.jp/en/
About Dr. Reddy's
About Dr. Reddy's: Dr. Reddy's Laboratories Ltd. (BSE: 500124, NSE: DRREDDY,
NYSE: RDY) is an integrated pharmaceutical company, committed to providing
affordable and innovative medicines for healthier lives. Through its three
businesses - Pharmaceutical Services & Active Ingredients, Global Generics and
Proprietary Products – Dr. Reddy's offers a portfolio of products and services
including APIs, custom pharmaceutical services, generics, biosimilars and
differentiated formulations. Our major therapeutic areas of focus are
gastrointestinal, cardiovascular, diabetology, oncology, pain management and
dermatology. Dr. Reddy's operates in markets across the globe. Our major
markets include – USA, India, Russia & CIS countries, and Europe.
For more information, log on to: www.drreddys.com
About AiPharma
AiPHARMA is an early-stage biotechnology company with regional offices in
Boston, Dubai, Tokyo, Singapore and Hong Kong. Aipharma take a highly
interdisciplinary approach to science, with services building upon work from
leading academic labs in biophysics and algorithmic design that enables the
acceleration of life science research and development in the pursuit of
improved human health. The company leverages machine learning and automation to
build platforms for science at scale. With its foundations in engineering
disciplines, the company's platform technologies vertically integrate
proprietary hardware, software, bioinformatics, chemistries, and molecular
biology to advance basic research, target validation, and clinical trials.
For more information, log on to: www.aipharmalab.com
About Agility
Agility is a global logistics company with $5.2 billion in annual revenue and
26,000+ employees in more than 100 countries. It is one of the world's top
freight forwarding and contract logistics providers, and a leader and investor
in technology to enhance supply chain efficiency. Agility is a pioneer in
emerging markets and one of the largest private owners and developers of
warehousing and light industrial parks in the Middle East, Africa and Asia.
Agility's subsidiary companies offer fuel logistics, airport services,
commercial real estate and facilities management, customs digitization, and
remote infrastructure services.
For more information about Agility, visit www.agility.com
Twitter: twitter.com/agility
LinkedIn: linkedin.com/company/agility
YouTube: youtube.com/user/agilitycorp
Forward Looking Statement -- This news release includes forward-looking
statements, within the meaning of the Private Securities Litigation Reform Act
of 1995 that are subject to risks, uncertainties and other factors, including
the possibility of unfavorable results from clinical trials involving Avigan®
and the possibility that we may be unable to complete one or more of such
trials in the currently anticipated timelines or at all. Further, it is
possible that GRA and Dr. Reddy's may make a strategic decision to discontinue
development of Avigan®. As a result, Avigan® may never be successfully
commercialized. All statements other than statements of historical fact are
statements that could be deemed forward-looking statements. These risks,
uncertainties and other factors could cause actual results to differ materially
from those referred to in the forward-looking statements. The reader is
cautioned not to rely on these forward- looking statements. These and other
risks are described in detail in Dr. Reddy's Annual Report on Form 10-K for the
year ended December 31, 2019, as filed with the U.S. Securities and Exchange
Commission. All forward-looking statements are based on information currently
available to GRA, and GRA assumes no obligation to update any such
forward-looking statements.
SOURCE: Agility
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