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Inactive Indication- |
Drug Highest PhaseApproved |
First Approval Ctry. / Loc. |
First Approval Date08 May 2017 |
一项观察性双向队列研究评估达妥昔单抗β和常规治疗用于高危神经母细胞瘤患者维持治疗长期有效性和安全性
[Translation] An observational bidirectional cohort study evaluating the long-term efficacy and safety of datuximab beta versus conventional therapy for maintenance treatment of patients with high-risk neuroblastoma
本研究将收集达妥昔单抗β药品上市后在真实医疗环境中治疗高危神经母细胞瘤患者的数据,评估在维持治疗阶段使用达妥昔单抗β与常规治疗方案的有效性和安全性。研究结果将桥接境外临床研究数据,用于支持达妥昔单抗β获得最终完全的批准。
[Translation] This study will collect data on the treatment of high-risk neuroblastoma patients in real medical settings after the launch of datuximab beta, and evaluate the effectiveness and safety of using datuximab beta in the maintenance treatment phase compared with conventional treatment regimens. The results of the study will bridge the overseas clinical research data to support the final full approval of datuximab beta.
100 Clinical Results associated with Millmount Healthcare Ltd.
0 Patents (Medical) associated with Millmount Healthcare Ltd.
100 Deals associated with Millmount Healthcare Ltd.
100 Translational Medicine associated with Millmount Healthcare Ltd.