Efficacy and Safety of Pirfenidone in Patient With Systemic Sclerosis-associated Interstitial Lung Disease

Inclusion Criteria:

1.Female or male subjects aged between 18 and 75 years of age. 2.2013 ACR / EULARclassification criteria for SSc fulfilled. 3.SSc disease onset (defined by firstnon-Raynaud symptom) within 5 years. 4.SSc related Interstitial Lung Disease confirmed byHRCT. 5.Forced vital capacity (FVC) 40% to 70% predicted(include 40% and70% ). 6.Subjecthave the ability to understand and sign the informed consent before the trials.

Exclusion Criteria:

1. Subjects not fulfill all of the above inclusion criteria.

2. AST, ALT >1.5 x ULN.

3. Bilirubin >1.5 x ULN.

4. Creatinine clearance <30 mL/min.

5. Airway obstruction (pre-bronchodilator FEV1/FVC <0.7).

6. Other clinically significant pulmonary abnormalities.

7. Allergic to test drugs or components (e.g. lactose).

8. Clinical Significant Pulmonary hypertension:.

9. Significant past clinical evidence or echocardiography of right heart failure.

10. History of right heart catheterization showed that cardiac index ≤ 2 l/min/m2.

11. Pulmonary hypertension, which needs to use EPoprostenol/ Treprostinil forparenteral treatment .

12. Cardiovascular diseases:

13. Six weeks in severe hypertension, and out of control aftertreatment(≥160/100mmHg).

14. Myocardial infarction within six months.

15. A period of 6 months in unstable angina.

16. More than 3 digital fingertip ulcers or a history of severe digital necrosis requiringhospitalization or severe other ulcers.

17. Bleeding risk, including the following criterias: a. Predisposition to bleeding. b.Subjects need to the following treatments:i.Fibrinolysis, full-dose anticoagulation therapy(such as vitamin K antagonists,direct thrombin inhibitor, heparin, Hirudin ). ii. High dose antiplatelet therapy[Note: not prohibited to maintain equipment neededindwelling venous pathway prophylactic low dose of heparin or heparin fluid (e.g.enoxaparin, daily 4000 I.U. s.c.) and the prevention of the use of antiplatelettherapy (e.g. acetylsalicylic acid, until 325 mg/d, or other antiplatelet dose of 75mg/d the same dose of clopidogrel, or treatment)]. c.history of hemorrhagic central nervous system (CNS) event within last year. d. Anyof the following conditions within 3 months: i.Hemoptysis or hematuria ii. Activegastrointestinal bleeding or gastrointestinal ulcer. iii. major trauma or majorsurgery (researchers determined). e.coagulation parameters:international normalisedratio (INR) >2, prolongation of prothrombin time (PT) and partial thromboplastin time (PTT) by >1.5 x ULN)

18. May interfere with detection procedures (such as interrupt oxygen intolerance inpulmonary function tests) or based on the researchers estimate, may affect the test toparticipate in or participate in the test may put patients at risk of disease or othercomplications (such as caused by SSc severe gastrointestinal symptoms).

19. Researchers determined that life expectancy was due to other diseases (non SSc) for aperiod of up to 2.5 years.

20. Clinical signs of malabsorption or needing parenteral nutrition.

21. History of thrombotic event within last year(Including stroke and transient ischemicattack).

22. Previous treatment with nintedanib or pirfenidone.

23. Use the following medicine:

24. Treatment with prednisone >10 mg/day within 2 weeks.

25. Treatment with azathioprine, hydroxychloroquine, colchizine, D-penicillamine,sulfasalazine within 8 weeks .

26. Treatment with cyclophosphamide, rituximab, tocilizumab, abatacept, leflunomide,tacrolimus, newer anti-arthritic treatments like tofacitinib and ciclosporine A,potassium para-aminobenzoate within 6 months.

27. Unstable background therapy with cyclophosphamide or mycophenolate mofetil / sodium ormethotrexate (not allow treatment). Patients must or A. patients cannot receiveimmunosuppressive therapy, sodium cyclophosphamide or mycophenolate mofetil / or MTXstable or B. within 6 months of acceptance, and in at least 6 months afterrandomization, the treatment to keep the background stable (exclusion criteria 16 and 17 and the combined use of early precautions).

28. Previous or planned hematopoietic stem cell transplantation next year.

29. Major surgery is planned during the treatment period.

30. Pregnancy or lactation or make a schedule during the trials.

31. Give the drug 28 days before or after administration of the 3 month period, women ofchildbearing age * are unwilling or unable to use contraceptive methods highlyeffective (according to ICH M3 (R2)), a highly effective means in the correct andconsistent application of a barrier method when the failure rate of less than 1% peryear. * women of childbearing age is defined has undergone menarche and in line with "infertile women" standard "[female infertile women" is defined as: postmenopausalperiod (12 months without menstruation, no other medical reasons) or permanentsterilization (e.g., tubal occlusion, hysterectomy, bilateral ovarian resection orbilateral tubal resection women)].

(23)According to the researchers,exhibited evidence of alcohol or drug abuse. (24)Patientswho were unable to understand or comply with the procedure were included in theself-administered questionnaire, which was completed without help.

25.Patients with underlying chronic liver disease (Child Pugh A, B, C hepatic impairment).

26.Clinical signs of malabsorption or needing parenteral nutrition. 27.With active pepticulcer. 28.With mental illness . 29.Within 3 months to participate in other clinical trials. 30.Researchers determined that they did not participate in the trial.