Hetero Enters Into a Licensing Agreement With Gilead Sciences, Inc. for the Manufacturing and Distribution of "Remdesivir"
PR84025
Hetero Enters Into a Licensing Agreement With Gilead Sciences, Inc. for the Manufacturing and Distribution of "Remdesivir" in 127 Countries, Including India, for COVID-19
HYDERABAD, India, May 14, 2020 /PRNewswire=KYODO JBN/ --
Hetero, one of India's leading generic pharmaceutical companies and the world's
largest producer of anti-retroviral drugs, announced today that it has entered
into a licensing agreement with Gilead Sciences, Inc. for the manufacturing and
distribution of "Remdesivir" for the treatment of Covid-19. Under this
licensing deal, Hetero will be supplying Remdesivir in 127 countries, including
India, subject to regulatory approvals in respective countries.
Dr. B. Partha Saradhi Reddy, Chairman, Hetero Group of Companies, commented:
"Hetero is pleased to partner with Gilead to enable access for this important
drug to India and other developing countries at this crucial time. This
agreement also illustrates the significance of global collaboration and the
need for coming together to fight the health crises impacting humanity. Hetero
has developed this product in India and has already been working with the
government, ICMR, and DCGI for necessary studies and approvals to bring this
product to treat COVID-19 patients in India."
Remdesivir will be manufactured in our formulation facility in Hyderabad,
India, which has been approved by stringent global regulatory authorities such
as USFDA and EU, among others. Hetero has developed the fully vertically
integrated supply chain for this product complementing the "Make in India"
campaign as defined by our Hon'ble Prime Minister.
Important Information about Remdesivir
U.S. Food and Drug Administration (FDA) has granted emergency use authorization
(EUA) for the investigational antiviral Remdesivir to treat COVID-19.
Remdesivir is authorized for the treatment of hospitalized patients with severe
COVID-19 disease. The optimal duration of treatment is still being studied in
ongoing clinical trials. Under the EUA, both 5-day and 10-day treatment
durations are suggested, based on the severity of disease. The authorization is
temporary and does not take the place of the formal new drug application
submission, review and approval process. The EUA allows for the distribution
and emergency use of Remdesivir only for the treatment of COVID-19; Remdesivir
remains an investigational drug and is not approved anywhere globally including
US and India.
About Hetero
Hetero is one of India's leading generic pharmaceutical companies and the
world's largest producer of anti-retroviral drugs. With 25 years of expertise
in the pharmaceutical industry, Hetero's strategic business areas spread across
APIs, generics, biosimilars, custom pharmaceutical services and branded
generics.
Hetero has 36 state-of-the-art manufacturing facilities, 300 plus products in
its portfolio and has a strong global presence in over 126 countries. For more
information on Hetero, please visit www.heteroworld.com.
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Media Contact:
Jeyasingh Balakrishnan
Head – Corporate Communications
Hetero Labs Limited
Mobile: (+91) 9989626541, (+91) 9833836185
Source: Hetero
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