CStone's sugemalimab to face stiff competition in NSCLC segment in China

21 June 2022
cstone_logo

The National Medical Products Administration (NMPA) of China has recently approved Chinese biotech firm CStone Pharmaceuticals’ (HKEX: 2616) sugemalimab (trade name Cejemly) to treat patients with stage III non-small cell lung cancer (NSCLC), whose disease has not progressed following concurrent or sequential or platinum-based chemoradiotherapy.

Against this backdrop, sugemalimab will still face stiff competition in China, observes data and analytics company GlobalData.

Notably, the Chinese Society of Clinical Oncology 2022 guideline has already recommended sugemalimab: level 1 for stage IV NSCLC and level 3 for stage III NSCLC.

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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

Today's issue

Company Spotlight





More Features in Biotechnology