跳至主要内容
临床试验/EUCTR2004-000035-28-GB
EUCTR2004-000035-28-GB进行中(未招募)不适用

TDS-943 MAXIMUM USE TOLERANCE STUDY

Wyeth Consumer Healthcare0 个研究点目标入组 75 人开始时间: 2005年2月21日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
75

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

  • - Subject is cleared by a site-affiliated physician.
  • - Females are not pregnant or breast feeding.
  • 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
  • F.1.3 Elderly (>=65 years)
  • F.1.3.1 Number of subjects for this age range
  • - Subject is cleared by a site-affiliated physician.
  • - Females are not pregnant or breast feeding.
  • 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
  • F.1.3 Elderly (>=65 years)
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - history of any hypersensitivity (including asthma, rhinitis, or urticaria) to diclofenac
  • or to any of the excipients used in the topical spray, or to aspirin or any other NSAID, or to paracetamol;
  • - on chronic nonsteroidal anti-inflammatory drug therapy, defined as taking a daily
  • regimen 5 to 7 days/week;
  • - history (within the past 2 years) of a cutaneous reaction to any pharmaceutical
  • or non-pharmaceutical product;
  • - history of any hypersensitivity (including asthma, rhinitis, or urticaria) to diclofenac
  • or to any of the excipients used in the topical spray, or to aspirin or any other NSAID, or to paracetamol;
  • - on chronic nonsteroidal anti-inflammatory drug therapy, defined as taking a daily
  • regimen 5 to 7 days/week;
  • - history (within the past 2 years) of a cutaneous reaction to any pharmaceutical
  • or non-pharmaceutical product;

研究者

相似试验

进行中(未招募)
不适用
A Safety Study of TDS-943Of Product: Relieve pain and swelling in joints, muscles
EUCTR2004-001586-18-GBWyeth Consumer Healthcare75
进行中(未招募)
不适用
Phase I Study to Determine the Maximum Tolerated Dose of NC-6004 in Patients with Solid Tumours - Phase I dose-escalation Study of NC-6001 in patients with solid tumoursHistologically-confirmed advanced solid tumours for which no standard therapy exists or has failed therapy
EUCTR2005-004827-20-GBanoCarrier Co., Ltd.30
进行中(未招募)
1 期
Evaluation of ELX/TEZ/IVA in Cystic Fibrosis (CF) Subjects 2 Through 5 YearsMedDRA version: 20.0Level: PTClassification code 10011762Term: Cystic fibrosisSystem Organ Class: 10010331 - Congenital, familial and genetic disordersCystic Fibrosis
EUCTR2020-002251-38-DEVertex Pharmaceuticals Incorporated70
进行中(未招募)
1 期
A Phase III Study to Assess the Tolerability and Efficacy of MK-0822 (Odanacatib) in Reducing the Risk of Bone Metastases and Prolonging Disease-Free Survival in Women with Breast Cancer Spanish title: Estudio de Fase III para evaluar la tolerabilidad y eficacia de MK-0822 (Odanacatib) en la reducción del riesgo de desarrollar metástasis óseas y en la prolongación de la supervivencia libre de progresión en mujeres con cáncer de mama” - MK-0822 (Odanacatib) in Women with Breast CancerPrevention of disease recurrence in patients with breast cancer. Spanish indication: Prevención de recurrencia de la enfermedad en pacientes con cáncer de mamaMedDRA version: 9.1 Level: LLT Classification code 10005993 Term: Bone metastases
EUCTR2008-002119-42-ESMerck& Co., Inc.4,000
进行中(未招募)
1 期
A Phase III Study to Assess the Tolerability and Efficacy of MK-0822 (Odanacatib) in Reducing the Risk of Bone Metastases and Prolonging Disease-Free Survival in Women with Breast Cancer - MK-0822 (Odanacatib) in Women with Breast CancerPrevention of disease recurrence in patients with breast cancer.MedDRA version: 9.1Level: LLTClassification code 10005993Term: Bone metastases
EUCTR2008-002119-42-SKMerck& Co., Inc.4,000