Key Inclusion criteria:
1. All subjects or legal guardians must sign an ethics committee-approved informed consent form in writing prior to initiation of any screening procedures.
2. Male or female subject over 18 years old and under 70 years old at the time of evaluation; Weight ≥ 40 kg.
3. Diagnosed with inflammatory bowel disease assessed by the investigator and the disease course has been ≥ 3 months before signing informed consent (clinical manifestations, endoscopy and histopathological reports consistent with the diagnosis of inflammatory bowel disease are required).
4. The subject has documented inadequate response, loss of response, or intolerance to at least one advanced therapy for IBD.
5. Patients with IBD during the screening period need to meet the requirements of moderate to severe IBD; UC: active ulcerative colitis, defined as per the adapted Mayo score criteria. CD: CD subjects with moderate to severe active CD, defined as interpreted by SES-CD.
6. Life expectancy greater than 6 months;
7. Female individuals with fertility (defined as all females who are physiologically capable of becoming pregnant) must provide informed consent, have a negative blood pregnancy test result, and agree to use highly effective contraception from the time of informed consent until 1 year after CAR-T cell infusion. Male individuals with fertility must agree to use effective barrier contraception from the time of informed consent until 1 year after CAR-T cell infusion, and should not donate semen or sperm during the entire study period.
8. Indeterminate colitis is permitted.
Key Exclusion criteria:
1. Subjects who have previously received any BCMA and/or CD19 targeted cell therapy products or CAR-T therapy for any target before signing the informed consent form.
2. Undiagnosed type colitis, fulminant colitis, Hirschsprung-associated enterocolitis (HAEC), microscopic colitis, ischemic colitis, radiation colitis, colitis-related diverticular disease, or other colitis or enteritis type that may confound the evaluation of efficacy.
3. Subjects with malignant tumors or dysplasia on endoscopy.
4. Subjects with severely impaired vital organ function.
5. Impaired bone marrow function.
6. Active hepatitis B, HCV positive, HIV antibody positive, Treponema pallidum antibody positive, Active tuberculosis.
7. Presence of any IBD related complications determined by the investigator to interfere with the study of ICG318 CAR-T in refractory IBD.
8. History of bleeding within 30 days determined by the investigator to exclude the patient.
9. Infectious diseases: subjects with acute, life-threatening bacterial, viral or fungal infections that have not been controlled.
10. Hospitalization for IBD-related complications within 30 days prior to screening.
11） Clinically significant central nervous system disease determined by the investigator to impair the subjects ability to participate safely in this trial.
12） Subjects with prior or concurrent malignancies. Exceptions may be determined at the discretion of the investigator.
13） Vaccination within 30 days before screening and vaccination within 3 months after planned cell ICG318 CAR-T infusion.
14） Subjects who are receiving or have received another investigational drug or drugs without adequate washout time as determined by the principal investigator.
15） Those who are judged by the investigator to be unfit for leukapheresis, or whose IBD disease severity and trajectory are not compatible with infusion with ICG318 CAR-T cells, or any critical steps of the trial evaluation such as but not limited to contraindications to colonoscopy.
16） Female subjects who are pregnant or lactating. 17） Autoimmune diseases judged by the investigator to require systemic treatment and affect the evaluation of efficacy.
18） Suicidal tendencies, tobacco use, substance use, or alcohol abuse as determined by the investigator.
19） Those who have a history of a severe drug allergy, or are allergic to the test drug ingredients, excipients or combined therapeutic drugs.
20） Other conditions that the investigator believes should not participate in this clinical trial.
