
Chinese regulator the National Medical Products Administration (NMPA) has approved Tyvyt (sintilimab) for the treatment of patients with classical Hodgkin's lymphoma (cHL) that has relapsed or refractory (r/r) after two or more lines of systemic chemotherapy (r/r cHL).
The approval of Tyvyt highlights the emergence of China in the field of immuno-oncology, said the product’s co-developers, Chinese biotech firm Innovent Biologics (HKEX: 01801) and US pharma major Eli Lilly (NYSE: LLY). Innovent’s shares gained 1.68% to HK$21.20 on the news.
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
| Headless Content Management with Blaze