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In Vivo BCMA/GPRC5D Tandem Dual CAR-T Therapy for Relapsed/Refractory Plasma Cell Neoplasms

7 mei 2026 bijgewerkt door: Liping Dou

A Clinical Study on the Safety of in Vivo-CAR-T Cell Immunotherapy Targeting BCMA/GPRC5D for the Treatment of Relapsed/Refractory Plasma Cell Neoplasms

This study aims to assess the safety profile of in vivo BCMA/GPRC5D-targeted CAR-T cell immunotherapy in patients with relapsed or refractory plasma cell neoplasms.

Studie Overzicht

Toestand

Nog niet aan het werven

Gedetailleerde beschrijving

This is a single-center, open-label, single-arm, prospective study designed to evaluate the safety of in vivo BCMA/GPRC5D-targeted CAR-T cell immunotherapy in patients with relapsed or refractory plasma cell neoplasms. The study employs a dose-escalation design to assess safety, tolerability, and preliminary efficacy. Safety assessments primarily focus on potential adverse events (AEs) following infusion of SL4903 injection, including the number of cases, incidence rates, and severity of cytokine release syndrome, immune effector cell therapy-related neurotoxicity, hematologic toxicity, organ toxicity, ect. Efficacy assessments will include overall objective response rate (ORR), event-free survival (EFS), overall survival (OS), progression-free survival (PFS), duration of complete remission, relapse rate, and mortality rate. Exploratory analyses will focus on characterizing the in vivo kinetics of CAR-T cells and the clonal evolution of plasma cell neoplasms during and after consolidation treatment.

Studietype

Ingrijpend

Inschrijving (Geschat)

18

Fase

  • Vroege fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Voluntary signing of informed consent by the subject or legally authorized representative, with willingness and ability to comply with scheduled visits, study treatment, laboratory tests, and other study procedures.
  • Diagnosis of relapsed or refractory plasma cell neoplasms meeting the following criteria:

    1. Clonal plasma cells confirmed to be BCMA and/or GPRC5D positive by flow cytometry or immunohistochemistry;
    2. Previously treated with at least 2 lines of anti-plasma cell neoplasms therapy, with at least 1 complete treatment cycle for each line, and evidence of disease progression within 12 months after the most recent anti-plasma cell neoplasms treatment, or being refractory to both immunomodulatory drugs and proteasome inhibitors, with disease progression within 2 months after the most recent anti-plasma cell neoplasms treatment (according to the IMWG diagnostic criteria)
  • Age 18 to 75 years (inclusive), male or female.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
  • Life expectancy > 3 months from the date of informed consent.
  • Hemoglobin (HGB) ≥ 60 g/L (transfusion allowed).
  • Adequate organ function (hepatic, renal, cardiac, and pulmonary):

    1. Creatinine ≤ 2 × ULN;
    2. Left ventricular ejection fraction (LVEF) ≥ 50%;
    3. Oxygen saturation > 90%;
    4. Total bilirubin ≤ 1.5 × ULN; ALT and AST ≤ 2.5 × ULN.
  • Willingness to use highly effective contraception from signing of informed consent until 1 year after SL4903 infusion.

Exclusion Criteria:

  • Severe cardiac dysfunction with left ventricular ejection fraction (LVEF) < 50%.
  • History of severe pulmonary impairment.
  • Concurrent diagnosis of another active malignancy.
  • Uncontrolled active infection.
  • History of severe autoimmune disease or primary immunodeficiency.
  • Active hepatitis (defined as HBV DNA or HCV RNA above the lower limit of detection).
  • Human immunodeficiency virus (HIV) infection or acquired immunodeficiency syndrome (AIDS), or active syphilis.
  • History of severe hypersensitivity to biological products (including antibiotics).
  • Allogeneic hematopoietic stem cell transplant recipients with ongoing acute graft-versus-host disease (GVHD) despite discontinuation of immunosuppressive therapy for at least one month prior to screening.
  • Any other severe comorbidities or laboratory abnormalities that, in the investigator's opinion, would increase the risk to the subject or interfere with study results, rendering the subject unsuitable for participation.
  • Pregnant or breastfeeding women (including women of childbearing potential who are pregnant or lactating).

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

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
Experimenteel: In vivo BCMA/GPRC5D Tandem Dual CAR-T
Participants receive treatment of In vivo BCMA/GPRC5D Tandem Dual CAR-T cell following a 3+3 dose-escalation design.
Administration of in vivo BCMA/GPRC5D tandem dual CAR-T cells. Three dose levels (dose A, dose B, dose C) will be evaluated using a standard 3+3 dose-escalation design.
Andere namen:
  • SL4903

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Number and incidence rate with Each Grade of Cytokine Release Syndrome (CRS)
Tijdsspanne: 1 month after treatment
CRS severity will be graded according to the American Society for Transplantation and Cellular Therapy (ASTCT) Consensus Grading. The grade ranges from 1 to 4, where a higher grade indicates a worse outcome.
1 month after treatment
Dose-limiting toxicities (DLTs)
Tijdsspanne: 1 month after treatment
Dose limiting toxicity will be assessed after injection
1 month after treatment
Number and incidence rate of Each Grade of Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS)
Tijdsspanne: 1 month after treatment
ICANS severity is graded according to the American Society for Transplantation and Cellular Therapy (ASTCT) Consensus Grading, which incorporates the Immune Effector Cell-Associated Encephalopathy (ICE) assessment. The ICE score ranges from 0 to 10, with higher scores indicating better cognitive function. ICANS grade ranges from 1 to 4, where a higher grade indicates a worse outcome.
1 month after treatment
Number and incidence rate of Treatment-Associated Adverse Events (AEs)
Tijdsspanne: 1 years after treatment
All other AEs would be assessed according to the Common Terminology Criteria for Adverse Events (CTCAE, Version 5.0).
1 years after treatment

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
overall survival (OS)
Tijdsspanne: 2 jaar na behandeling
Overall survival (OS) verwijst naar de tijd vanaf het begin van de behandeling tot het overlijden van de patiënt om welke reden dan ook.
2 jaar na behandeling
Overall Objective Response Rate (ORR)
Tijdsspanne: Day 14, Day 28, Month 2 , Month 3, Month 6, Month 9, Month 12, Month 18, Month24 after the treatment
Overall objective response rate (ORR) refers the sum of the proportions of complete remission (CR) and partial remission (PR).
Day 14, Day 28, Month 2 , Month 3, Month 6, Month 9, Month 12, Month 18, Month24 after the treatment
progression free survival (PFS)
Tijdsspanne: 2 years after treatment
Progression free survival (PFS) refers to the time from treatment to the first disease progression or death of the patient for any reason.
2 years after treatment
duration of response (DOR)
Tijdsspanne: 2 years after treatment
Duration of Response (DOR) refers to the time from the first assessment of plasma cell neoplasms as a complete or partial response to the first assessment of PD (Progressive Disease) or death from any cause.
2 years after treatment
time to progression (TTP)
Tijdsspanne: 2 years after treatment
Time to progression (TTP) refers to the time from treatment to the first plasma cell neoplasms progression.
2 years after treatment
recurrence rate
Tijdsspanne: 2 years after treatment
The recurrence rate refers to the proportion of patients with plasma cell neoplasms recurrence after treatment.
2 years after treatment
Cmax of CAR-T Cells
Tijdsspanne: 1 month after treatment
CAR-T kinetics would be detected by flow cytometry or qPCR in peripheral blood or bone marrow at each important time points. Cmax is the peak expansion value of CAR-T cells. Cmax is the peak expansion value of CAR-T cells.
1 month after treatment
Tmax of CAR-T Cells
Tijdsspanne: 1 month after treatment
CAR-T kinetics would be detected by flow cytometry or qPCR in peripheral blood bone marrow at each important time points. Tmax is the time of the occurrence of expansion peak.
1 month after treatment
AUC(0-28d)
Tijdsspanne: 1 month after treatment
AUC(0-28d) is the area under the peripheral blood CAR-T cell concentration versus time curve calculated from the time of treatment to 28 days post-treatment, using the linear trapezoidal method.
1 month after treatment

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Onderzoekers

  • Hoofdonderzoeker: Liping DOU, Chinese PLA General Hospital

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

9 mei 2026

Primaire voltooiing (Geschat)

31 maart 2029

Studie voltooiing (Geschat)

31 maart 2029

Studieregistratiedata

Eerst ingediend

20 april 2026

Eerst ingediend dat voldeed aan de QC-criteria

7 mei 2026

Eerst geplaatst (Werkelijk)

14 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

14 mei 2026

Laatste update ingediend die voldeed aan QC-criteria

7 mei 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • 2026-172-02

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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 .

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