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A Study of IMS001 in Patients With Multiple Sclerosis
A Clinical Study of IMS001 Injection (Human Embryonic Stem Cell-Derived Mesenchymal-Like Stem Cells) for the Treatment of Multiple Sclerosis
This study will evaluate the safety and tolerability of IMS001 and explore its possible effects in adults with multiple sclerosis. IMS001 is an investigational cell therapy consisting of mesenchymal-like stem cells derived from human embryonic stem cells.
The study plans to enroll 4 adults aged 18 to 65 years with relapsing-remitting or secondary progressive multiple sclerosis in China. Each participant will receive a single infusion of IMS001 into a vein. All participants will receive IMS001, and both participants and the study team will know which treatment is given.
Participants will undergo screening for up to 4 weeks before treatment. After the infusion, they will be assessed over 12 months for side effects and changes in multiple sclerosis, including relapses, disability, brain magnetic resonance imaging (MRI) findings, vision, movement, and thinking abilities.
Participants will then enter an additional 24-month follow-up period to monitor long-term safety, including serious side effects and possible tumor development. Total participation may last up to 37 months, including screening.
Studie Overzicht
Studietype
Inschrijving (Geschat)
Fase
- Fase 1
Contacten en locaties
Studie Locaties
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Sichuan
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Chengdu, Sichuan, China
- Werving
- West China Hospital, Sichuan University
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Contact:
- Anjiao Peng
- Telefoonnummer: +86 18382093738
- E-mail: pengneurology@163.com
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
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Voluntarily provides written informed consent.
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Aged 18 to 65 years, inclusive, of either sex.
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Has relapsing-remitting multiple sclerosis (RRMS) or secondary progressive multiple sclerosis (SPMS), diagnosed according to the 2017 McDonald criteria.
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Has an Expanded Disability Status Scale (EDSS) score of 3.0 to 7.5, inclusive.
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Has experienced at least one of the following despite disease-modifying therapy (DMT):
- One relapse within the year before screening, or at least two relapses within the two years before screening.
- Confirmed disability progression, as assessed by the investigator.
- Gadolinium-enhancing T1 lesions and/or new or enlarging T2 lesions on magnetic resonance imaging (MRI).
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Has had no clinical relapse within one month before screening.
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Has had multiple sclerosis for more than one year.
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Women of childbearing potential must agree to use effective contraception during the study and for six months after the last dose of study treatment, and must have negative pregnancy tests at screening and baseline.
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Male participants with partners of childbearing potential must agree to use effective contraception for three months after the last dose of study treatment and must not donate sperm during this period.
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Is able and willing to undergo gadolinium administration and repeated MRI examinations.
Exclusion Criteria:
- Known or suspected allergy to human serum albumin, diphenhydramine, acetaminophen, methylprednisolone, or any component of IMS001.
- Use of teriflunomide within 12 months before screening, unless an 11-day elimination procedure using cholestyramine or another appropriate elimination agent has been completed.
- Use of alemtuzumab within 12 months before screening, or cladribine, rituximab, ocrelizumab, or another anti-CD20 monoclonal antibody within six months before screening.
- Use of ofatumumab, natalizumab, or ozanimod, or treatment with plasma exchange, within three months before screening.
- Use of mitoxantrone, cyclophosphamide, azathioprine, methotrexate, cyclosporine, mycophenolate mofetil, fingolimod, siponimod, ponesimod, or systemic corticosteroids within one month before screening.
- Use of interferon beta-1a/1b, glatiramer acetate, dimethyl fumarate, diroximel fumarate, or monomethyl fumarate within two weeks before screening. Generic equivalents of glatiramer acetate and dimethyl fumarate are included.
- Previous treatment with any allogeneic cell therapy or tissue transplantation.
- History of a neoplastic disease, except basal cell carcinoma; nonmetastatic cutaneous squamous cell carcinoma excised with clear margins; adequately treated cervical carcinoma in situ; or low-risk differentiated papillary thyroid carcinoma or noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) that has been definitively treated, without recurrence, and meets the required disease-free survival criteria.
- Clinically significant electrocardiogram abnormalities during screening.
- Known or documented HIV or syphilis infection, or active hepatitis B or hepatitis C infection.
- Abnormal liver function, including total bilirubin greater than 2 times the upper limit of normal (ULN), except isolated Gilbert syndrome, or AST or ALT greater than 3 times ULN.
- White blood cell count below 3 × 10^9/L; lymphocyte count below 0.8 × 10^9/L; hemoglobin below 90 g/L; or platelet count below 80 × 10^9/L.
- Estimated glomerular filtration rate below 30 mL/min/1.73 m² during screening, calculated using the 2021 CKD-EPI equation; acute kidney injury; need for renal replacement therapy; or another clinically significant active or unstable kidney disease, as judged by the investigator.
- History of another autoimmune disease, myelodysplasia, or a hematological disease.
- Pregnancy, breastfeeding, or plans to become pregnant during the study.
- Inability to receive study treatment during the trial, likely noncompliance with the protocol, or any other circumstance considered unsuitable by the investigator.
- Participation in another clinical trial of a drug or device within three months before enrollment.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: IMS001 Treatment
All 4 participants will receive a single intravenous infusion of IMS001 at the same dose level. |
IMS001 is a human embryonic stem cell-derived mesenchymal-like stem cell product. Each participant will receive a single intravenous infusion at a dose of 1 × 10^6 cells/kg on Day 1. |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Number of Participants With IMS001-Related Adverse Events
Tijdsspanne: From IMS001 infusion on Day 1 through Month 12
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Number of participants who experience at least one adverse event assessed by the investigator as related to IMS001. Events will be summarized by type, severity, seriousness, and relationship to treatment. |
From IMS001 infusion on Day 1 through Month 12
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Medewerkers en onderzoekers
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Ziekten van het zenuwstelsel
- Pathologische processen
- Chronische ziekte
- Ziekte attributen
- Auto-immuunziekten
- Ziekten van het immuunsysteem
- Demyeliniserende auto-immuunziekten, CZS
- Auto-immuunziekten van het zenuwstelsel
- Demyeliniserende ziekten
- Pathologische aandoeningen, tekenen en symptomen
- Multiple sclerose
- Multiple sclerose, relapsing-remitting
- Multiple sclerose, chronisch progressief
Andere studie-ID-nummers
- IMS001-01
- ChiCTR2600129418 (Register-ID: Chinese Clinical Trial Registry (ChiCTR))
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .