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Safety and Efficacy of S103 Cells in Progressive/Refractory Multiple Sclerosis (RESET-MS)

7. Mai 2026 aktualisiert von: 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.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

9

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

    • Shaanxi
      • Xi'an, Shaanxi, China, 710032
        • Xijing Hospital
        • Kontakt:
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  1. Age ≥18 years and ≤75 years;
  2. 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;
  3. 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);
  4. 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;
  5. 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;
  6. 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:

  1. 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;
  2. 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;
  3. 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;
  4. 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;
  5. 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;
  6. 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;
  7. 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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Sequenzielle Zuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: S103 cells
subjects will undergo leukapheresis followed by lymphodepletion conditioning with cyclophosphamide and fludarabine, then receive S103 CAR-T cell infusion.
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

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence and type of Dose-Limiting Toxicities (DLTs)
Zeitfenster: From Day 1 up to Day 28 post S103 infusion
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.
From Day 1 up to Day 28 post S103 infusion
Incidence and severity of AEs, including changes in vital signs, physical examination, laboratory parameters, Electrocardiograms and Echocardiograms.
Zeitfenster: From Day 1 up to week 26 post S103 infusion
To evaluate the AEs occurring within 6 months after S103 infusion
From Day 1 up to week 26 post S103 infusion

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
PD-soluble BCMA
Zeitfenster: From Day 1 up to week 26 post S103 infusion
The changes in concentration of BCMA in the peripheral blood after S103 infusion
From Day 1 up to week 26 post S103 infusion
PK-BCMA CAR-T cells
Zeitfenster: From Day 1 up to Day 28 post S103 infusion
The concentration of BCMA-CAR T cells(cells/mL) in peripheral blood after administration was detected by flow cytometry
From Day 1 up to Day 28 post S103 infusion
PD-NFL
Zeitfenster: From Day 1 up to week 26 post S103 infusion
The changes in peripheral blood neurofilament light chain(NfL) concentration in patients with MS
From Day 1 up to week 26 post S103 infusion
PD-OB
Zeitfenster: From Day 1 up to week 26 post S103 infusion
The changes in CSF Oligoclonal Bands index in patients with MS
From Day 1 up to week 26 post S103 infusion
Changes of Expanded Disability Status Scale(EDSS)scores
Zeitfenster: From Day 1 up to week 26 post S103 infusion
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.
From Day 1 up to week 26 post S103 infusion

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Changes in proportion of peripheral blood immune cell subsets and inflammatory markers levels
Zeitfenster: From Day 1 up to week 26 post S103 infusion
Changes in proportion of peripheral blood immune cell subsets and inflammatory markers levels of subjects after infusion of S103
From Day 1 up to week 26 post S103 infusion
Changes in Cerebrospinal Fluid (CSF) parameters
Zeitfenster: From Day 1 up to week 26 post S103 infusion
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
From Day 1 up to week 26 post S103 infusion
MS: Annualized Relapse Rate (ARR)
Zeitfenster: From Day 1 up to 1 year post S103 infusion
Annualized relapse rate (ARR): Number of MS relapses divided by person-years of observation
From Day 1 up to 1 year post S103 infusion
Time to first relapse
Zeitfenster: From Day 1 up to 1 year post S103 infusion
Time from S103 infusion to the first relapse of MS
From Day 1 up to 1 year post S103 infusion
Imaging prognostic evaluation
Zeitfenster: At baseline (pre-infusion), Day 28, and week 26 post S103 infusion
Neurological imaging assessments before intervention and at 26 weeks after intervention, including: gadolinium-enhancing lesions, T2, SWI, and other relevant MRI sequences.
At baseline (pre-infusion), Day 28, and week 26 post S103 infusion
Percent of NEDA-3
Zeitfenster: From Day 1 up to 1 year post S103 infusion
The proportion of patients achieving no evidence of disease activity-3 (NEDA-3), defined as no relapse, no disability worsening, and no MRI activity
From Day 1 up to 1 year post S103 infusion
9-Hole Peg Test (9-HPT)
Zeitfenster: At baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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.
At baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
Change in Timed 25-Foot Walk (T25-FW) Time
Zeitfenster: At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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.
At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
Change in Mini-Mental State Examination (MMSE) Score
Zeitfenster: At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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.
At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
Change in Montreal Cognitive Assessment (MoCA) Score
Zeitfenster: At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion
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.
At Baseline (pre-infusion), Month 1, Month 3, and Month 6 post S103 infusion

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Mai 2026

Primärer Abschluss (Geschätzt)

1. November 2027

Studienabschluss (Geschätzt)

1. November 2029

Studienanmeldedaten

Zuerst eingereicht

28. April 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

7. Mai 2026

Zuerst gepostet (Tatsächlich)

14. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

14. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

7. Mai 2026

Zuletzt verifiziert

1. April 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

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UNENTSCHIEDEN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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