- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07586709
In Vivo BCMA/GPRC5D Tandem Dual CAR-T Therapy for Relapsed/Refractory Plasma Cell Neoplasms
7 maggio 2026 aggiornato da: 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.
Panoramica dello studio
Stato
Non ancora reclutamento
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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.
Tipo di studio
Interventistico
Iscrizione (Stimato)
18
Fase
- Prima fase 1
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Yu ZHAO
- Numero di telefono: 13601051848
- Email: zhaoyu301@126.com
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
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
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
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.
|
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:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Number and incidence rate with Each Grade of Cytokine Release Syndrome (CRS)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
sopravvivenza globale (OS)
Lasso di tempo: 2 anni dopo il trattamento
|
La sopravvivenza globale (OS) si riferisce al tempo trascorso dall'inizio del trattamento alla morte del paziente per qualsiasi motivo.
|
2 anni dopo il trattamento
|
|
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
|
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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Investigatore principale: Liping DOU, Chinese PLA General Hospital
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
9 maggio 2026
Completamento primario (Stimato)
31 marzo 2029
Completamento dello studio (Stimato)
31 marzo 2029
Date di iscrizione allo studio
Primo inviato
20 aprile 2026
Primo inviato che soddisfa i criteri di controllo qualità
7 maggio 2026
Primo Inserito (Effettivo)
14 maggio 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
14 maggio 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
7 maggio 2026
Ultimo verificato
1 maggio 2026
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 2026-172-02
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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