Takeda (TYO: 4502) announced on Wednesday that Ninlaro (ixazomib) achieved its primary endpoint in the Phase III TOURMALINE-MM3 trial oriented toward multiple myeloma treatment.
Ninlaro's effectiveness exceeded placebo in the treatment of adult patients diagnosed with multiple myeloma who responded to high-dose therapy and autologous stem cell transplant.
The Japanese pharma major has indicated its intention to share this data with global regulatory agencies. Ninlaro is not currently approved as a maintenance therapy anywhere in the world.
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