This is an Early Exploratory Study to Assess the Tolerability and Safety of GC012F in Patients With Multiple Sclerosis

This is a single-arm, open-label, early exploratory clinical study to evaluate the safety and efficacy of GC012F Injection with or without Lymphocyte Depletion (LD) pretreatment in patients with MS, as well as to assess its PK and PD profiles.

This study consists of the following periods: screening period, apheresis day, baseline period(if applicable), lymphodepletion preconditioning period, GC012F infusion, safety and efficacy follow-up period, and long-term follow-up period.

This study consists of three phases: Stage A (Lymphocyte Depletion group ),stage B(Without (Lymphocyte Depletion group) and stage C (expansion period):

Stage A (Lymphocyte Depletion group ):Three evaluable participants were enrolled and received a single dose CAR-T cell infusion, in combination with a Lymphocyte Depletion pre-treatment regimen, in order to establish the initial safety profile of this treatment.

Stage B(Without Lymphocyte Depletion group) :Three evaluable participants were enrolled and received a single dose CAR-T cell infusion,in combination without a Lymphocyte Depletion pre-treatment regimen,To assess the necessity of combining Lymphocyte Depletion pre--treatment.

stage C (expansion period):Enrolled up to 3 evaluable participants and received a single dose CAR-T cell infusion,According to the data of the early stage, consider whether to combine with Lymphocyte Depletion and pre-treatment.

After the administration of GC012F, participants will be followed up for 3 years in this study, and then enter the long-term follow-up period to continue the long-term safety assessment and the persistence assessment of clinical response. The total follow-up period from the administration of GC012F is approximately 15 years.

Inclusion criteria

• 1. The laboratory test results at screening must meet the following criteria:

• a)Absolute neutrophil count ≥ 1.0 × 10^9/L (no growth factor is given for supportive care within 7 days prior to testing);
• b)Absolute lymphocyte count ≥0.5×10^9/L;
• c)Hemoglobin ≥ 80 g/L (no red blood cell transfusion is given within 7 days prior to testing);
• d)Platelet count ≥ 50×10^9/L (no blood transfusion is given within 7 days prior to testing);
• e)Serum IgG ≥ 500 mg/dL;
• f)Activated partial thromboplastin time ≤ 1.5 × upper limit of normal (ULN), prothrombin time (PT) ≤ 1.5 × ULN;
• g)Adequate renal, hepatic, cardiopulmonary function : i.Serum alanine aminotransferase and aspartate aminotransferase ≤ 3 × ULN; ii.Total bilirubin < 2 × ULN (direct bilirubin ≤ 1.5 × ULN for subjects with Gilbert's syndrome); iii.Trial participants with left ventricular ejection fraction ≥ 45% (performed within 8 weeks prior to apheresis) as diagnosed by echocardiography (ECHO) or multi-gated acquisition scan and no evidence of pericardial effusion as determined by ECHO and no clinically significant electrocardiographic findings; iv.Oxygen saturation > 92% under indoor air conditions; v.Estimated glomerular filtration rate ≥ 60 mL/min/1.73 m^2.(CKD-EPI 2021 Formula).
• 2.Confirmed diagnosis of MS based on the 2024 McDonald diagnostic criteria and diagnosis of relapsing or progressive MS based on the 2013 Lublin phenotype criteria for multiple sclerosis;

• Relapsing-remitting multiple sclerosis (RRMS):

• patients with RRMS who have failed ≥ 1 highly effective disease modifying therapy (DMT) (fingolimod, siponimod, ozanimod, and anti-leukocyte cluster of differentiation [CD] 20 monoclonal antibody therapy, etc.) (defined as at least 12 months of continuous use).
• At least 2 clinical relapses in the past 2 years, or 1 clinical relapse in the past 2 years with ≥ 1 new Gd-enhancing lesion on MRI, or ≥ 1 new Gd-enhancing lesion on MRI within the past 6 months; c) ≥ 2 Gd-enhancing lesions on T1-weighted brain MRI at screening.
• Primary progressive multiple sclerosis (PPMS):

• patients with primary progressive MS who have failed highly effective DMT and whose disease activity has worsened recently (i.e., within 1 year) (EDSS disease progression score ≥ 0.5);
• no Gd-enhancing lesions on brain MRI at screening.
• Secondary progressive multiple sclerosis (SPMS):

• patients with secondary progressive MS who have failed highly effective DMT and whose disease activity has worsened recently (i.e., within 1 year) (EDSS disease progression score ≥ 0.5);
• no Gd-enhancing lesions on brain MRI at screening.
• 3.EDSS score ≥ 2.0 and ≤ 6.5;
• 4.Documented history or confirmation at screening of the presence of oligoclonal bands or an elevated IgG index or the KFLC index in CSF.

Exclusion criteria

• 1.Fungal, bacterial, viral, or other infection not controlled and/or requiring hospitalization or intravenous antimicrobial therapy within 4 weeks prior to screening. Uncomplicated urinary tract infection and uncomplicated bacterial pharyngitis are permitted if responding to current therapy;
• 2.Active tuberculosis or latent tuberculosis that has not been treated appropriately prior to screening;
• 3.History of severe hypersensitivity or allergy;
• 4.Primary immunodeficiency;
• 5.Impaired cardiac function or clinically significant cardiac disease;
• 6.History of serious respiratory diseases or current serious respiratory diseases, including moderate or severe or above asthma or chronic obstructive pulmonary disease, interstitial lung disease, or pulmonary fibrosis;
• 7.Current or history of cirrhosis;
• 8.History of Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus within the past 2 years, and the need for continuous use of systemic immunosuppressants/systemic disease-modifying drugs;
• 9.Any active malignancy or history of malignancy within 5 years prior to screening. The following are exceptions: early-stage tumors that have undergone radical treatment (carcinoma in situ or stage I tumors, non-ulcerative primary melanoma with a depth < 1 mm and no lymph node involvement), basal cell carcinoma of the skin, squamous cell carcinoma of the skin, thyroid carcinoma in situ or early-stage thyroid cancer that has undergone radical treatment, cervical carcinoma in situ, or breast cancer in situ that has undergone potentially radical treatment;
• 10.Those who have clinically significant bleeding symptoms or definite haemorrhagic diathesis within 6 months prior to screening;
• 11.Arterial or venous thrombotic events such as cerebrovascular disorders (including cerebral hemorrhage, cerebral infarction, etc), deep venous thrombosis, and/or pulmonary embolism within 6 months prior to screening;
• 12.Hematologic disorders: History of cytopenia consistent with myelodysplastic syndrome; history of sickle-cell anemia or other hemoglobinopathies;
• 13.Severe underlying medical conditions, such as:

• Significant clinical evidence of dementia or mental status changes;
• History of any other central nervous system (CNS) disorders or neurodegenerative diseases, such as epilepsy, seizure, paralysis, aphasia, stroke, severe brain injury, dementia, Parkinson's disease, and psychosis;
• Mental disorders or psychosocial conditions that place patients at unacceptable risk.
• 14.Positive results in any of the following tests:

• Positive for human immunodeficiency virus (HIV) antibody;
• Positive for hepatitis B surface antigen (HBsAg); or positive for hepatitis B core antibody (HBcAb) with hepatitis B virus deoxyribonucleic acid (DNA) above the lower limit of detection of the assay;
• Positive for hepatitis C virus (HCV) antibody with HCV ribonucleic acid (RNA) above the lower limit of detection of the assay;
• Positive for antibodies against human T-cell lymphotropic virus types I and II;
• Positive for syphilis antibody. As the immunosuppression included in this study may pose an unacceptable risk, those with active HIV infection, hepatitis B (positive for HBsAg), or HCV infection (positive for anti-HCV antibodies) are excluded. Subjects are allowed to have a previous history of hepatitis B or C, provided that viral load is shown to be below the limit of detection by quantitative polymerase chain reaction and/or nucleic acid testing. Hepatitis B surface antibodies produced following hepatitis B vaccination are not considered evidence of prior infection.
• 15.Administration of a live attenuated vaccine within 4 weeks prior to apheresis;
• 16.Receipt of a different investigational drug in a clinical trial within 4 weeks prior to apheresis, or the time interval from the last dose of the investigational drug in the previous drug clinical trial to the informed consent form (ICF) signing date is still within 5 half-lives of that drug (whichever is longer);
• 17.Splenectomy within 12 months prior to the signing of ICF;
• 18.Prior therapy targeting CD19 and/or BCMA, or CAR T product therapy against any target;
• 19.Within 4 weeks prior to the apheresis, the trial participants had received treatment with targeted B-cell therapies, including but not limited to rituximab, ofatumumab, or orelizumab;
• 20.Patients treated with siponimod and ozanimod within 1 month prior to apheresis;
• 21.Patients treated with fingolimod within 6 weeks prior to apheresis;
• 22.Patients treated with teriflunomide within 3 months prior to apheresis;
• 23.Patients treated with dimethyl fumarate therapy within 2 weeks prior to apheresis;
• 24.Major surgery within 8 weeks before the signing of ICF or planned surgery during the study (except for subjects scheduled for surgery under local anesthesia, provided that the surgery will not be performed within 2 weeks after infusion);
• 25.Previous history of organ transplantation;
• 26.History of neuromyelitis optica spectrum disorder or myelin oligodendrocyte glycoprotein antibody-related disease, or neurological diseases suspected of MS at screening;
• 27.History of CNS or spinal cord tumors, metabolic or infectious spinal cord lesions, hereditary progressive CNS diseases, sarcoidosis, or non-MS progressive neurological diseases that interfere with study assessments;
• 28.CNS disorders, such as cerebrovascular ischemia/hemorrhage, dementia, previous or current spinal cord lesions, cerebellar diseases unrelated to MS, or other diseases deemed by the investigator to potentially interfere with neurotoxicity assessment;
• 29.History of seizures, even if seizures have been well controlled with antiepileptic drugs;
• 30.MS lesions or symptoms that have the potential to increase the risk of neurotoxicity, including but not limited to tumor-like lesions (≥ 3 cm in diameter within 5 years prior to screening) or depressed level of consciousness, and/or the presence of active, clinically significant concomitant CNS pathological changes other than MS, which may impact interpretation of study results or complicate identification or assessment of neurotoxicity;
• 31. Any contraindications to lumbar puncture (LP), including but not limited to:

• Known or suspected structural abnormalities of the lumbar vertebra that, in the opinion of the investigator, may interfere with the conduct of LP or increase the risk of the procedure to the trial participant ;
• Risk of increased or uncontrollable bleeding, including but not limited to vascular abnormalities or tumors at or around the LP site, coagulation cascade disorders, abnormal platelet function, or abnormal platelet counts;
• Trial participants who are taking an anticoagulant (e.g., warfarin) or an antiplatelet agent (low-dose aspirin [100 mg/day or less] is permitted) do not meet the inclusion criteria unless the investigator considers it safe for the patient to temporarily discontinue the anticoagulant or antiplatelet therapy for LP;
• 32.Trial participants who are unwilling or unable to undergo MRI per protocol requirements, such as those who are unable to undergo MRI due to claustrophobia, or those with clear contraindications to MRI (e.g., metal implants, metal foreign bodies in the body, cardiac pacemakers, defibrillators, etc.);
• 33.Circumstances that, as judged by the investigator, may hinder the subject's full participation in the study or confuse the study results, or render participation in this study not in the trial participant's best interests.
• 34.Based on the Columbia-Suicidality Severity Rating Scale (C-SSRS), participants have current suicidal intent, i.e., "yes" to question 4 (active suicidal ideation with intent to act but no specific plan) or question 5 (active suicidal ideation with specific plan and intent) on the C-SSRS or have a current history of suicidal behavior。