Safety, Tolerability and Efficacy of VUM02 Injection in Treatment of Idiopathic Pulmonary Fibrosis (IPF)

Launched by WUHAN OPTICS VALLEY VCANBIOPHARMA CO., LTD. · Jan 19, 2024

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called VUM02 Injection for patients with Idiopathic Pulmonary Fibrosis (IPF), a lung disease that causes scarring in the lungs, making it hard to breathe. The researchers want to see if this treatment is safe, how well people tolerate it, and if it shows any early signs of being effective. VUM02 is made from special cells derived from human umbilical cords, and patients will receive this injection multiple times over a short period.

To participate in this trial, individuals must be between 40 and 75 years old and have a confirmed diagnosis of IPF. They should have stable lung function and have been on standard treatments for at least three months. The trial is currently looking for participants, and those who join can expect to receive the injections every three days for a total of three times while being closely monitored for any side effects. This study is an important step in exploring new options for IPF patients, especially for those who have not found relief with existing treatments.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• Patients must meet all of the following criteria to be eligible for this trial:
• • 1. Gender unrestricted, aged between 40 and 75 years old (inclusive);
• • 2. Diagnosed with IPF according to the 2022 Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults: An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline.
• • 3. In the 3 months prior to administration, determined by the investigator to have stable disease, with diffusing capacity of the lung for carbon monoxide (DLCO) between 30% and 79% of the predicted value (adjusted for Hb), FVC/predicted ≥50%, and forced expiratory volume in one second (FEV1)/FVC ≥0.70;
• • 4. Allowed to enroll are the patients who have been treated according to the current standard treatment plan for IPF and have maintained the treatment for at least 3 months;
• • 5. Good compliance, able to understand and cooperate with pulmonary function test procedures, willing to participate voluntarily in the trial according to the protocol requirements, and understand and sign the informed consent form voluntarily.
• Exclusion Criteria:
• Patients meeting any of the following criteria are not eligible for this trial:
• • 1. Allergic to any ingredient of the product;
• • 2. Suffering from interstitial lung diseases (ILD) other than IPF, including but not limited to: any other type of interstitial pneumonia; lung diseases related to exposure to fibrogenic agents or other environmental toxins or drugs (such as amiodarone, bleomycin, or methotrexate); other types of occupational lung diseases; granulomatous lung diseases; systemic diseases including vasculitis, infectious diseases (i.e., tuberculosis), and connective tissue diseases, or a history of prior pulmonary resection;
• • 3. During the screening period, having any of the following pulmonary diseases: asthma, pulmonary embolism, pneumothorax; lung cancer, obstructive bronchitis, or other active lung diseases; a known history of immune system diseases (such as thymic diseases, systemic lupus erythematosus); acquired or congenital immunodeficiency diseases, or a history of organ transplantation;
• • 4. Chest HRCT during the screening period shows emphysema area \> fibrosis area;
• • 5. Previously received stem cell therapy or intolerant to cell therapy;
• • 6. Received unstable standard of care for IPF within the 3 months prior to screening;
• • 7. Used non-biological drugs with cell proliferation inhibition or immunosuppressive/immunomodulatory effects during the 3 months prior to screening, such as Mycophenolate Mofetil, cyclophosphamide, tacrolimus, and JAK inhibitors, as well as other Chinese herbal medicines with immunomodulatory effects;
• • 8. Used biologics such as rituximab, TNF-α monoclonal antibodies, and IFN-γ monoclonal antibodies within the 6 months prior to screening;
• • 9. Used anticoagulant drugs, sildenafil, bosentan, macitentan, imatinib, and other drugs for treating IPF within the 4 weeks prior to screening;
• • 10. Participated in interventional clinical studies within the 3 months or within the half-life of 5 drugs (whichever is longer) before screening;
• • 11. Hospitalized 2 or more times in the past year due to acute exacerbation of IPF;
• • 12. Had a lung infection within the past month;
• • 13. Had a history of invasive or non-invasive mechanical ventilation, or currently require oxygen therapy (oxygen therapy time \>15 h/d);
• • 14. Smoked within the past 3 months or cannot quit smoking during the trial;
• • 15. The expected survival period may be less than 1 year judged by investigator;
• • 16. Laboratory tests meet any of the following criteria: white blood cell count less than 3.5×109/L or neutrophils less than 1.5×109/L for any reason; hemoglobin (HGB) ≤90 g/L; fibrinogen (FIB) ≤0.5×LLN; alanine aminotransferase (ALT) \>2×ULN, aspartate aminotransferase (AST) \>2×ULN, total bilirubin (TBIL) \>1.5×ULN, direct bilirubin (DBIL) \>1.5×ULN, blood creatinine (Cr) \>1.5×ULN;
• • 17. Evidence suggests that the subject currently has digestive system, urinary system, cardiovascular system, hematological system, nervous system, psychiatric, or metabolic diseases that may affect safety, such as severe kidney disease requiring blood dialysis or peritoneal dialysis; advanced hepatitis or cirrhosis; severe heart failure (NYHA Grade III and IV); poorly controlled hypertension (≥180/100 mmHg); severe pulmonary heart disease or pulmonary arterial hypertension considered by the investigators to affect the evaluation of the trial results;
• • 18. Have various malignant tumors or a history of malignant tumors;
• • 19. 12-lead electrocardiogram shows severe arrhythmias (such as ventricular tachycardia, frequent supraventricular tachycardia, atrial fibrillation, and atrial flutter) or degree II and above atrioventricular block;
• • 20. Positive results in serological tests (HBsAg, HCV antibodies, HIV antibodies, syphilis spirochete antibodies), among which carriers of hepatitis B virus, stable patients with hepatitis B (DNA titer ≤2000 IU/mL or copy number \<1000 copies/mL) after drug treatment, and cured patients with hepatitis C (negative HCV RNA) can be enrolled after being judged eligible by the investigator;
• • 21. Pregnant or lactating women, or those with a positive result in the screening period for beta-human chorionic gonadotropin (β-HCG) testing; or male subjects of childbearing potential and female subjects of childbearing age who are unable and unwilling to take effective non-drug contraceptive measures during the study and 6 months after the end of the study;
• • 22. Subjects deemed inappropriate for entry into this study by the investigator.