A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of the Efficacy and Safety of Qifangfeixian Granules in the Treatment of Connective Tissue Disease-Associated Interstitial Lung Disease (CTD-ILD)

November 2, 2024 updated by: Huilan Zhang
Interstitial lung disease (ILD) is a heterogeneous group of diseases characterized by inflammation and/or fibrinization of the alveolar unit due to a variety of known or unknown causes. CTD-ILD is one of its common categories and includes any ILD with a definite diagnosis of connective tissue disease or with a set of symptoms, signs, and abnormalities suggested by laboratory examination. The incidence of CTD-ILD varies from home to abroad. Foreign studies indicate that the number of CTD-ILD in this study accounted for 34.8% of the total number of ILD in this study, while domestic studies indicate that the number of CTD-ILD in this study accounted for 67% of the total number of ILD. At present, the treatment of CTD-ILD includes hormone, immunosuppressant cyclophosphamide, mortemycophenate, tacrolimus, etc. The above treatment has great side effects, which may increase the risk of infection and the incidence of malignant tumor. Traditional Chinese medicine has unique advantages in alleviating the clinical symptoms of the disease, reducing the use of hormones and hormone complications, and preventing infection. Qifangfeixian granule is derived from "Fangji Huangqi Decoction" in the Summary of Golden Chamber. Modern pharmacology shows that Huangqi has the functions of regulating immunity, protecting liver, antibacterial and antiviral, etc. In order to further evaluate the effectiveness and safety of using Qifangfeixian granule (Huangqi, Fangji, dogwood, dodder, ginkgo, salvia miltiorrhizae, Taoren, etc.) in the treatment of CTD-ILD patients, Determined to explore a path of CTD-ILD treatment with Chinese characteristics, we hereby apply for a multicenter controlled clinical study.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

ILD is a common complication of CTD, with high disability rate and fatality rate, poor prognosis and high fatality rate. Ild is one of the main causes threatening the life of patients. The objective of this study was to evaluate the efficacy and safety of Qifangfeixian granules in the treatment of CTD-ILD patients, and to provide a new treatment plan for CTD-ILD patients. This is a randomized, placebo-controlled, multicenter study to evaluate the efficacy and safety of Qifangfeixian granules in the treatment of patients with fibrotic interstitial lung disease. The study drugs included Qifangfeixian Granule and placebo, which was identical in appearance, taste and weight with Qifangfeixian Granule, and were given 1 bag twice a day. This study planned to enroll 124 subjects, who were randomly assigned at a ratio of 1:1, with 62 subjects in each group. Subjects who met all the inclusion criteria and did not meet the exclusion criteria at baseline were randomly assigned to either of the following two groups: (1) Qifangfeixian Granule treatment group: orally administered with 1 bag of Qifangfeixian granule twice a day; (2) Placebo (PRO) control group: orally administered with 1 bag of placebo twice a day. If participants withdraw from the study early, they will be followed up for 4 weeks. Participants were allowed to make dose adjustments during treatment and were withdrawn from the study when a serious adverse event occurred or medication was discontinued due to an adverse event. Throughout the course of the study, safety checks and assessments will be conducted according to the time points specified in the protocol, including adverse events, HRCT, clinical laboratory tests (blood routine, blood biochemistry, urine routine, coagulation function, myocardial enzymes, etc.), 12-lead electrocardiogram, vital signs, and physical examination. Patient data were recorded on the case report form based on the visit.

Study Type

Interventional

Enrollment (Estimated)

124

Phase

  • Phase 2
  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • China
    • Hubei
      • Wuhan, Hubei, China, 430030
        • Recruiting
        • Tongji Hospital affiliated to Huazhong University of Science and Technology
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • 1. Male or female aged 18-80. 2. Both conditions (1) and (2) are met or conditions (3) are met:

    1. Diagnosis of CTD: CTD can be clearly diagnosed by referring to the classification criteria of each disease. SLE, SS, SSc, RA, PM/DM, etc. can be diagnosed according to the corresponding international classification standards.
    2. Diagnosis of ILD: Combined with the patient's symptoms such as progressive dyspnea, dry cough, pulmonary signs such as Velcro rales in both lungs, pulmonary function examination suggesting restrictive ventilation disorder and diffusion dysfunction, High-resolution CT of the chest indicated diffuse nodules, ground-glass changes, alveolar consolidation, thickening of interlobular septum, downline pleura, mesh shadows with cyst formation or cellular changes, tractive bronchiectasis, or structural changes of the lung.
    3. ILD (confirmed by high-resolution chest CT or surgical lung biopsy) is present, and ① other known etiology is excluded; ② A definite CTD cannot be diagnosed; (3) At least 2 of the following 3 characteristics: A. Clinical manifestations: (1) distal finger skin cracks (" technician hand "); (2) distal fingertip skin ulcer; (3) Inflammatory arthritis or polyjoint stiffness ≥60 min; (4) telangiectasia of the palm or finger abdomen; (5) Reynolds phenomenon; (6) unexplained swelling of the fingers; (7) Unexplained fixed rash of extended fingers (Gottron sign).

B. Serological manifestations: (1) ANA titer ≥ 1:320, diffuse type, spot type, homogeneous type, or ①ANA nucleolar type (arbitrary titer), or ②ANA centromere type (arbitrary titer); (2) Rheumatoid factor ≥2 times the upper limit of normal reference value; (3) Positive anti-CCP antibody; (4) Anti-double-stranded DNA antibody is positive; (5) Anti-SSA (Ro) antibody positive; (6) Anti-SSB (La) antibody positive; (7) Positive anti-ribonucleoprotein antibody; (8) Positive anti-SM antibody; (9) Anti-topoisomerase (Scl-70) antibody was positive; (10) Anti-TRNA synthase (such as Jo-l, PL-7, PL-12; Others include EJ, 0J, KS, Zo, tRS) antibody positive; (11) Anti-PM-SCL antibody is positive; (12) Anti-melanoma differentiation related gene 5 (MDA5) antibody was positive.

C. Morphological findings: (1) Chest high-resolution CT findings: ①NSIP, or ②OP, or ③NSIP overlapping OP, or ④LIP; (2) Pathological types of surgical lung biopsy: ①NSIP, or ②OP, or ③NSIP overlapping OP, or ④LIP, or ⑤ interstitial lymphocyte infiltration associated with hair center formation, or ⑥ diffuse lymphoplasmic cell infiltration (with or without lymphofollicular formation); (3) Multiple thoracic involvement (except interstitial pneumonia) : ① unexplained pleural effusion/pleural thickening; ② Unexplained pericardial effusion/pericardial thickening; (3) Endogenous airway diseases of unknown origin, including airflow obstruction, bronchiolitis, or bronchiectasis (confirmed by pulmonary function, imaging, or histopathology); ④ Pulmonary vascular disease of unknown cause.

Exclusion Criteria:

  • 1. When visiting 1, set AST and ALT to 1.5x ULN 2. Bilirubin > 1.5 x ULN at visit 1 3. At visit 1, creatinine clearance was < 30 mL/min as calculated by Cockcroft - Gault formula.

    4. Patients with underlying chronic liver disease (Child Pugh A, B, or C liver injury).

    5. Received other investigational medications within 1 month or 6 half-lives (whichever is greater) prior to the screening visit (visit 1).

    6. Significant pulmonary arterial hypertension (PAH) as defined by any of the following criteria: (1) clinical/echocardiographic evidence of prior significant right heart failure; (2) Medical history, including the right cardiac catheter showing cardiac index ≤2L/min/m2; (3) parenteral administration of eprostol/traprostacycline is required to treat PAH.

    7. Other lung abnormalities deemed clinically significant by the investigators. 8. Major extrapulmonary physical limitations (e.g., chest wall malformations, massive pleural effusion).

    9. Cardiovascular disease, any of the following: (1) severe hypertension within 6 months of visit 1, uncontrollable after treatment (≥160/100 mmHg); (2) myocardial infarction within 6 months of visit 1; (3) Unstable angina pectoris within 6 months of visit 1 10. History of severe central nervous system (CNS) events. 11. Known allergy to the experimental drug. 12. Other medical conditions that may interfere with the testing procedure or, as determined by the investigator, may interfere with trial participation or may put the patient at risk when participating in the trial.

    13. Women in this trial who are pregnant, breastfeeding or planning to become pregnant.

    14. Patients were unable to understand or follow trial procedures, including completing questionnaires on their own without assistance.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Qifangfeixian granule group
62 cases in the group , 2 times a day, each time 1 bag of Qifangfeixian granules, oral administration
Drug: Qifangfeixian granules
The experimental group was treated with Qifangfixian granules
Placebo Comparator: Placebo control group
62 control group patients were orally administered with 1 bag of placebo twice a day
Other: Placebo
The control group was treated with placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
forced vital capacity(FVC)
Time Frame: 12 weeks
Changes of FVC (ml) from baseline in the experimental group and the control group after 12 weeks of treatment with Qifangfeixian granules
12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
hormone dosage change
Time Frame: 12 weeks
Changes of hormone dosage from baseline in the experimental group and the control group after 12 weeks of treatment with Qifangfeixian granules
12 weeks
Pulmonary fibrosis survival symptom score
Time Frame: 12 weeks
Change of pulmonary fibrosis survival symptom score from baseline after 12 weeks of treatment with Qifangfeixian granules in experimental group and control group using L-PF questionnaire.
12 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
dyspnea scores
Time Frame: 12 weeks
Percentage decrease in dyspnea score from baseline after 12 weeks of treatment with Qifangfeixian granules in experimental group compared with control group
12 weeks
Forced expiratory volume in one second(FEV1)
Time Frame: 12 weeks
Percentage decrease in FEV1 from baseline after 12 weeks of treatment with Qifangfeixian granules in the experimental group compared with the control group
12 weeks
Chest CT
Time Frame: 12 weeks
Percentage decrease in chest CT score from baseline after 12 weeks of treatment with Qifangfeixian granules in experimental group compared with control group
12 weeks
Combined infection and acute exacerbation
Time Frame: 12 weeks
Evaluation of infection and acute exacerbation after 12 weeks of treatment with Qifangfeixian granules in experimental group and control group
12 weeks
Hospitalization or death from respiratory causes
Time Frame: 12 weeks
Time between trial and hospitalization or death due to respiratory causes in the experimental group compared with the control group
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Huilan Zhang

Investigators

  • Study Chair: Zhang Huilan, PD, Tongji hospital affiliated to huazhong university of science and technology, Wuhan, hubei

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 25, 2024

Primary Completion (Estimated)

May 20, 2027

Study Completion (Estimated)

June 1, 2027

Study Registration Dates

First Submitted

October 28, 2024

First Submitted That Met QC Criteria

November 2, 2024

First Posted (Estimated)

November 5, 2024

Study Record Updates

Last Update Posted (Estimated)

November 5, 2024

Last Update Submitted That Met QC Criteria

November 2, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Zhang huilan

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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