In Vivo BCMA/GPRC5D Tandem Dual CAR-T Therapy for Relapsed/Refractory Plasma Cell Neoplasms
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
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Tidlig fase 1
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Yu ZHAO
- Telefonnummer: 13601051848
- E-mail: zhaoyu301@126.com
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
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:
- Clonal plasma cells confirmed to be BCMA and/or GPRC5D positive by flow cytometry or immunohistochemistry;
- 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):
- Creatinine ≤ 2 × ULN;
- Left ventricular ejection fraction (LVEF) ≥ 50%;
- Oxygen saturation > 90%;
- 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).
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
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Eksperimentel: 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.
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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.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Number and incidence rate with Each Grade of Cytokine Release Syndrome (CRS)
Tidsramme: 1 month after treatment
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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.
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1 month after treatment
|
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Dose-limiting toxicities (DLTs)
Tidsramme: 1 month after treatment
|
Dose limiting toxicity will be assessed after injection
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1 month after treatment
|
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Number and incidence rate of Each Grade of Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS)
Tidsramme: 1 month after treatment
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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.
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1 month after treatment
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Number and incidence rate of Treatment-Associated Adverse Events (AEs)
Tidsramme: 1 years after treatment
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All other AEs would be assessed according to the Common Terminology Criteria for Adverse Events (CTCAE, Version 5.0).
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1 years after treatment
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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overlevelse (OS)
Tidsramme: 2 år efter behandling
|
Overall survival (OS) refererer til tiden fra behandlingens start til patientens død af enhver årsag.
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2 år efter behandling
|
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Overall Objective Response Rate (ORR)
Tidsramme: Day 14, Day 28, Month 2 , Month 3, Month 6, Month 9, Month 12, Month 18, Month24 after the treatment
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Overall objective response rate (ORR) refers the sum of the proportions of complete remission (CR) and partial remission (PR).
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Day 14, Day 28, Month 2 , Month 3, Month 6, Month 9, Month 12, Month 18, Month24 after the treatment
|
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progression free survival (PFS)
Tidsramme: 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.
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2 years after treatment
|
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duration of response (DOR)
Tidsramme: 2 years after treatment
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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.
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2 years after treatment
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time to progression (TTP)
Tidsramme: 2 years after treatment
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Time to progression (TTP) refers to the time from treatment to the first plasma cell neoplasms progression.
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2 years after treatment
|
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recurrence rate
Tidsramme: 2 years after treatment
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The recurrence rate refers to the proportion of patients with plasma cell neoplasms recurrence after treatment.
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2 years after treatment
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Cmax of CAR-T Cells
Tidsramme: 1 month after treatment
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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.
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1 month after treatment
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Tmax of CAR-T Cells
Tidsramme: 1 month after treatment
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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.
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1 month after treatment
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AUC(0-28d)
Tidsramme: 1 month after treatment
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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.
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1 month after treatment
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Efterforskere
Efterforskere
- Ledende efterforsker: Liping DOU, Chinese PLA General Hospital
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 2026-172-02
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