Regeneron asks FDA for emergency clearance for COVID-19 therapy

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print

Regeneron has submitted a request to FDA for Emergency Use Authorization approval for the

REGN-COV2 investigational antibody combination for COVID-19.

REGN-COV2 is a combination of two monoclonal antibodies (REGN10933 and REGN10987) and was designed specifically to block infectivity of SARS-CoV-2. The agent was recently used to treat President Donald Trump.

If an EUA is granted, the government has committed to making these doses available at no cost, and would be responsible for their distribution.

At this time, there are doses available for approximately 50,000 patients. Regeneron said it expects to have doses available for 300,000 patients in total within the next few months.

Table of Contents

YOU MAY BE INTERESTED IN

Those of us who have devoted our careers to treating recalcitrant cancers know the heartbreak of walking alongside an individual facing an advanced diagnosis. We not only shoulder the clinical responsibility, but also the emotional weight that accompanies every step of that journey as each patient’s story becomes connected to our own.
If you believe in the miraculous healing power of ivermectin, hydroxychloroquine, and the harm from vaccination for HPV and COVID-19, you’ve got a powerful friend in Sen. Ron Johnson (R-WI), chair of the Permanent Subcommittee on Investigations of the Senate Committee on Homeland Security and Governmental Affairs.
In a poignant keynote punctuated with anecdotes about grief, American Society of Clinical Oncology’s immediate past president Eric Small emphasized that the annual conference is not just about scientific discovery, but about a responsibility to translate discoveries into better outcomes for cancer patients globally. 

Never miss an issue!

Get alerts for our award-winning coverage in your inbox.

Login