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

7 mai 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Estimé)

18

Phase

  • Première phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

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).

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.
Autres noms:
  • SL4903

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Number and incidence rate with Each Grade of Cytokine Release Syndrome (CRS)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
survie globale (OS)
Délai: 2 ans après le traitement
La survie globale (OS) correspond à la période allant du début du traitement jusqu'au décès du patient, quelle qu'en soit la raison.
2 ans après le traitement
Overall Objective Response Rate (ORR)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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
Délai: 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
Délai: 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)
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chercheur principal: Liping DOU, Chinese PLA General Hospital

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

9 mai 2026

Achèvement primaire (Estimé)

31 mars 2029

Achèvement de l'étude (Estimé)

31 mars 2029

Dates d'inscription aux études

Première soumission

20 avril 2026

Première soumission répondant aux critères de contrôle qualité

7 mai 2026

Première publication (Réel)

14 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

14 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

7 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • 2026-172-02

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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