Price not so NICE for routine use of Opdivo in melanoma

Last updated: Nov. 5, 2020

The latest global regulatory news, changes and updates affecting biopharma, including: Price not so NICE for routine use of Opdivo in melanoma; MHRA updates EAMS guidance; HHS plans retrospective regulatory review; USPTO sees spike in AI-related patent applications.

BioWorld Regulatory

Accuracy, utility of COVID-19 lateral flow tests questioned in the U.K.

BioWorld MedTech

LONDON – A huge row has broken out in the U.K. about the accuracy and utility of COVID-19 lateral flow tests (LFT) in screening asymptomatic people, as a pilot...

Israel continues to shine as hub of med-tech innovation

BioWorld MedTech

In recent years, Israel has proven to be a hot spot for med-tech innovation. The country boasts more than 1,500 companies in the health care and life sciences...

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BioWorld briefs for Jan. 20.

Sarepta DMD phase II hangs in ‘balance’ as disparity in North Star leads astray

BioWorld

Sarepta Therapeutics Inc.’s miss on a key phase II ambulatory endpoint in its Duchenne muscular dystrophy (DMD) trial may have been caused by a dramatic disparity...

Sinovac’s COVID-19 vaccine more than 78% effective in Brazil trials

BioWorld

CAJICA, Colombia – Brazil's Butantan Institute and the government of the state of Sao Paulo released efficacy results on Jan. 7 for Coronavac, developed by...