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

US health officials have granted emergency use for another antibody-drug to help hospitalised patients with the most dangerous cases of Covid-19.

Drugmaker Roche to buy US' cancer medicine specialist Ignyta for $1.7 bn
Swiss Drugmaker Roche. Photo: Reuters
AP Washington
1 min read Last Updated : Jun 26 2021 | 9:27 AM IST

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.

Health officials have emphasised the need to develop more pill-based drugs for COVID-19.

(Only the headline and picture of this report may have been reworked by the Business Standard staff; the rest of the content is auto-generated from a syndicated feed.)

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Topics :CoronavirusRocheUS drug approvals

First Published: Jun 26 2021 | 9:27 AM IST

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