跳至主要内容
临床试验/PER-114-11
PER-114-11未知未知

A 52-WEEK, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFECT OF ROFLUMILAST 500 μg ON EXACERBATION RATE IN SUBJECTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD) TREATED WITH A FIXED-DOSE COMBINATION OF LONG-ACTING BETA AGONIST AND INHALED CORTICOSTEROID (LABA/ICS)

Forest Research Institute, Inc,0 个研究点目标入组 71 人开始时间: 2012年3月1日最近更新:

试验速览

阶段
未知
入组人数
71

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
40 至 99(—)

入选标准

  • 1. MALE OR FEMALE SUBJECTS AT LEAST 40 YEARS OF AGE.
  • 2. HISTORY OF COPD (ACCORDING TO GOLD 2010) FOR AT LEAST 12 MONTHS PRIOR TO SCREENING (VISIT 1) ASSOCIATED WITH CHRONIC PRODUCTIVE COUGH FOR 3 MONTHS IN EACH OF 2 CONSECUTIVE YEARS (WITH OTHER CAUSES OF PRODUCTIVE COUGH EXCLUDED). ONLY SUBJECTS WITH CHRONIC BRONCHITIS WILL BE INCLUDED.
  • 3. FORCED EXPIRATORY VOLUME AFTER 1 SECOND (FEV₁)/FORCED VITAL CAPACITY (FVC) RATIO (POSTBRONCHODILATOR) < 70% AT SCREENING (VISIT 1).
  • 4. FEV₁ (POSTBRONCHODILATOR) ≤ 50% OF PREDICTED AT SCREENING (VISIT 1).
  • 5. AT LEAST TWO DOCUMENTED MODERATE OR SEVERE COPD EXACERBATIONS WIHTIN 12 MONTHS PRIOR TO SCREENING (VISIT 1).
  • 6. SUBJECTS MUST BE ON FDC LABA/ICS (ADVAIR® 250/50 μg 1 puff BID OR, SYMBICORT® 160/4,5 μg 2 puffs BID) CONCOMITANT TREATMENT ≥ 3 MONTHS PRIOR TO SCREENING (VISIT 1).
  • 7. THSE SUBJECTS WHO WERE PREVIOUSLY TREATED WITH LAMA MUST HAVE BEEN ON A STABLE DOSE FOR ≥ 3 MONTHS BEFORE SCREENING (VISIT 1) AND MUST CONTINUE ON THE SAME DOSE THROUGHOUT THE STUDY.
  • 8. FORMER SMOKER (DEFINED AS SMOKING CESSATION AT LEAST 1 YEAR AGO) OR CURRENT SMOKER BOTH WITH A SMOKING HISTORY OF AT LEAST 20 PACK-YEARS.

排除标准

  • 1. SEVERE OR VERY SEVERE COPD EXACERBATION AND/OR COPD EXACERBATIONS TREATED WITH ANTIBIOTICS OR SYSTEMIC GLUCOCORTICOSTEROIDS WITHIN 4 WEEKS OF SCREENING (VISIT 1) (ie, SUBJECTS MUST BE CLINICALLY STABLE).
  • 2. LOWER RESPIRATORY TRACT INFECTION WITHIN 4 WEEKS OF SCREENING (VISIT 1).
  • 3. DIAGNOSIS OF SIGNIFICANT LUNG DISEASE OTHER THAN COPD (eg., HISTORY OF PRIMARY BRONCHIECSTASIS, CYSTIC FIBROSIS, BRONCHIOLITIS, LUNG RESECTION, LUNG CANCER, INTERSTITIAL LUNG DISEASE [eg., FIBROSIS, SILICOSIS, SARCOIDOSIS], OR ACTIVE TUBERCULOSIS, PULMONARY THROMBOEMBOLIC DISEASE), PULMONARY RESECTION OR LUNG VOLUME SURGERY DURING THE PAST 12 MONTHS, CYSTIC FIBROSIS, KARTAGENER SYNDROME) POST ORGAN TRANSPLANTATION, OR WHO ARE EXPECTED TO REQUIRE THORACOTOMY OR OTHER LUNG SURGERY DURING THE STUDY.
  • 4. KNOWN ALFA-1-ANTITRYPSIN DEFICIENCY.
  • 5. CURRENT DIAGNOSIS OF ASTHMA (EITHER CONTROLLED OR UNCONTROLLED).
  • 6. LIVER IMPAIRMENT CHILD-PUGH B OR C AND/OR ACTIVE VIRAL HEPATITIS.
  • 7. CHRONIC USE OF OXYGEN THERAPY ≥ 15 hours/day
  • 8. BODY MASS INDEX (BMI) ≥ 45 kg/m²

研究者

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