Karyopharm Therapeutics (Nasdaq: KPTI) and privately-held Italian drugmaker Menarini Group today announced that the UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) has granted full Marketing Authorization for Nexpovio (selinexor) in combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.
With this approval extending Nexpovio’s indication in Great Britain, the conditional marketing authorization is now converted to full approval. Stemline Therapeutics, a wholly owned subsidiary of Menarini, will be responsible for all commercialization activities in the UK.
The drug is also approved and marketed in the USA by Karyopharm under the trade name Xpovio. It was also cleared for marketing in Europe in July last year.
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