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Roche Holding plans to sell 800-employee drug manufacturing plant in Vacaville

The company said it is seeking a buyer that will continue to use the plant as an operating facility.

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Roche gets USFDA priority review for Actemra to treat Covid-19

Basel: Roche today announced that the U.S. Food and Drug Administration (USFDA) has accepted the company's supplemental Biologics License Application (sBLA) and has granted Priority Review for...

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Medicii britanici dau undă verde unui cocktail de anticorpi împotriva coronavirusului

Agenţia britanică pentru medicamente a aprobat vineri un cocktail de anticorpi produs de Regeneron şi Roche în scopul prevenirii şi tratării...

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唐獎得主開發藥物安挺樂 FDA緊急授權治療新冠病人 - 生活

2020年唐獎生技醫藥得主、日本大阪大學教授岸本忠三及其團隊與國際藥廠合作研發的IL-6受體抗體藥物,24日通過美國食藥署(FDA)通過緊急授權,將成為美國藥廠Genetech藥廠開發的安挺樂Actemra藥物,用以治療新冠病人。

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Govt should issue compulsory licences to boost covid drugs production: IDMA


Govt should issue compulsory licences to boost covid drugs production: IDMA
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(AFP)
The Indian Drug Manufacturers’ Association (IDMA) on Wednesday urged the government to use provisions of the World Trade Organization (WTO) to issue compulsory licences to pharma firms to make drugs such as remdesivir that are used in the treatment of covid
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The Indian Drug Manufacturers’ Association (IDMA) on Wednesday urged the government to use provisions of the World Trade Organization (WTO) to issue compulsory licences to pharma firms to make drugs such as remdesivir that are used in the treatment of covid.
“WTO has also provided the provision of compulsory licensing just for tackling such an eventuality. Our government should not feel shy in invoking this in the interest of humanity and our citizens," IDMA said in a position paper on patent waivers.

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Roche says adding Actemra to Gilead's remdesivir didn't cut COVID patient hospital stays

Roche says adding Actemra to Gilead's remdesivir didn't cut COVID patient hospital stays
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Roche's arthritis drug Actemra scores FDA nod in rare autoimmune disease after partial clinical win


Mar 5, 2021 11:20am
Roche's Actemra has become the first biologic that the FDA approved for patients with systemic sclerosis-associated interstitial lung disease. (Roche/Genentech)
Missed the primary endpoint of a clinical trial? No problem. We’ll pick the study apart and approve your drug based on a post-hoc subgroup analysis.
That’s what the FDA did in granting Roche’s Actemra a go-ahead in patients with interstitial lung disease (ILD) associated with the rare autoimmune disease systemic sclerosis (SSc).
The approval makes Actemra the first biologic drug cleared by the FDA to slow the decline in pulmonary function in patients with SSc-ILD, Roche’s Genentech said Thursday.

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The Latest: Florida urges more vaccine for its many seniors

COLOMBO, Sri Lanka — Sri Lanka is welcoming tourists again after keeping the doors...

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The Latest: Britain hits another record daily virus deaths

COLOMBO, Sri Lanka — Sri Lanka is welcoming tourists again after keeping the doors...

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