- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07586709
In Vivo BCMA/GPRC5D Tandem Dual CAR-T Therapy for Relapsed/Refractory Plasma Cell Neoplasms
7. mai 2026 oppdatert av: 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.
Studieoversikt
Status
Har ikke rekruttert ennå
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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
Intervensjonell
Registrering (Antatt)
18
Fase
- Tidlig fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Yu ZHAO
- Telefonnummer: 13601051848
- E-post: zhaoyu301@126.com
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
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
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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.
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Number and incidence rate with Each Grade of Cytokine Release Syndrome (CRS)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
overlevelse (OS)
Tidsramme: 2 år etter behandling
|
Overall survival (OS) refererer til tiden fra behandlingsstart til pasientens død av hvilken som helst årsak.
|
2 år etter behandling
|
|
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
|
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)
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.
|
2 years after treatment
|
|
duration of response (DOR)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Liping DOU, Chinese PLA General Hospital
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
9. mai 2026
Primær fullføring (Antatt)
31. mars 2029
Studiet fullført (Antatt)
31. mars 2029
Datoer for studieregistrering
Først innsendt
20. april 2026
Først innsendt som oppfylte QC-kriteriene
7. mai 2026
Først lagt ut (Faktiske)
14. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
14. mai 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
7. mai 2026
Sist bekreftet
1. mai 2026
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2026-172-02
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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