BUSINESS

Daiichi Sankyo’s HER3 ADC Gets Breakthrough Therapy Tag in US

December 27, 2021
Daiichi Sankyo said on December 23 that its HER3 directed antibody drug conjugate (ADC) patritumab deruxtecan obtained Breakthrough Therapy designation from the US FDA for the treatment of certain patients with EGFR-mutated non-small cell lung cancer (NSCLC).The status was granted…

To read the full story

Related Article

BUSINESS

By Philip Carrigan

As the year 2022 draws to a close, what are managers thinking at the world’s leading pharmaceutical companies and medical device companies? We surveyed 86 managers at these companies to find out what’s on their minds.For many managers, a common…

By Yoshinori Sagehashi

Debates on the planned FY2023 off-year drug price revision are now entering the final stretch. Healthcare providers and payers have made their conflicting positions clear on the scope of products to be covered by the re-pricing, while the pharma industry…

A Japanese reimbursement policy panel on November 16 saw a continued scuffle between members representing healthcare providers and payers over…

Deloitte Tohmatsu Consulting proposed three drug pricing schemes designed to trigger the consolidation of generic makers on October 27, offering…

Authorized generic (AG) strategies taken by innovative drug makers might help soften the impact of generic competition in their businesses but such tactics might also accelerate the application of “G1”/“G2” price cuts for their off-patent brand-name medicines, a Jiho tally…

Japan’s health ministry announced new NHI prices to be applied in April under the FY2022 drug price revision in the official gazette on March 4, with the earlier application of so-called “G1” price cuts to be implemented for the first…