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Lilly’s neutralizing antibody bamlanivimab receives FDA emergency use authorization for the treatment of recently diagnosed COVID-19

The U.S. FDA granted Emergency Use Authorization for Eli Lilly and Company's investigational neutralizing antibody bamlanivimab 700 mg. Bamlanivimab is authorized for the treatment...

Transcenta and Merck Announce a Strategic Collaboration at CIIE to Advance Continuous Biomanufacturing

Transcenta, a global biotherapeutics company with fully-integrated capabilities in discovery, development and manufacturing of antibody-based therapeutics, and Merck, a leading science and technology company,...

Australia begins production of Oxford Covid-19 vaccine, plans to manufacture 30 million doses

A Covid-19 vaccine co-developed by pharmaceutical company AstraZeneca and the University of Oxford is seen as one of the most promising of all the...

Brazil Suspends Trials Of Chinese Covid-19 Vaccine Due To Adverse Incident

Brazilโ€™s health regulator halted clinical trials of the potential coronavirus vaccine CoronaVac, citing an adverse, serious event, according to a statement it posted to...

Cancer Treatment Can Be Cloned For COVID-19

As per the recent international study by the scientists from Italy & Australia, Beta-blockers have it in them to be a potential treatment for...

A New Senate & its implications on The Pharmaceutical Sector?

The US elections make big news whenever they occur. The fact that who comes to power has a phenomenal effect on all industries, big...

AstraZeneca Says Calquence Approved In The EU For CLL

AstraZenecaโ€™s Calquence (acalabrutinib), a next-generation selective Brutonโ€™s tyrosine kinase (BTK) inhibitor, has been approved in the European Union (EU) for the treatment of adult...

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