Target- |
MechanismImmunostimulants |
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Inactive Indication- |
Drug Highest PhasePhase 1 |
First Approval Ctry. / Loc.- |
First Approval Date- |
/ Not yet recruitingPhase 1IIT A Safety, Tolerability and Efficacy Study of XP-006 Personalized Tumor mRNA Vaccine for Relapsed or Refractory B-Cell Non-Hodgkin's Lymphoma
The main objective of this study is to observe and evaluate the safety and tolerability of the XP-006 personalized tumor mRNA vaccine for the treatment of relapsed or refractory B-cell non-Hodgkin's lymphoma. Secondary objectives focus on evaluating preliminary efficacy through several parameters: XP-006-induced antigen-specific CD4+/CD8+ T cell activation levels, objective remission rate (ORR), complete remission rate (CRR), disease control rate (DCR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS).
/ Not yet recruitingPhase 1IIT A Phase I Clinical Study Evaluating the Safety, Tolerability, and Preliminary Efficacy of XP-001-V2 in Patients with Advanced Solid Tumors
/ RecruitingEarly Phase 1IIT Clinical Study of XP-005 Personalized Vaccine Alone or in Combination With Toripalimab to Prevent the Relapse of Acute Myeloid Leukemia After Consolidation Therapy
The main objective of this study is to observe and evaluate the safety and tolerability of the XP-005 personalized tumor mRNA vaccine, either alone or in combination with toripalimab, for the treatment of acute myeloid leukemia patients who are in remission with minimal residual disease (MRD) positive but cannot undergo allogeneic hematopoietic stem cell transplantation.
100 Clinical Results associated with Shanghai Xinpu Biotechnology Co., Ltd.
0 Patents (Medical) associated with Shanghai Xinpu Biotechnology Co., Ltd.
100 Deals associated with Shanghai Xinpu Biotechnology Co., Ltd.
100 Translational Medicine associated with Shanghai Xinpu Biotechnology Co., Ltd.