Overview

A Multicenter Randomized Double-blind Clinical Study Evaluated the Safety, Pharmacokinetic and Pharmacodynamic Characteristics of Roflumilast in COPD Patients

Status:
Terminated
Trial end date:
2018-06-13
Target enrollment:
0
Participant gender:
All
Summary
To evaluate the safety and pharmacokinetics of different dose roflumilast in China COPD patient.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Jiangsu Chia-tai Tianqing Pharmaceutical Co.,Ltd
Criteria
Inclusion Criteria:

1. Is male or female and aged 40 or olderThe BMI≥ 19.0 kg/m2;

2. The patient with severe to very severe COPD as difine by the 2015 Gold strategy
.(postbronchodilator ≤0.7,,and a postbronchodilator FEV1≤50% predicted);

3. Has a history of chronic obstructive pulmonary disease (COPD) (according to Global
Initiative for Chronic Obstructive Lung Disease (GOLD) 2015) for at least 12 months
prior to Screening (Visit V0), At least two documented moderate or severe COPD
exacerbations within 12 months prior to Screening (Visit 0);

4. Must be a former smoker (defined as smoking cessation at least one year ago) or
current smoker both with a smoking history of at least 10 pack years;

5. Women of childbearing age must take reliable contraceptive measures

6. Signed informed consent

Exclusion Criteria:

1. Severe or very severe COPD exacerbations is still exist in screen visit(V0);

2. Lower respiratory tract infection not resolved 4 weeks prior to the baseline visit V0;

3. History of asthma diagnosis in patients < 40 years of age or relevant lung disease
other than COPD;

4. relevant lung disease other than COPD,as: Bronchiectasis, Cystic fibrosis, capillary
bronchitis, lung resection, lung cancer, interstitial lung disease and active
tuberculosis

5. Current participation in a pulmonary rehabilitation program or completion of a
pulmonary rehabilitation program within 3 months preceding the baseline visit V0

6. Known alpha-1-antitrypsin deficiency;

7. Clinically significant abnormal Laboratory examination,may due to one Undiagnosed
disease

8. The patient with severe Mental or neurological disease;

9. Has a history with Suicidal ideation or depression;

10. Congestive heart failure New York Heart Association Functional Classification (NYHA)
severity grade III-IV;

11. Used disabled combination medicine;

12. A serious autoimmune disease;

13. Liver dysfunction according to Child-Pugh B/C;

14. Serious acute Infectious diseases;

15. Has a history Malignant in the last 5 years;