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Drug Highest PhaseApproved |
First Approval Ctry. / Loc.CN |
First Approval Date19 Jul 2022 |
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Inactive Indication- |
Drug Highest PhasePhase 2 |
First Approval Ctry. / Loc.- |
First Approval Date- |
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Drug Highest PhasePhase 2 |
First Approval Ctry. / Loc.- |
First Approval Date- |
A Phase IIa Clinical Study of HX301 Alone or in Combination with Temozolomide in Patients with High-Grade Glioma (Grade III and IV)
The study will include a dose-escalation and dose-expansion component to establish the recommended Phase 2 dose (RP2D) for HX301 in combination with Temozolomide and to evaluate the preliminary antitumor activity of HX301.HX301 is an investigational drug that has not yet been approved by the Food and Drug Administration (FDA) or any other regulatory authorities for commercial purposes.
HX301联合替莫唑胺治疗脑胶质母细胞瘤患者的IIa期临床研究
[Translation] Phase IIa clinical study of HX301 combined with temozolomide in the treatment of patients with glioblastoma
评价HX301联合替莫唑胺在治疗脑胶质母细胞瘤患者中的安全性,耐受性及抗肿瘤的疗效。
[Translation] To evaluate the safety, tolerability and anti-tumor efficacy of HX301 combined with temozolomide in the treatment of patients with glioblastoma.
/ Not yet recruitingPhase 1/2 Phase IIa Study of HX009+IN10018 in Patients With Advanced Solid Tumours, Including Biliary Tract Malignancies and Malignant Melanoma, Treated With or Without Standard Chemotherapy
Phase IIa study of HX009+ IN10018 in combination with or without standard chemotherapy in patients with advanced solid tumours including biliary tract malignancies and malignant melanoma
100 Clinical Results associated with Hangzhou Hansi Biological Pharmaceutical Co., Ltd.
0 Patents (Medical) associated with Hangzhou Hansi Biological Pharmaceutical Co., Ltd.
100 Deals associated with Hangzhou Hansi Biological Pharmaceutical Co., Ltd.
100 Translational Medicine associated with Hangzhou Hansi Biological Pharmaceutical Co., Ltd.