6
项与 卡介苗(安徽智飞龙科马生物) 相关的临床试验A Randomized, Double-blind, Active-controlled, Multicenter Phase III Clinical Trial Evaluating the Efficacy and Safety of Therapeutic BCG for the Prevention of Postoperative Recurrence of Non-muscle-invasive Bladder Cancer in People Aged 18 Years and Older
Research topic: A randomized, double-blind, active-controlled, multicenter phase III clinical trial evaluating the efficacy and safety of therapeutic BCG for the prevention of postoperative recurrence of non-muscle-invasive bladder cancer in people aged 18 years and older.
The name of the drug: Bacillus Calmette-Guérin for treatment(BCG). Clinical indications: It is used for the treatment of bladder carcinoma in situ and the prevention of recurrence, and for the prevention of recurrence of bladder papilloma after transurethral resection in Ta or T1 stage. This product is not used for papillomas beyond the T1 stage.
Study population: Patients aged 18 years and above with intermediate- and high-risk non-muscle-invasive bladder cancer (NMIBC) who have undergone transurethral bladder tumor resection.
Objectives: Primary Objectives: To assess the effectiveness of BCG for therapeutic use in the adjuvant treatment of intermediate- and high-risk NMIBC after transurethral resection of bladder tumors. Secondary Purpose: To assess the safety of the therapeutic BCG vaccine in the adjuvant treatment of intermediate- and high-risk NMIBC after transurethral resection of bladder tumors. Other purposes: To assess the pharmacodynamic (PD) profile of BCG for therapeutic use in the adjuvant treatment of intermediate- and high-risk NMIBC after transurethral resection of bladder tumors.
Study design: This study adopts a randomized, double-blind, active-controlled, multi-center trial design, including three phases: screening period, treatment period and follow-up period. In this study, 438 subjects will be randomly assigned to the experimental group and the control group in a 1:1 ratio, with 219 patients in both the experimental group and the control group, and stratified according to the baseline risk level (high-risk/intermediate-risk) and whether or not to perform urine PD sample collection (yes/no).
Phase I Clinical Trial to Evaluate the Safety and Tolerability of BCG for Therapeutic Use in Preventing Postoperative Recurrence of Non-muscular Invasive Bladder Cancer in People Aged 18 and Over
This clinical study adopted a single-arm, open, single-centertrial design. The purpose of this study was to evaluate the safety and tolerability, PK characteristics, shedding and immune response characteristics of BCG for therapeutic use developed by Anhui Zhifei Longcom Biologic Pharmacy Co., Ltd. in patients aged 18 and over after transethral resection of non-muscular invasive bladder cancer.
评价治疗用卡介苗用于预防18周岁及以上人群非肌层浸润性膀胱癌术后复发的安全性和耐受性的I期临床试验
主要目的:评价治疗用卡介苗用于预防18周岁及以上人群非肌层浸润性膀胱癌术后复发的安全性和耐受性,为后续Ⅲ期临床试验的开展提供数据支持。次要目的:(1)评价评价治疗用卡介苗在18周岁及以上非肌层浸润性膀胱癌经尿道切除术后患者中的药代动力学(PK)特征;(2)考察治疗用卡介苗在18周岁及以上非肌层浸润性膀胱癌经尿道切除术后患者体内的脱落情况和免疫应答特征。
100 项与 卡介苗(安徽智飞龙科马生物) 相关的临床结果
100 项与 卡介苗(安徽智飞龙科马生物) 相关的转化医学
100 项与 卡介苗(安徽智飞龙科马生物) 相关的专利(医药)
100 项与 卡介苗(安徽智飞龙科马生物) 相关的药物交易