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Tag: lagevrio

You Searched For "lagevrio"
Merck gets USFDA Priority Review for application for Keytruda plus standard of care as Perioperative treatment for Resectable Locally Advanced Head, Neck Squamous Cell Carcinoma

Merck, Ridgeback Biotherapeutics withdraw COVID pill Molnupiravir application in EU

Ruchika Sharma30 Jun 2023 10:00 AM IST
Merck and Co and partner Ridgeback Biotherapeutics said on Tuesday they had withdrawn their COVID-19 pill application in the European Union,...
Merck gets USFDA Priority Review for application for Keytruda plus standard of care as Perioperative treatment for Resectable Locally Advanced Head, Neck Squamous Cell Carcinoma

Merck beats first-quarter expectations on Keytruda, Gardasil strength

Ruchika Sharma30 April 2023 4:00 PM IST
Bengaluru: Drugmaker Merck & Co Inc on Thursday posted better-than-expected results for the first quarter on the strength of its blockbuster...
EU drug regulator advices against market nod for Merck COVID pill Lagevrio for adults

EU drug regulator advices against market nod for Merck COVID pill Lagevrio for adults

Ruchika Sharma26 Feb 2023 3:45 PM IST
US: The European Union's drug regulator said on Friday its Committee for Medicinal Products for Human Use has advised against market authorisation of...
USFDA removes COVID test requirements for Merck, Pfizer pills

USFDA removes COVID test requirements for Merck, Pfizer pills

Ruchika Sharma2 Feb 2023 12:15 PM IST
The health regulator said individuals with recent known exposure with signs and symptoms may be diagnosed by their healthcare providers with COVID...
Merck, Ridgeback Molnupiravir gets special approval for emergency in Japan

Merck, Ridgeback Molnupiravir gets special approval for emergency in Japan

Ruchika Sharma25 Dec 2021 2:46 PM IST
Kenilworth: Merck, known as MSD outside the United States and Canada, and Ridgeback Biotherapeutics have announced that Japan's Ministry of Health,...
Narrow Vote but Mercks molnupiravir gets USFDA expert panel Yes

Narrow Vote but Merck's molnupiravir gets USFDA expert panel Yes

Ruchika Sharma1 Dec 2021 12:08 PM IST
The vote was 13 for and 10 against authorization

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