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Gilead Sciences Inc

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ISPE announces its manufacturing Facility of the Year Awards winners

28 April 2021 | By Hannah Balfour (European Pharmaceutical Review)

The awardees, including Takeda, Janssen and Gilead, are recognised for their state-of-the-art facility design, construction and operation projects.

Lines of vials labelled 'remdesivir' - idea of scaling up supply of remdesivir

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Gilead to support Indian COVID-19 crisis with donation of remdesivir

27 April 2021 | By Hannah Balfour (European Pharmaceutical Review)

The company will donate 450,000 vials of remdesivir and support its licencing partners in expanding and accelerating the production of the drug.

Capsules and pills of various colours sitting on paper printed with 'HIV/AIDS' repeatedly

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Gilead and Merck to collaborate on long-acting HIV treatments

18 March 2021 | By Hannah Balfour (European Pharmaceutical Review)

The companies have agreed to jointly develop and commercialise long-acting, investigational treatment combinations of lenacapavir and islatravir for HIV.

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Is global COVID-19 expertise accessible enough?

23 July 2020 | By Hannah Balfour (European Pharmaceutical Review)

Does expert knowledge on COVID-19 need to be more accessible across the globe? This article explores this issue and addresses how greater accessibility could help fight the pandemic in emerging countries.

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Inhaled formulation of remdesivir enters clinical trials

13 July 2020 | By Hannah Balfour (European Pharmaceutical Review)

Gilead reveals the novel inhaled formulation of remdesivir entered Phase I trials to establish if it could be used to treat mild to moderate COVID-19.

syrnge filled with liquid in front of the Indian flag

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India approves remdesivir for restricted emergency use in COVID-19 patients

7 July 2020 | By Hannah Balfour (European Pharmaceutical Review)

The Drug Controller General of India (DCGI) approved remdesivir lyophilised powder for emergency use in patients hospitalised with severe COVID-19.

coronavirus particles in yellow on a blue background

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Developers request revocation of remdesivir’s ODD for COVID-19

26 March 2020 | By Hannah Balfour (European Pharmaceutical Review)

Gilead Sciences say they are confident they can maintain an expedited regulatory review timeline for remdesivir as a treatment for COVID-19 without Orphan Drug Designation (ODD).

puzzle pieces surrounded by city skyscrapers coming together

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Gilead set to acquire Forty Seven for $4.9bn later in 2020

5 March 2020 | By Hannah Balfour (European Pharmaceutical Review)

Gilead's acquisition of Forty Seven was unanimously approved by both companies' Boards of Directors, for $95.50 per share.

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Decision upheld in Merck hepatitis C drugs patent case

5 November 2019 | By Rachael Harper (European Pharmaceutical Review)

A US appeals court has upheld a ruling that threw out a $2.54 billion jury verdict Merck won against Gilead over hepatitis C treatments.

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Combination therapy suppresses HIV-like virus in primates

7 March 2018 | By Dr Zara Kassam (European Pharmaceutical Review)

Broadly neutralising antibody treatment may target viral reservoir in monkeys...

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