No Data
No Data
Express News | Shanghai Junshi Biosciences - Approval of Supplemental New Drug Application for Toripalimab as First-Line Treatment of Es-Sclc by Nmpa
Junshi Biosciences (688180.SH): There are currently no COVID-19 vaccine products in the development pipeline.
Junshi Bio (688180.SH) stated on the investor interaction platform on June 12 that there is currently no vaccine product against COVID-19 in the company's research and development pipeline.
Junshi Bio (688180.SH): The new indication for the use of Toripalimab monotherapy in first-line treatment for extensive-stage small cell lung cancer has been approved for market application.
On June 12th, Gelunhui reported that Junshi Bio (688180.SH) has received a 'Pharmaceutical Registration Certificate' approved and issued by the National Medical Products Administration for Toripalimab (Commodity Name: Tuoyi, Product Code: JS001), which is used in combination with Icotinib and Platinum-based drugs for the first-line treatment of extensive-stage small cell lung cancer (ES-SCLC) as a new indication. Due to the commercialization of medicine that can be affected by certain uncertainties after obtaining market approval.
Junshi Bio Achieves Primary Endpoints in Phase 3 Trial of Liver Cancer Treatment
Shanghai Junshi Biosciences (SHA:688180, HKG:1877) achieved the primary endpoints of a phase 3 trial for its toripalimab advanced liver cancer treatment, according to a Wednesday filing with the Shang
Shanghai Junshi Biosciences Cancer Drug Shows Positive Phase III Trial Results
Shanghai Junshi Biosciences (HKG:1877) announced positive results from a Phase III clinical trial testing its drug toripalimab in combination with bevacizumab for advanced hepatocellular carcinoma (HC
Express News | Junshi Biosciences Announces Phase 3 Study of Toripalimab Combined With Bevacizumab for the First-Line Treatment of Advanced Hepatocellular Carcinoma Meets Primary Endpoint
No Data