- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07587125
Safety and Efficacy of S103 Cells in Progressive/Refractory Multiple Sclerosis (RESET-MS)
7 maggio 2026 aggiornato da: Xijing Hospital
Safety and Efficacy of S103 Cells in Patients With Progressive or Refractory Multiple Sclerosis:An Open-Label, Single-Arm, Exploratory Clinical Study
This study is a single-center, open-label, single-arm, exploratory clinical study to evaluate the safety, tolerability, and preliminary efficacy of S103(BCMA-CAR T )cells in the treatment of progressive or refractory multiple sclerosis.
The study is a dose escalation trial in adult progressive and refractory MS patients.
A standard "3+3" design will be used to perform dose escalation to explore the safety profile and dose-limiting toxicities (DLTs).
A total of 9 MS patients who meet the inclusion criteria are expected to be recruited.
Panoramica dello studio
Stato
Non ancora reclutamento
Condizioni
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Stimato)
9
Fase
- Fase 1
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Wen Jiang Dr.
- Numero di telefono: 86 29 84771319
- Email: jiangwen@fmmu.edu.cn
Backup dei contatti dello studio
- Nome: Xiaodan Shi Dr.
- Numero di telefono: +86 29 84771319
- Email: Shixd999@163.com
Luoghi di studio
-
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Shaanxi
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Xi'an, Shaanxi, Cina, 710032
- Xijing Hospital
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Contatto:
- Wen Jiang, Dr.
- Numero di telefono: +86 29 84771319
- Email: jiangwen@fmmu.edu.cn
-
Contatto:
- Xiaodan Shi, Dr.
- Numero di telefono: +86 29 84771319
- Email: Shixd999@163.com
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
Inclusion Criteria:
- Age ≥18 years and ≤75 years;
- The subject signs the informed consent form, is willing and able to comply with the protocol, complete the research assessments and return for follow-up;
- To be diagnosed with Multiple Sclerosis (MS) according to the 2017 McDonald criteria, specifically including Progressive MS (Primary Progressive MS [PPMS] or Secondary Progressive MS [SPMS]) or Relapsing-Remitting MS (RRMS);
- The subject must be assessed by the investigator as having progressive or refractory MS for which no effective standard therapy is available. For subjects with Relapsing MS (RMS), refractory/progressive disease is defined as having experienced at least 2 clinical relapses within the past 2 years, or at least 1 clinical relapse within the past 1 year accompanied by at least one gadolinium-enhancing lesion on MRI within the past year, despite treatment with standard disease-modifying therapies (DMTs). In addition, the subject must have an Expanded Disability Status Scale (EDSS) score between 2.0 and 7.0, inclusive, at both screening and baseline;
- Male study participants must agree to take contraceptive measures during the treatment period and within 1 year after receiving study treatment, and are prohibited from donating sperm throughout the study period;
- Women of childbearing potential (WOCBP) must agree to take contraceptive measures during treatment and for at least 1 year after receiving study treatment. Participants must have a negative serum pregnancy test result during screening; a negative urine pregnancy test result must be confirmed before receiving CAR-T for the first time.
Exclusion Criteria:
Subjects will be ineligible for inclusion in the study if they meet any of the following criteria prior to screening or at the baseline visit:
- The subject has any medical, psychological, or social condition that, in the investigator's opinion, may harm the subject, interfere with their ability to participate in the study, or result in poor protocol compliance;
- Female subjects who are pregnant or lactating, plans to become pregnant at any time within 12 months after receiving CAR-T cell treatment, or has a history of spontaneous or induced abortion within 4 weeks prior to screening;
- The subject has a clinically relevant active infection, such as sepsis, pneumonia, or a severe local abscess, or a serious infection requiring hospitalization or intravenous antibiotic treatment within 4 weeks prior to screening. Subjects are also excluded if they have a known immunodeficiency disorder including Human Immunodeficiency Virus (HIV), test positive for Hepatitis B surface antigen (HBsAg) or detectable Hepatitis B virus (HBV) DNA, test positive for Hepatitis C virus (HCV) antibody with detectable HCV RNA, test positive for syphilis during the screening period, or have an active or high-risk history of tuberculosis infection;
- The subject has previously received any Chimeric Antigen Receptor (CAR) T-cell therapy or other genetically modified cell therapies, or has a history of allogeneic hematopoietic stem cell transplantation (HSCT) or solid organ transplantation. Furthermore, subjects are excluded if they have received intravenous immunoglobulin (IVIG) or plasma exchange (PE) within 4 weeks prior to screening, or have received tocilizumab or eculizumab treatment within 3 months prior to screening;
- The subject is diagnosed with an active, severe autoimmune disease other than Multiple Sclerosis, such as Systemic Lupus Erythematosus or Rheumatoid Arthritis. This also includes the presence of other severe progressive neurodegenerative or central nervous system (CNS) disorders, such as Parkinson's disease, Alzheimer's disease, stroke, or active CNS tumors, that the investigator believes would confound the clinical assessment of Multiple Sclerosis. Additionally, a history of active malignancy within the past 5 years excludes the subject, with the exception of adequately treated basal cell or squamous cell carcinoma of the skin, or carcinoma in situ of the cervix;
- The subject exhibits specific laboratory abnormalities or organ dysfunction during the screening period, including elevated liver enzymes with AST or ALT greater than 1.5 times the upper limit of normal (ULN), total bilirubin greater than 1.5 times the ULN, or a Creatinine Clearance (CrCl) of less than 60 mL/min. Exclusions also apply for an absolute neutrophil count (ANC) of less than 2.0 × 10^9/L, a platelet count of less than 100 × 10^9/L, hemoglobin levels below 100 g/L, or severe cardiovascular or pulmonary diseases, which include a Left Ventricular Ejection Fraction (LVEF) below 50%, unstable angina or myocardial infarction within the past 6 months, or a resting peripheral blood oxygen saturation (SpO2) of 91% or less;
- The subject has a known severe allergy, hypersensitivity, or intolerance to fludarabine, cyclophosphamide, or any excipients contained in the S103 CAR-T cell product, such as human serum albumin. Subjects are also excluded if they have received any live attenuated vaccine within 6 weeks prior to screening, or plan to receive a live vaccine during the study period.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione sequenziale
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: S103 cells
subjects will undergo leukapheresis followed by lymphodepletion conditioning with cyclophosphamide and fludarabine, then receive S103 CAR-T cell infusion.
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Dose Level 0 (De-escalation dose): 0.5×10^6 CAR-T cells/kg Dose Level 1 (Starting dose): 1.0×10^6 CAR-T cells/kg Dose Level 2 (Maximum dose): 2.0×10^6 CAR-T cells/kg
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Incidence and type of Dose-Limiting Toxicities (DLTs)
Lasso di tempo: From Day 1 up to Day 28 post S103 infusion
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A DLTs is defined as any Grade 4 toxicity or Grade 3 toxicity lasting more than 7 days occurring within 28 days after BCMA-CAR T infusion that is related to the treatment (with specific exceptions for manageable CRS, neurotoxicity, and hematologic toxicities as defined in the protocol).
This is used to determine the safety and tolerable dose.
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From Day 1 up to Day 28 post S103 infusion
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Incidence and severity of AEs, including changes in vital signs, physical examination, laboratory parameters, Electrocardiograms and Echocardiograms.
Lasso di tempo: From Day 1 up to week 26 post S103 infusion
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To evaluate the AEs occurring within 6 months after S103 infusion
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From Day 1 up to week 26 post S103 infusion
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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PD-soluble BCMA
Lasso di tempo: From Day 1 up to week 26 post S103 infusion
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The changes in concentration of BCMA in the peripheral blood after S103 infusion
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From Day 1 up to week 26 post S103 infusion
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PK-BCMA CAR-T cells
Lasso di tempo: From Day 1 up to Day 28 post S103 infusion
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The concentration of BCMA-CAR T cells(cells/mL) in peripheral blood after administration was detected by flow cytometry
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From Day 1 up to Day 28 post S103 infusion
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PD-NFL
Lasso di tempo: From Day 1 up to week 26 post S103 infusion
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The changes in peripheral blood neurofilament light chain(NfL) concentration in patients with MS
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From Day 1 up to week 26 post S103 infusion
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PD-OB
Lasso di tempo: From Day 1 up to week 26 post S103 infusion
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The changes in CSF Oligoclonal Bands index in patients with MS
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From Day 1 up to week 26 post S103 infusion
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Changes of Expanded Disability Status Scale(EDSS)scores
Lasso di tempo: From Day 1 up to week 26 post S103 infusion
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The EDSS score ranges from 0 to 10, with higher scores indicating worse disability.
A negative change relative to baseline indicates clinical improvement.
Disability worsening is defined as follows: an increase of at least 2.0 points if the baseline EDSS score is 0; an increase of at least 1.0 point if the baseline EDSS score is 1.0 to 5.0; and an increase of at least 0.5 points if the baseline EDSS score is 5.5 or higher.
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From Day 1 up to week 26 post S103 infusion
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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Changes in proportion of peripheral blood immune cell subsets and inflammatory markers levels
Lasso di tempo: From Day 1 up to week 26 post S103 infusion
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Changes in proportion of peripheral blood immune cell subsets and inflammatory markers levels of subjects after infusion of S103
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From Day 1 up to week 26 post S103 infusion
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Changes in Cerebrospinal Fluid (CSF) parameters
Lasso di tempo: From Day 1 up to week 26 post S103 infusion
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Evaluation of central nervous system (CNS) microenvironment changes through lumbar puncture.
Parameters include CSF cytology, biochemistry, cytokines, lymphocyte subsets, free kappa light chains, and oligoclonal band (OB) index, and multi-omics analysis of cerebrospinal fluid immune microenvironment
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From Day 1 up to week 26 post S103 infusion
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MS: Annualized Relapse Rate (ARR)
Lasso di tempo: From Day 1 up to 1 year post S103 infusion
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Annualized relapse rate (ARR): Number of MS relapses divided by person-years of observation
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From Day 1 up to 1 year post S103 infusion
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Time to first relapse
Lasso di tempo: From Day 1 up to 1 year post S103 infusion
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Time from S103 infusion to the first relapse of MS
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From Day 1 up to 1 year post S103 infusion
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Imaging prognostic evaluation
Lasso di tempo: At baseline (pre-infusion), Day 28, and week 26 post S103 infusion
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Neurological imaging assessments before intervention and at 26 weeks after intervention, including: gadolinium-enhancing lesions, T2, SWI, and other relevant MRI sequences.
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At baseline (pre-infusion), Day 28, and week 26 post S103 infusion
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Percent of NEDA-3
Lasso di tempo: From Day 1 up to 1 year post S103 infusion
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The proportion of patients achieving no evidence of disease activity-3 (NEDA-3), defined as no relapse, no disability worsening, and no MRI activity
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From Day 1 up to 1 year post S103 infusion
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9-Hole Peg Test (9-HPT)
Lasso di tempo: At baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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Change from baseline in the 9-Hole Peg Test (9-HPT), measured in seconds.
A higher value indicates worse upper extremity function.
A negative change from baseline indicates improvement.
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At baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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Change in Timed 25-Foot Walk (T25-FW) Time
Lasso di tempo: At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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Change from baseline in the Timed 25-Foot Walk (T25-FW), measured in seconds.
A higher value indicates worse ambulatory function.
A negative change from baseline indicates improvement.
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At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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Change in Mini-Mental State Examination (MMSE) Score
Lasso di tempo: At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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Change from baseline in the Mini-Mental State Examination (MMSE) score.
Scores range from 0 to 30, with higher scores indicating better cognitive function.
A positive change from baseline indicates improvement.
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At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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Change in Montreal Cognitive Assessment (MoCA) Score
Lasso di tempo: At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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Change from baseline in the Montreal Cognitive Assessment (MoCA) score.
Scores range from 0 to 30, with higher scores indicating better cognitive function.
A positive change from baseline indicates improvement.
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At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Collaboratori
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
1 maggio 2026
Completamento primario (Stimato)
1 novembre 2027
Completamento dello studio (Stimato)
1 novembre 2029
Date di iscrizione allo studio
Primo inviato
28 aprile 2026
Primo inviato che soddisfa i criteri di controllo qualità
7 maggio 2026
Primo Inserito (Effettivo)
14 maggio 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
14 maggio 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
7 maggio 2026
Ultimo verificato
1 aprile 2026
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie del sistema nervoso
- Processi patologici
- Malattia cronica
- Attributi della malattia
- Malattie autoimmuni
- Malattie del sistema immunitario
- Malattie autoimmuni demielinizzanti, SNC
- Malattie autoimmuni del sistema nervoso
- Malattie demielinizzanti
- Condizioni patologiche, segni e sintomi
- Sclerosi multipla
- Sclerosi Multipla Cronica Progressiva
Altri numeri di identificazione dello studio
- KY20262101JIANGWEN
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
INDECISO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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