Japanese drugmaker Chugai Pharmaceutical (TYO: 4519) said on Friday that it has launched the ALK inhibitor Alecensa (alectinib hydrochloride) for the indication of ALK fusion gene positive unresectable, recurrent/advanced non-small cell lung cancer (NSCLC).
Alecensa received a manufacturing and marketing approval in Japan on July 4, making this the first country to clear the drug, and was listed on the National Health Insurance (NHI) reimbursement price list on September 2, 2014.
Alecensa is a highly selective ALK inhibitor created at Chugai Kamakura Research Laboratories. The drugmaker says that Alecensa exemplifies the personalized health care (PHC) strategy promoted by Chugai and its majority owner, Switzerland’s Roche (ROG: SIX), which has in-licensed the drug for territories including Europe and the USA.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze