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US officials authorize emergency use of antibody-drug Actemra from Roche

U.S. health officials have granted emergency use for another antibody-drug to help hospitalised patients with the most dangerous cases of COVID-19.
The Food and Drug Administration said late Thursday it authorized the drug Actemra from Roche for hospitalised patients who are already receiving steroid drugs, oxygen and other measures to fight COVID-19.
When added to those treatments, studies showed Roche s drug reduced the risk of death and cut hospitalisation time.
Actemra does not target the coronavirus directly but instead helps reduce inflammation, a driver of the disease. It is already approved for rheumatoid arthritis and several other diseases.
The FDA has cleared several antibody drugs for COVID-19 but there has been low demand because of the hurdles of delivering them via IV at hospitals or clinics. ....

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FDA Gives Third COVID-19 Antibody Drug Emergency Use Approval

Another COVID-19 antibody-drug has been given emergency use approval by the U.S. Food and Drug Administration. The said drug was developed by GlaxoSmithKline and Vir Biotechnology. ....

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Global sales of Celltrion's COVID-19 antibody-drug Regkirona begin

Global sales of Celltrion s COVID-19 antibody-drug Regkirona begin
ANI |
Updated: May 12, 2021 07:56 IST
Seoul [South Korea], May 12 (ANI/Global Economic): Worldwide sales of Regkirona (active ingredient: regdanvimab), a COVID-19 antibody drug developed by South Korean biopharmaceutical company Celltrion Inc, has begun.
Celltrion Healthcare Co Ltd, the marketing arm of Celltrion, announced on Monday that it has signed a contract with a Pakistani state-owned company to export 100,000 vials of Regkirona. The total supply is a sufficient amount to administer to about 30,000 people.
The contractee is a subsidiary of Pakistan Ordnance Factories (POF), the largest defense contractor under Pakistan s Ministry of National Defense. The plan is to administer the first batch to Pakistani soldiers and the public. ....

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