Web28 mag 2024 · The PD-1/PD-L1 inhibitors included pembrolizumab, sintilizumab, nivolizumab, tislelizumab, carrelizumab, teriprizumab, durvalizumab and Atezolizumab. We performed paired analysis in clinical characteristics and treatment modes. Results: There were 155 cases in the RCT group and 150 cases in the RWS group. Web3 apr 2024 · It is planned to include 53 patients with extensive stage small cell lung cancer who have previously received 1-2-line treatment (including one systematic platinum …
Junshi Biological released the first-line Phase III study data of ...
Web7 lug 2024 · Arms, Groups and Cohorts. Experimental: Gemox combined PD1 antibody. Toripalimab (240mg) intravenously, the administration time is 60 (+15) minutes, Q3W is … WebRecently, a study on the first-line treatment of relapsed/metastatic nasopharyngeal carcinoma (JUPITER-02) with teriprizumab combined with chemotherapy was published in the form of cover recommendation in the top 20 international journal Nature Medicine ( IF: 53.440) in the magazine.. This is the first time that Nature Medicine has recommended … gwen mccrae - melody of life
Junshi Bio: Teriplimumab injection is included in the National …
Web2 nov 2024 · The case presented here is that of a male, who enrolled in a phase 2 clinical trial testing the effect of teriprizumab combined with paclitaxel and gemcitabine as a first-line therapy for cholangiocarcinoma. The patient was 71 years of age. The patient developed myocarditis 29 days after the first infusion with teriprizumab. Web6 apr 2024 · Shanghai Junshi Biosciences Co Ltd is a China-based company mainly engaged in innovation-driven biopharmaceutical business. The Company's main businesses are the discovery, clinical research and development of innovative drug s. The Company's main products include teriprizumab injection, Etesevimab, adalimumab injection and … WebRecentemente, Junshi Biotech (1877.HK, 688180.SH) ha annunciato che il farmaco anticorpo monoclonale anti-PD-1 sviluppato dall'azienda teriprizumab per il trattamento del cancro esofageo (CE) è stato approvato dalla Food and Drug Administration ( ( Orphan-drug Designation) concessa dalla FDA.Questa è la quarta designazione di farmaco orfano … gwen mccrae leah mccrae