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临床试验/EUCTR2015-000392-28-NL
EUCTR2015-000392-28-NL进行中(未招募)1 期

A double blind, randomised, placebo-controlled trial evaluating efficacy and safety of oral nintedanib treatment for at least 52 weeks in patients with Systemic Sclerosis associated Interstitial Lung Disease (SSc-ILD) - Nintedanib in SSc-ILD

Boehringer Ingelheim bv0 个研究点目标入组 750 人开始时间: 2015年8月24日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
750

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

  • - Age >= 18 years
  • - 2013 ACR / EULAR classification criteria for SSc fulfilled
  • - SSc disease onset (defined by first non-Raynaud symptom) within 7 years
  • - SSc related Interstitial Lung Disease confirmed by HRCT; Extent of fibrotic disease in the lung >= 10%
  • - FVC >= 40% of predicted normal
  • - DLCO 30% to 89% of predicted normal
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 450
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 70

排除标准

  • - AST, ALT >1.5 x ULN
  • - Bilirubin >1.5 x ULN
  • - Creatinine clearance <30 mL/min
  • - Airway obstruction (pre-bronchodilator FEV1/FVC <0.7)
  • - Other clinically significant pulmonary abnormalities
  • - Significant pulmonary hypertension
  • - Cardiovascular diseases
  • - More than 3 digital fingertip ulcers
  • - Bleeding risk (such as predisposition to bleeding, fibrinolysis, full-dose anticoagulation, high dose antiplatelet therapy, history of hemorrhagic central nervous system (CNS) event within last year
  • - international normalised ratio (INR) >2, prolongation of prothrombin time (PT) and partial thromboplastin time (PTT) by >1.5 x ULN)
  • - History of thrombotic event within last year
  • - Clinical signs of malabsorption or needing parenteral nutrition
  • - Previous treatment with nintedanib or pirfenidone
  • - Treatment with prednisone >10 mg/day, azathioprine, hydroxychloroquine, colchizine, D-penicillamine, sulfasalazine, cyclophosphamide, rituximab, tocilizumab, abatacept, leflunomide, tacrolimus, newer anti-arthritic treatments like tofacitinib and ciclosporine A, potassium para-aminobenzoate
  • - Unstable background therapy with either mycophenolate mofetil or methotrexate
  • - Previous or planned hematopoietic stem cell transplantation
  • - Patients with underlying chronic liver disease (Child Pugh A, B, C hepatic impairment)
  • - Patients with a history of Scleroderma Renal Crisis

研究者

发起方
Boehringer Ingelheim bv

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