跳至主要内容
临床试验/EUCTR2013-005455-32-Outside-EU/EEA
EUCTR2013-005455-32-Outside-EU/EEA进行中(未招募)不适用

Open-Label, Multicenter, Multiple Oral Dose Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety of Canagliflozin in Older Children and Adolescents =10 to <18 years of age with Type 2 Diabetes Mellitus and Currently on a Stable Dose of Metformin.

Janssen-Cilag International NV0 个研究点目标入组 16 人开始时间: 2014年1月10日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
16

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

  • - Diagnosed with Type 2 Diabetes Mellitus
  • - Be on a stable regimen of metformin immediate release (IR) monotherapy of at least 1,000 mg/day for at least 8 weeks before screening
  • - Able to swallow whole tablets
  • - Absence of pancreatic autoimmunity
  • - Participants and their caregivers must agree to perform the fasting fingerstick glucose self-monitoring during the study
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 16
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - History of Type 1 diabetes mellitus
  • - History of maturity onset diabetes of the young (MODY) and any secondary form of diabetes
  • - Current clinically significant medical illness e.g., significant pulmonary disease, renal or hepatic insufficiency, uncontrolled thyroid disease
  • - Systolic or diastolic blood pressure outside the range considered normal for the participant sex, age and height
  • - For females, participants will be excluded if pregnant

研究者

相似试验

已完成
不适用
An open-label, multiple oral dose study to investigate the plasma and CSF pharmacokinetics of CAD-1883 in healthy volunteers
NL-OMON47994Cadent Therapeutics Inc.8
已完成
1 期
An Ascending Multiple Dose Study of SEP-363856 in Japanese Subjects with Schizophreniaschizophrenia
JPRN-jRCT2080223731Sumitomo Dainippon Pharma Co., Ltd.24
进行中(未招募)
不适用
A Study of Intravenous Mircera for the Treatment of Anemia in Pediatric Patients on Hemodialysis.Anemia associated with chronic kidney disease in pediatric patients (CKD) on hemodialysisMedDRA version: 17.0Level: LLTClassification code 10058124Term: Nephrogenic anemiaSystem Organ Class: 100000004851
EUCTR2007-007758-70-HUF. Hoffmann-La Roche Ltd68
进行中(未招募)
1 期
An open-label multi-center, multiple dose study to determine the optimum starting dose of intravenous MIRCERA® for maintenance treatment of anemia in pediatric patients with chronic kidney disease on hemodialysisAnemia associated with chronic kidney disease in pediatric patients (CKD) on hemodialysisMedDRA version: 9.1Level: LLTClassification code 10058124Term: Nephrogenic anemia
EUCTR2007-007758-70-FRF. Hoffmann-La Roche Ltd41
进行中(未招募)
不适用
A Study of Intravenous Mircera for the Treatment of Anemia in Pediatric Patients on Hemodialysis.Anemia associated with chronic kidney disease in pediatric patients (CKD) on hemodialysisMedDRA version: 17.0Level: LLTClassification code 10058124Term: Nephrogenic anemiaSystem Organ Class: 100000004851
EUCTR2007-007758-70-DEF. Hoffmann-La Roche Ltd68