CStone’s sugemalimab recommended for metastatic NSCLC

The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended the approval of CStone’s sugemalimab, an anti-PD-L1 monoclonal antibody (mAb), for first-line treatment of metastatic non-small cell lung cancer (NSCLC).  

CStone’s sugemalimab has been recommended in combination with chemotherapy as a first-line treatment for NSCLC.

The endorsement could mark the first anti-PD-L1 monoclonal antibody approved for both squamous and non-squamous NSCLC, irrespective of PD-L1 expression, in Europe.

The CHMP’s positive opinion is based on the GEMSTONE-302 study, a multi-centre, randomised, double-blind, Phase 3 clinical trial showing significant improvements in progression-free survival (PFS) and overall survival (OS) when sugemalimab is combined with chemotherapy in previously untreated stage IV NSCLC patients.

CStone CEO, executive director and research and development president Dr Jason Yang stated: “The positive opinion from EMA CHMP normally indicates an upcoming approval for market authorisation by the European Commission, marking a significant milestone not only for sugemalimab but also for CStone and the entire pharmaceutical industry in China.

“The CHMP recommendation brings us closer to delivering this innovative treatment to European patients with lung cancer, and it also highlights a major milestone in CStone’s global strategy.”

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Your download email will arrive shortly

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData

Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

CStone has already secured approval for sugemalimab in China for five cancer indications.

In China, the National Medical Products Administration (NMPA) has approved sugemalimab for stage III and IV NSCLC, extranodal NK/T-cell lymphoma, oesophageal squamous cell carcinoma and gastric cancer. 

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) is undertaking a marketing authorisation application review for sugemalimab for metastatic NSCLC.

CStone is in discussions with the EMA, the UK Medicines and Healthcare products Regulatory Agency, and the US Food and Drug Administration for additional indications.

It is looking at development and commercialisation partnerships in countries and regions worldwide.