跳至主要内容
临床试验/JPRN-jRCT2080220747
JPRN-jRCT2080220747未知3 期

A Phase 3, randomized, double-blind, double-dummy, parallel group, multi-center, multi-national study for evaluation of efficacy and safety of DU-176b versus warfarin in subjects with atrial fibrillation - Effective aNticoaGulation with factor xA next GEneration in Atrial Fibrillation (ENGAGE AF-TIMI 48)

DAIICHISANKYO Co.,Ltd., DAIICHI SANKYO PHARMA DEVELOPMENT0 个研究点目标入组 20,500 人开始时间: 2009年6月12日最近更新:
适应症

试验速览

阶段
3 期
发起方
入组人数
20,500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 21age old 至 ot applicable(—)
性别
All

入选标准

  • Documented AF on ECG

排除标准

  • - Subjects with any contraindication for anticoagulant agents
  • - Subjects with conditions associated with high risk of bleeding
  • - Females of childbearing potential

研究者

发起方
DAIICHISANKYO Co.,Ltd., DAIICHI SANKYO PHARMA DEVELOPMENT

相似试验

招募中
1 期
A Phase 3 study to assess efficacy and safety of oral tebipenem compared to IV imipenem-cilastatin in adults with cUTI/APcomplicated urinary tract infection (cUTI) or acute pyelonephritis (AP)MedDRA version: 20.0Level: PTClassification code: 10046571Term: Urinary tract infection Class: 100000004862
CTIS2023-503785-22-00Spero Therapeutics Inc.2,648
进行中(未招募)
不适用
A Phase 3, randomized, double-blind, double-dummy, parallel-group, multi-center, multi-national study for evaluation of efficacy and safety of DU-176b versus warfarin in subjects with atrial fibrillation - Effective aNticoaGulation with factor xA next GEneration in Atrial Fibrillation (ENGAGE-AF) - NDMedDRA version: 9.1Level: LLTClassification code 10003658Term: Atrial fibrillationAtrial fibrillation
EUCTR2008-004522-16-ITDAIICHI SANKIO DEVELOPMENT LIMITED16,500
尚未招募
3 期
A Study of Oral Tebipenem Pivoxil Hydrobromide (TBP-PI-HBr) Compared to Intravenous Imipenem-cilastatin in Participants With Complicated Urinary Tract Infection (cUTI) or Acute Pyelonephritis (AP)
CTRI/2024/05/067164PSI CRO Pharma India Pvt Ltd
进行中(未招募)
不适用
ate development study which compares the effectiveness and safety of a not yet approved drug called edoxaban versus a widely-used andapproved drug called warfarin in patients suffering from blood clots inlegs and/or in lungs. The study is double-blind (that is when neither the patient nor the investigator know which of the 2 drugs the patient is receiving) and is being conducted in many countries around the worldReduction of the risk of symptomatic recurrent venous thromboembolic complications in patients with acute symptomatic deep vein thrombosis (DVT) and/or pulmonary embolism (PE)MedDRA version: 14.1Level: PTClassification code 10037377Term: Pulmonary embolismSystem Organ Class: 10038738 - Respiratory, thoracic and mediastinal disordersMedDRA version: 14.1Level: PTClassification code 10051055Term: Deep vein thrombosisSystem Organ Class: 10047065 - Vascular disorders
EUCTR2009-014290-40-EEDaiichi Sankyo Development Limited7,500
进行中(未招募)
1 期
A phase 3, randomized, double-blind, double-dummy, parallel-group, multi-center, multi-national study for the evaluation of efficacy and safety of (LMW) heparin/edoxaban versus (LMW) heparin/warfarin in subjects with symptomatic deep-vein thrombosis and/or pulmonary embolism - Evaluation of edoxaban vs. warfarin in subjects with symptomatic venous thromboembolism (VTE)Reduction of the risk of symptomatic recurrent venous thromboembolic complications in patients with acute symptomatic deep vein thrombosis (DVT) and/or pulmonary embolism (PE)MedDRA version: 12.0Level: LLTClassification code 10037377Term: Pulmonary embolismMedDRA version: 12.0Level: LLTClassification code 10051055Term: Deep vein thrombosis
EUCTR2009-014290-40-FRDaiichi Sankyo Development Limited7,500