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
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Tipo di studio
Iscrizione (Stimato)
Iscrizione
Fase
Fase
- Prima fase 1
Contatti e Sedi
Contatto studio
Contatto studio
- Nome: Yu ZHAO
- Numero di telefono: 13601051848
- Email: zhaoyu301@126.com
Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
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).
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
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Sperimentale: 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.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Number and incidence rate with Each Grade of Cytokine Release Syndrome (CRS)
Lasso di tempo: 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)
Lasso di tempo: 1 month after treatment
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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)
Lasso di tempo: 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)
Lasso di tempo: 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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Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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sopravvivenza globale (OS)
Lasso di tempo: 2 anni dopo il trattamento
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La sopravvivenza globale (OS) si riferisce al tempo trascorso dall'inizio del trattamento alla morte del paziente per qualsiasi motivo.
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2 anni dopo il trattamento
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Overall Objective Response Rate (ORR)
Lasso di tempo: 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)
Lasso di tempo: 2 years after treatment
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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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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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Collaboratori e investigatori
Sponsor
Sponsor
Investigatori
Investigatori
- Investigatore principale: Liping DOU, Chinese PLA General Hospital
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Inizio studio
Completamento primario (Stimato)
Completamento primario
Completamento dello studio (Stimato)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- 2026-172-02
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