Clinical Study on the Treatment of Type 1 Diabetes With CNK-UT009 Cell Injection

Launched by ZIBO CENTRAL HOSPITAL · Jul 3, 2025

Keywords

ClinConnect Summary

This clinical trial is testing a new treatment called CNK-UT009 cell injection for people with type 1 diabetes, a condition where the body’s immune system attacks the cells that make insulin. The main goals of the study are to see if the treatment is safe, to find the right dose, and to check if it might help improve diabetes management. Researchers will also study how the treatment affects the immune system and how the body processes the injected cells.

Adults aged 18 to 65 with type 1 diabetes who still produce a small amount of insulin and have certain diabetes-related antibodies may be eligible to join. Participants should have stable health without serious complications like severe infections or heart problems. If you join, you can expect regular medical check-ups, blood tests, and monitoring to track your response to the treatment and any side effects. Women who can become pregnant and their partners will need to use birth control during the study and for six months afterward. This study is currently recruiting volunteers, and those interested should be willing to follow the study procedures and provide informed consent.

Gender

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Eligibility criteria

• • Inclusion criteria
• Patients who meet all of the following criteria can be considered for inclusion:
• • Age 18 to 65 years old (including the cut-off value), gender not limited;
• • Diagnosed with autoimmune type 1 diabetes (meeting the diagnostic criteria of the "Chinese Guidelines for the Diagnosis and Treatment of Type 1 Diabetes (2021 Edition)"), and the peak C-peptide was ≥0.2nmol/L after 2-hour mixed meal (MMTT) stimulation during the screening period;
• • At least one insulin autoantibody is positive, such as glutamate decarboxylase autoantibody (GADA), protein tyrosine phosphatase autoantibody (IA-2A), insulin autoantibody (IAA) (without insulin use or within 2 weeks of insulin treatment), zinc transporter antibody (ZnT8A);
• • Glycated hemoglobin (HbA1c) ≥6.5% and ≤10.5%;
• • Body mass Index (BMI)≥18kg/m ² and ≤35kg/m ²;
• * Have sufficient organ and bone marrow functions, and the laboratory test values within 7 days before enrollment meet the following requirements, as detailed below:
• • Blood routine: Absolute neutrophil count (ANC) ≥1.0× 109 /L; Absolute lymphocyte count (LYC) ≥1.0× 109 /L; Platelet count (PLT) ≥75×109/L; Hemoglobin content (HGB) ≥80g/L; Heart: Left ventricular ejection fraction (LVEF) ≥50%; Cardiac function grade 1-2 Lung function: Indoor blood oxygen saturation ≥92%; Liver function: Serum total bilirubin (TBIL) ≤1.5×ULN; Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤3×ULN; Renal function: Serum creatinine (Cr) ≤1.5×ULN; Glomerular filtration rate (eGFR) ≥60mL/min/1.73m2 (calculated by the MDRD formula)
• • For female patients of childbearing age, the serum or urine pregnancy result must be negative before enrollment, and they must agree to take acceptable measures to minimize the possibility of pregnancy during the trial. Female patients of childbearing age or male patients whose sexual partners are female patients of childbearing age need to take effective contraceptive measures throughout the treatment period and 6 months after the last medication.
• • Agree to abide by the principles and suggestions of medical nutrition therapy in the "Chinese Guidelines for the Diagnosis and Treatment of Type 1 Diabetes Mellitus (2021 Edition)";
• • Voluntarily participate in clinical research, understand and be informed of this study, sign the informed consent form, and be willing to follow all trial procedures.
• • Exclusion criteria
• Patients meeting any of the following criteria are not eligible for enrollment:
• • Active malignant tumors requiring treatment, except for non-melanoma skin cancer or carcinoma in situ (such as breast, cervical);
• • Subjects who have received organ transplants in the past or are preparing to receive organ transplants;
• • Those who have received immunosuppressant treatment within 4 weeks before enrollment and/or require long-term immunosuppressive treatment during the study period, and are allowed to use topical, inhaled or intranasal corticosteroids intermittently;
• • Any life-threatening bleeding events occurred within 3 months before enrollment, including the need for blood transfusion treatment, surgery or local treatment, and continuous drug treatment;
• • A history of arterial or venous thromboembolic events within 6 months before enrollment, including myocardial infarction, unstable angina pectoris, cerebrovascular accident or transient ischemic attack, pulmonary embolism, deep vein thrombosis or any other serious thromboembolic events. Thrombosis derived from implantable venous infusion ports or catheters, or superficial venous thrombosis, is excluded if the thrombus is stable after conventional anticoagulant therapy. Prophylactic use of small doses of low-molecular-weight heparin (such as enoxaparin 40 mg/ day) is permitted;
• • Severe bleeding tendency or coagulation dysfunction, or currently undergoing thrombolytic therapy;
• • Uncontrollable hypertension, with a systolic blood pressure greater than 160 mmHg or a diastolic blood pressure greater than 100 after the best medical treatment mmHg, history of hypertensive crisis or hypertensive encephalopathy;
• • Symptomatic congestive heart failure (New York Heart Association Classification II-IV). Symptomatic or poorly controlled arrhythmias. A history of congenital long QT syndrome or corrected QTc\>500 ms during screening;
• • Pulmonary diseases such as a history of pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, drug-related pneumonia, and severe impairment of lung function;
• • Active pulmonary tuberculosis (TB), those who are currently undergoing anti-tuberculosis treatment or have received anti-tuberculosis treatment within one year prior to the first administration of medication; Active hepatitis B and C virus carriers, human immunodeficiency virus carriers, and known syphilis carriers;
• • There was a severe infection in the active stage or with poor clinical control within 4 weeks before enrollment, including but not limited to hospitalization due to infection, bacteremia or severe pneumonia complications;
• * Complications of diabetes, such as:
• • 1. Ketoacidosis
• • 2. Renal insufficiency (urine protein ≥2+, eGFR\<60mL/min/1.73m2);
• • 3. Active or untreated proliferative retinopathy;
• • 4. Diabetic foot ulcer
• • 5. Amputation caused by diabetes;
• • 6. Severe peripheral neuropathy.
• • Have received any non-insulin hypoglycemic drugs or drugs that affect glucose metabolism within 4 weeks or 5 half-lives (of the drug) before enrollment, whichever is shorter.
• • Two or more severe and unexplained hypoglycemic events occurred within 6 months before enrollment;
• • A history of inability to complete the mixed meal tolerance test (MMTT), or a significant allergic reaction (such as anaphylactic shock) to any component in the mixed meal of the MMTT test;
• • Received treatment from other clinical studies within 4 weeks before enrollment;
• • Those who have received attenuated live vaccines within 4 weeks before enrollment;
• • Those who have used any gene therapy products in the past;
• • It is known to be allergic to any component of CNK-UT009 cell injection;
• • Suffering from a known mental illness or substance abuse disorder, and these disorders may interfere with the subject's ability to cooperate with the research requirements;
• • Subjects whose researchers consider to have other life-threatening serious complications that may potentially or interfere with the assessment of this study;
• • Other circumstances that the researcher deems inappropriate to participate in the study.