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临床试验/EUCTR2020-003541-11-EE
EUCTR2020-003541-11-EE进行中(未招募)1 期

A Randomized, Controlled, Open-label Study of the Efficacy, Durability, and Safety of UGN-102 With or Without TURBT in Patients with Low Grade Intermediate Risk Non-Muscle Invasive Bladder Cancer (LG IR-NMIBC) (ATLAS) - A Phase 3 Study of UGN-102 for Low-Grade Intermediate-Risk Non-Muscle Invasive Bladder Cancer(ATLAS)

roGen Pharma Ltd.0 个研究点目标入组 632 人开始时间: 2020年12月28日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
632

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Patient who has newly diagnosed or historic LG NMIBC (Ta) histologically confirmed by cold cup biopsy at screening or within 8 weeks of screening;
  • 2. Is at intermediate risk for progression, defined as having 1 or 2 of the following:
  • a. presence of multiple tumors
  • b. solitary tumor > 3 cm
  • c. recurrence (= 1 occurrence of LG NMIBC within 1 year of the current diagnosis at initial Screening Visit)
  • 3. Negative voiding cytology for high grade (HG) disease within 6 weeks of screening;
  • 4. Has adequate organ and bone marrow function as determined by routine laboratory tests as below:
  • Leukocytes = 3,000/µL (= 3×109/L)
  • Absolute neutrophil count = 1,500/µL (= 1.5×109/L)
  • Platelets = 100,000/µL (= 100×109/L)
  • Hemoglobin = 9.0 g/dL
  • Total bilirubin = 1.5 × upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) (Serum glutamic oxaloacetic transaminase [SGOT])/Alanine aminotransferase (ALT) (Serum glutamic pyruvic transaminase [SGPT]) = 2.5 × ULN
  • Alkaline phosphatase (ALP) = 2.5 × ULN
  • Estimated glomerular filtration rate (eGFR) = 30 mL/min;
  • 5. Has no evidence of active urinary tract infection (UTI);
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 253
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 379

排除标准

  • 1. History of carcinoma in situ (CIS) on preliminary cystoscopy within 5 years of enrollment;
  • 2. Received Bacille de Calmette et Guérin (BCG) treatment for urothelial carcinoma (UC) within previous 1 year;
  • 3. History of HG papillary UC in the past 2 years;
  • 4. History of:
  • a. neurogenic bladder
  • b. active urinary retention
  • c. any other condition that would prohibit normal voiding
  • 5. Past or current muscle invasive (i.e., T2, T3, T4) or metastatic UC or concurrent upper tract urothelial carcinoma (UTUC);
  • 6. Current tumor grading of T1;

研究者

发起方
roGen Pharma Ltd.

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