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Clinical Trials associated with Targeting Survivin DC Cells (Tricision) / Not yet recruitingPhase 1 Phase I Clinical Study of Targeted Survivin DC Cell Injection for the Treatment of Newly Diagnosed Primary Glioblastoma Multiforme (GBM)
Primary Objective: To evaluate the safety and tolerability of targeted Survivin DC cell injection for postoperative treatment of newly diagnosed primary glioblastoma multiforme. Secondary Objectives: Utilize progression-free survival (PFS) and overall survival (OS) to preliminarily assess the effectiveness of targeted Survivin DC cell injection for postoperative treatment of newly diagnosed primary glioblastoma multiforme in China. Evaluate the immunological effects of targeted Survivin DC cell injection. Explore the impact of targeted Survivin DC cell injection on human DC cell activity and in vivo processes.
Patients will undergo a combined treatment of radiotherapy and temozolomide (TMZ) for a duration of 6 weeks, with concurrent chemotherapy. After completing this phase, there will be a 4-week interval (28 days) before entering multiple cycles of adjuvant TMZ chemotherapy. Each cycle will last 28 days, involving daily oral administration of temozolomide at a dose of 150-200mg/m2 for 5 consecutive days, followed by a 23-day drug-free period. This entire cycle will be repeated every 28 days. Nine days after completing the standard 6-week concurrent chemoradiotherapy, targeted Survivin DC cell injections will be administered. The injections will be given on days 0, 14, and 28. The administration will involve both intradermal (ID) and intravenous (IV) routes. Four hours before the administration, the injection sites will be pre-treated with lidocaine cream. The injection procedures will be conducted sequentially, starting with ID injection. After completing the ID injection, a 30-minute observation will be conducted. If no adverse reactions are observed, IV infusion will be initiated. Both IV infusion and ID injection will be performed on the same side. Intradermal Injection: Draw 1ml of cell suspension with a 1ml syringe, and the remaining cell product will be stored at 2-8℃. Administer the drug immediately after preparation. Intravenous Infusion: Before administration, infuse 20ml of normal saline through IV.Extract 25ml of normal saline, dilute the remaining cell product (5ml), and administer it through IV infusion. Control the room temperature during infusion and complete it within 30 minutes. After administration, inject 50ml of normal saline into the cell bag to ensure all cell products are returned to the patient's body.
/ Not yet recruitingPhase 1IIT Phase I clinical Study of Targeted Survivin DC Cell Injection for the Treatment of Newly Diagnosed Primary Glioblastoma Multiforme (GBM)
/ Not yet recruitingPhase 2 评价靶向Survivin DC细胞注射液治疗新诊断的脑胶质母细胞瘤的有效性和安全性的II期临床研究
[Translation] A Phase II clinical trial evaluating the efficacy and safety of targeted Survivin DC cell injection for the treatment of newly diagnosed glioblastoma.
本研究的总体目标是初步评估靶向Survivin DC细胞注射液用于新诊断的脑胶质母细胞瘤的术后治疗的有效性和安全性。
IIa期目的:
1-通过DLT评估靶向Survivin DC细胞注射液的安全性;
2-确定最大耐受剂量(MTD),评估推荐的Ⅱb期剂量(RP2D);
3-探索靶向Survivin DC细胞注射液人体DC细胞活性和体内过程。
Ⅱb期目的: 1-采用PFS、OS,初步评估靶向Survivin DC细胞注射液用于新诊断的脑胶质母细胞瘤的术后治疗的有效性;
2-评估靶向Survivin DC细胞注射液的安全性;
3-评估靶向Survivin DC细胞注射液的免疫效应。
[Translation] The overall objective of this study is to preliminarily evaluate the efficacy and safety of targeted Survivin DC cell injection for the postoperative treatment of newly diagnosed glioblastoma.
Phase IIa Objectives:
1- Assess the safety of targeted Survivin DC cell injection using dose-dependent immunotherapy (DLT);
2- Determine the maximum tolerated dose (MTD) and evaluate the recommended phase IIb dose (RP2D);
3- Explore the human DC cell activity and in vivo processes of targeted Survivin DC cell injection.
Phase IIb Objectives:
1- Preliminarily evaluate the efficacy of targeted Survivin DC cell injection for the postoperative treatment of newly diagnosed glioblastoma using progression-free survival (PFS) and overall survival (OS);
2- Assess the safety of targeted Survivin DC cell injection;
3- Assess the immune effects of targeted Survivin DC cell injection.
100 Clinical Results associated with Targeting Survivin DC Cells (Tricision)
100 Translational Medicine associated with Targeting Survivin DC Cells (Tricision)
100 Patents (Medical) associated with Targeting Survivin DC Cells (Tricision)
100 Deals associated with Targeting Survivin DC Cells (Tricision)