With the world waiting, Roche socks $459M into COVID-19 antibody test production

Roche
Roche received the FDA's emergency use nod for its COVID-19 antibody test late last week. (Roche)

Roche scored a major win with the FDA's backing for its COVID-19 antibody tests last week in a field marked by products of questionable quality. Now, to cover its booming production goals, Roche plans to infuse nearly half-a-billion dollars into its German manufacturing facility. 

Roche will plow $459 million into its manufacturing facility in Penzberg, Germany, to boost production of the antibody test that won an emergency use authorization from the FDA last week, Reuters reported

At a German Ethics Council meeting Monday, officials said the government had signed a deal with Roche to secure 3 million diagnostic tests in May and an additional 5 million each following month. Eventually, Roche will aim to produce nearly 100 million tests per month by the end of 2020, according to Reuters. 

Roche is reportedly also working on a four-year plan to develop a brand-new research and diagnostic center. 

After the FDA approval Friday, Roche said it is prepared to produce "high double-digit millions" of the tests in May with the intent to continue ramping up production. 

RELATED: COVID-19 antibody testing 'a disaster,' says Roche CEO, as diagnostics sales rise

Roche began testing its antibody diagnostic, which runs on its high-throughput Elecsys assay platform and cobas line of analyzers, in mid-April.

During a first-quarter earnings call with analysts late last month, Roche CEO Severin Schwan blasted the current state of COVID-19 serology tests, calling many of the diagnostics "amateur."

“These tests are not worth anything, or have very little use,” Schwan said at the time. “Some of these companies, I tell you, this is ethically very questionable to get out with this stuff." 

RELATED: FDA grants Roche coronavirus test emergency green light within 24 hours

Roche has not only scored an emergency use nod for antibody tests but also for a fully automated molecular test for active COVID-19 patients. 

The FDA authorized Roche's diagnostic test in mid-March, just 24 hours after receiving the application. Previously, the FDA had only allowed specific, certified laboratories to use their preapproved and validated diagnostics in identifying COVID-19 patients.

Now, this latest Emergency Use Authorization enables clinicians to run the Roche test on the company’s cobas 6800/8800 molecular testing systems, widely available at hospitals and labs throughout the country. It is also available in European countries accepting the CE mark.

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