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Gilead Sciences Inc

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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.

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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).

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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.

news

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.

news

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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Recommended

Gilead Sciences Inc

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

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

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

Decision upheld in Merck hepatitis C drugs patent case

Combination therapy suppresses HIV-like virus in primates