Clinical Study of Allogeneic Adipovarian Active Protein in the Treatment of Severe Idiopathic Pulmonary Fibrosis — CEFFE-IPF  

Idiopathic Pulmonary Fibrosis Clinical Trial

Official title: Clinical Study of Allogeneic Adipovarian Active Protein in the Treatment of Severe Idiopathic Pulmonary Fibrosis

Status Recruiting

Clinical Trial Summary

The goal of this clinical trail is to study the efficacy and safety of allogeneic adipocyclical active protein in the treatment of severe idiopathic pulmonary fibrosis. The main questions it aims to answer are: 1. Efficacy of allogeneic adipromic active protein in the treatment of severe idiopathic pulmonary fibrosis 2. Safety of allogeneic adipovularic active protein in the treatment of severe idiopathic pulmonary fibrosis. A total of 7 participants will be enrolled. Participants will be asked that they will receive 2ml of each nebulized inhalation Cell Free Fat Extract (CEFFE), inhaled every 3 days, for a total of 7 nebulized inhalation treatments. The clinical trial was designed using a single-center, self-controlled trial with no control group and no blinding.

Clinical Trial Description

1. Research purpose: Main Objective: To study the efficacy and safety of allogeneic adipocyclical active protein in the treatment of severe idiopathic pulmonary fibrosis, and the main observation and evaluation indicators include: clinical efficacy, clinical adverse events and laboratory abnormalities. The basis of the question: Animal experiments have found that Cell Free Fat Extract (CEFFE) has a certain improvement effect in bleomycin-induced mouse pulmonary fibrosis model. At present, domestic clinical studies have found that Cell Free Fat Extract (CEFFE) is safe for the treatment of human diseases without obvious side effects. Therefore, in this study, the Cell Free Fat Extract (CEFFE) was inhaled by nebulized inhalation for the treatment of severe idiopathic pulmonary fibrosis, and its efficacy and safety were observed. 2. Research Design: Overall design: single-center, self-controlled trial design was adopted, no control group was established, and blinding was not used. Number of planned cases: 7. Indications: severe idiopathic pulmonary fibrosis. 3. Clinical trails process: 3.1 Sign the informed consent form and collect relevant clinical data; For patients with a definitive diagnosis of severe idiopathic pulmonary fibrosis 3.2 Allogeneic Cell Free Fat Extract (CEFFE) treatment process: 3.2.1 Preparation of CEFFE of allogeneic origin: Healthy donors undergoing liposuction at the Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, sign a written informed consent. By a healthy donor under local anesthesia, inject swelling fluid into the abdomen, operate with a 20mL syringe or mechanical negative pressure machine (auxiliary liposuction methods such as laser, ultrasound and microwave cannot be added), determine the group according to the order of enrollment, and extract fat according to the required dose, and the single liposuction amount should be 150ml -200ml. The collected adipose tissue was rinsed with normal saline, allowed to stand, and centrifuged in a centrifuge at 1200g for 3min. After centrifugation, excess water at the bottom is removed, collected in a sterile 50mL syringe, stored, and transferred. Preparation of adipose tissue active factors is performed in the laboratory and cryopreservation. Two 10mL syringes connected by tee tubes, mechanically emulsified 60 times, collected into 50mL centrifuge tubes, centrifuged at 2000g for 5min. After centrifugation, the bottom transparent liquid layer was collected and filtered through a 0.22um filter to obtain fat decellularization active protein, which was frozen in a -20 °C freezer. 3.2.2 Health Donor Selection Criteria: 3.2.2.1 Age 18-45, male or female 3.2.2.2 Liposuction at the Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine 3.2.2.3 Sign the informed consent form for biological sample donation 3.2.3 Exclusion Criteria: 3.2.3.1 Patients with hepatitis B, hepatitis C, HIV, syphilis, cytomegalovirus, herpesvirus and other infections 3.2.3.2 Patients with severe hypertension, diabetes, heart disease and other chronic diseases 3.2.3.3 Patients with tumors or previous history of tumors 3.3 After negative percutaneous test, allogeneic CEFFE is inhaled by nebulization; 0.2ml CEFFE was injected intradermally 1 cm above the palmar stria on the palmar side of the right forearm, and 0.2ml of normal saline was injected intradermally 1 cm above the palmar stria on the palmar side of the left forearm as a control. Interpretation of skin test results: local pichu bulge, and red halo hard lump, diameter > 1 cm is positive. Give a single dose of 2ml allogeneic CEFFE stock solution (protein concentration of 3mg/ml), administered by nebulization inhalation, 8 minutes between each atomization time, 3 days apart; A total of 7 doses were given. 3.4 Observe the clinical symptoms, chest CT, lung function and related adverse reactions of patients at 1, 3, 6 and December after the end of allogeneic fat decellularization active protein treatment. 4. Evaluation Criteria: 4.1 Efficacy criteria: 4.1.1 Obvious effect means that the main symptoms and signs are significantly relieved, and the objective indicators are significantly improved. 4.1.2 Effective means that the main symptoms and signs have improved, and the objective indicators have improved. 4.1.3 Ineffective means that the main symptoms and signs have not changed, and the objective indicators have not changed significantly or worsened. 4.2 Safety evaluation: Clinical adverse events and laboratory tests are definitely related to allogeneic CEFFE treatment, likely related to allogeneic CEFFE treatment, may be related to allogeneic CEFFE treatment, may not be related to allogeneic CEFFE treatment, and may not be related to allogeneic CEFFE treatment. 4.3 Evaluation endpoints: Clinical efficacy, comprehensive efficacy and safety evaluation at 1, 3, 6 and 12 months after the end of treatment were the main evaluation endpoints. 5. Quality assurance of clinical trial data The quality control of this clinical trial is controlled and controlled by the Ninth People's Hospital affiliated to Shanghai Jiao Tong University School of Medicine, and the research work is carried out in accordance with GCP, SOP and quality control requirements. Develop a clinical research plan. GCP training for relevant researchers participating in the trial. 5.1 Before the start of the trial, the plan should be submitted to the Ethics Committee of the Ninth People's Hospital affiliated to Shanghai Jiao Tong University School of Medicine for approval; 5.2 in accordance with GCP guidelines, necessary steps should be taken during the design and implementation phases of the study to ensure that the data collected is accurate, consistent, complete and credible; 5.3 The participating researchers will strictly follow China's GCP standards to conduct the trial, collect and record the contents of the case report form truthfully, carefully and in detail in accordance with the clinical trial standard operating procedures (SOP), and verify them to ensure the reliability of the data; 5.4 The investigator fills in the information required by the protocol into the Case Report Form (CRF), and the supervisor verifies that it is complete and accurate, and instructs the staff of the research center to make necessary corrections and supplements; 5.5 All kinds of instruments, equipment, reagents, standards, etc. used in various inspection items in clinical trials should have strict quality standards and ensure that they work under normal conditions; 5.6 Send statistical issues in the test plan to statistical experts for review and check; 5.7 During the trial, the investigator monitors the research process, informed consent, and the correctness and completeness of the data in the case report form (CRF). 6. Recording and preservation of research materials In accordance with the GCP principle, the investigator should keep all the detailed original files of the subjects, and record the relevant test process, medication, laboratory test data, safety data and efficacy evaluation in the case report form, and the recorded data should be complete, timely and clear. Case report forms, original documents, medical records, etc. should be clear, detailed and easily identifiable by personnel participating in this clinical trial. At a minimum, the principal investigator must sign the inclusion confirmation page and completion page of the case report form to confirm the accuracy and completeness of all data. The case report form and the original file can only be modified by the investigator. Any changes to the case report form and the original file must not erase the original data. The correct modification method is to draw a single line on the original data, and then write the modified data next to the original data, and sign the date and the initials of the person who modified it. Test data should be retained for 10 years after the end of the test. However, if required by current regulations or agreements with sponsors, these data should be kept for a longer period of time. 7. statistical treatment scheme 7.1 filling in the case report form (CRF) The investigator should complete the filling of case report form in time, modify it according to the correct modification method, and the completed case report form shall be reviewed and signed by the main researchers 7.2 statistical analysis method and statistical description 7.2.1 Treatment of missing value of main efficacy index data: when some subjects lack a major efficacy data, the method of filling deficiency is determined from the statistical and professional perspective. If the case is missing, the data of the previous measurement shall be transferred. 7.2.2 Case analysis of incomplete test: the reasons for exfoliation should be analyzed one by one. 7.2.3 Descriptive statistics: mean, standard deviation, maximum value, minimum value, median, confidence interval, frequency (composition ratio), etc. 7.3 Statistical expression 7.3.1 The report mainly uses tables to show that the tables are self-evident, that is, they have table questions, table notes and examples. 7.3.2 The results of repeated measurement data are expressed in tables and statistical charts are attached to increase readability. 7.4 Statistical software SAS 9.1.3 and Das for clinical trial 3.0 software were used to analyze the software simultaneously, and the results were confirmed. 8. Modification and interim analysis in the course of the test Once the research plan has been discussed by the research group and reviewed by the ethics committee, it is not allowed to change at will; before the modification is implemented, the researcher must report the content and reason of the modification to the ethics committee of clinical trial for approval, and then carry out the research according to the modified scheme. ;

Related Conditions & MeSH terms

• Fibrosis
• Idiopathic Pulmonary Fibrosis
• Pulmonary Fibrosis

• NCT number: NCT05883293
• Study type: Interventional
• Source: Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
• Contact: WeiNing Xiong, Doctor
• Phone: 86-021-23271699
• Email: xiongdoctor@qq.com
• Status: Recruiting
• Phase: Early Phase 1
• Start date: June 1, 2023
• Completion date: December 31, 2024