Celltrion said that the Brazilian health authorities on Aug. 11 approved Regkirona for high-risk adult patients with mild and moderate symptoms. The company added that the approval was based on the effective test results from its phase 1, 2 and 3 clinical trials as well as preclinical data on Delta and Gamma variants.
The number of confirmed cases in Brazil has been on the rise lately due to the fast spread of the delta variant. More than 35,000 patients were confirmed with COVID-19 in the country on Aug. 11 alone.
“Our company will accelerate the delivery of Regkirona to Brazil to help the patients to recover faster,” said a Celltrion official.
Celltrion is currently having a preliminary discussion with the Food and Drug Administration (FDA) in the US regarding the regulatory filing, while the European Medicines Agency (EMA) is conducting a review on Regkirona.
Prior to its official approval, the EMA in March granted Regkirona a recommendation to use by the EU member states. The recommendation allows European countries to use the treatment prior to the official outcome of the health regulator’s review.
Moreover, Pakistan’s state-owned company Wah Industries Ltd., purchased 100,000 vials of Regkirona in March to treat the country’s soldiers and the general public confirmed with COVID-19. Celltrion said the contracted amount of 100,000 vials is enough to treat 30,000 patients.
In South Korea, Celltrion has asked the Ministry of Food and Drug Safety (MFDS) to widen the scope of Regkirona’s use to include minors over the age of 12 as well as adults with mild and moderate symptoms. The Korean health regulator currently allows Regkirona to be used only on high-risk patients or those older than 60.
Write to Jae-young Han at jyhan@hankyung.com Daniel Cho edited this article.
We use cookies to provide the best user experience. By continuing to browse this website, you will be considered to accept cookies. Please review our Privacy Policy to learn our cookie policy.