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In Vivo PICX CAR-T Therapy for R/R Multiple Myeloma

17 de julho de 2026 atualizado por: Chongqing Precision Biotech Co., Ltd

In Vivo Prepared PICX Chimeric Antigen Receptor T-Cell Therapy for the Treatment of Relapsed/Refractory Multiple Myeloma

This study is an investigator-initiated, single-center, single-arm clinical study with a target population of patients with relapsed or refractory multiple myeloma.

It is an early exploratory clinical study evaluating the safety, tolerability, and preliminary efficacy of PICX Injection, an in vivo prepared CAR-T cell therapy, in the treatment of relapsed or refractory multiple myeloma.

Visão geral do estudo

Status

Recrutamento

Intervenção / Tratamento

Descrição detalhada

This is a prospective, open-label, single-arm clinical investigation to assess the safety and efficacy of in vivo CAR-T cell therapy in patients with relapsed or refractory multiple myeloma.

Eligible subjects will be treated with PICX Injection as a single intravenous infusion. Post-infusion, subjects will remain hospitalized for close observation and undergo serial evaluations for adverse events and treatment response. Long-term follow-up will continue for up to 2 years to assess disease status and durability of response.

Tipo de estudo

Intervencional

Inscrição (Estimado)

15

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Yunnan
      • Kunming, Yunnan, China
        • Recrutamento
        • 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  1. Age ≥ 18 years, male or female;
  2. Confirmed diagnosis of multiple myeloma meeting at least one of the following criteria:

    1. Disease progression after at least 2 prior standard treatment regimens; or poor response to primary therapeutic agents (e.g., immunomodulatory agents, proteasome inhibitors)
    2. Disease progression within 18 months after first-line therapy
    3. Presence of features associated with high risk of disease relapse or progression (e.g., high-risk cytogenetic abnormalities);
  3. At least one measurable disease indicator:

    1. Serum M-protein ≥ 0.5 g/dL
    2. Urine M-protein ≥ 200 mg/24 hours
    3. Involved serum free light chain (sFLC) ≥ 10 mg/dL with an abnormal serum free light chain κ/λ ratio
  4. No evidence of extramedullary plasmacytoma (soft tissue plasmacytoma);
  5. ECOG performance status score 0-2;
  6. Expected survival period ≥ 3 months;
  7. Adequate bone marrow function within 1 month prior to screening:

    1. Hemoglobin ≥ 60 g/L;
    2. Absolute neutrophil count (ANC) ≥ 0.5 × 10⁹/L;
    3. Platelet count (PLT) ≥ 50 × 10⁹/L;
    4. Lymphocyte count ≥ 0.5 × 10⁹/L;
    5. CD3-positive T-cell absolute count ≥ 0.15 × 10⁹/L;
  8. Adequate vital organ function within 1 month prior to screening:

    1. Renal function: creatinine clearance rate (CrCl) ≥ 30 mL/min (calculated using the Cockcroft-Gault formula), or serum creatinine (Scr) ≤ 2.0 × upper limit of normal (ULN);
    2. Hepatic function: alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3.0 × ULN; total bilirubin (TBIL) ≤ 2.0 × ULN (except for patients with congenital hyperbilirubinemia such as Gilbert's syndrome, in which case direct bilirubin may be ≤ 1.5 × ULN);
    3. Cardiac function: left ventricular ejection fraction (LVEF) ≥ 40%; no clinically significant pericardial effusion; and no clinically significant electrocardiogram (ECG) abnormalities (e.g., severe arrhythmia, myocardial ischemia, conduction block);
    4. Pulmonary function: blood oxygen saturation (SpO₂) ≥ 90% without supplemental oxygen;
  9. Women of childbearing potential must have a negative pregnancy test during the screening period and before study drug administration, and must not be lactating during the study;
  10. Men and women of childbearing potential must agree to use effective contraceptive measures (excluding unreliable methods such as rhythm method) from the time of signing the informed consent form until 1 year after the last dose of study drug, and must agree not to donate sperm or eggs;
  11. The subject or their legally authorized representative has signed the informed consent form (ICF), indicating understanding of the study purpose and procedures and voluntary participation.

Exclusion Criteria:

  1. Prior treatment with CAR-T therapy or other gene-modified cell therapy before screening;
  2. Presence of active central nervous system (CNS) involvement at screening (including brain parenchymal, meningeal, or spinal meningeal involvement, or positive cerebrospinal fluid for tumor cells), or other CNS diseases;
  3. Received the following anti-tumor therapies prior to PICX Injection infusion:

    1. Chemotherapy, combination therapy with proteasome inhibitors and immunomodulatory agents, or other systemic anti-tumor drug therapy within 14 days or at least 5 half-lives before infusion (excluding intrathecal chemotherapy, which must be discontinued at least 1 week prior to infusion);
    2. Radiotherapy to non-hematopoietic sites within 7 days, or to hematopoietic sites within 14 days before infusion;
    3. BCMA-targeting antibody-based therapy within 3 months before infusion;
  4. Active or uncontrolled infection requiring systemic treatment at screening (including bacterial, viral, fungal, or other infections);
  5. Presence of any of the following cardiac conditions:

    1. New York Heart Association (NYHA) Class III or IV congestive heart failure;
    2. Myocardial infarction, or coronary artery bypass grafting (CABG), or coronary stent placement within 6 months prior to screening;
    3. Clinically significant ventricular arrhythmia, or history of syncope of unknown cause (excluding vasovagal or dehydration-related);
    4. History of severe non-ischemic cardiomyopathy;
  6. Presence of other clinically significant diseases or conditions, including:

    1. Primary immunodeficiency disease;
    2. Cerebrovascular accident or seizure within 6 months prior to screening;
    3. Definite cognitive impairment or psychiatric/behavioral abnormalities (e.g., dementia, altered mental status), or severe psychiatric disorders;
    4. Parkinson's disease, Parkinsonism, or other movement disorders;
  7. Grade 2-4 acute graft-versus-host disease (GVHD) or moderate to severe chronic GVHD within 4 weeks prior to screening;
  8. History of other malignancies other than multiple myeloma prior to screening, except for:

    1. Malignancies treated with curative intent with no known active disease for ≥ 2 years prior to enrollment;
    2. Adequately treated cervical carcinoma in situ, basal cell or squamous cell skin carcinoma, localized prostate cancer after radical surgery, or ductal carcinoma in situ after radical surgery;
  9. Vaccination with live-attenuated vaccine within 4 weeks prior to screening;
  10. Known severe hypersensitivity to PICX Injection or any of its formulation components;
  11. Inability to establish venous access;
  12. Other conditions deemed by the investigator to be unsuitable for participation in the study.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: CAR-T in vivo
Os doentes foram inscritos e receberam uma dose única de injeção de CAR-T por via intravenosa, hospitalizados para observação durante o mês seguinte, e acompanhados para observação durante os 2 anos seguintes.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Maximal Tolerated Dose (MTD)
Prazo: Up to 28 days after infusion
MTD will be determined based on Dose-Limiting Toxicity (DLTs) observed during the first 28 days of study treatment.
Up to 28 days after infusion
Incidence of Adverse Events (AE) after infusion
Prazo: Up to 28 days after infusion
The frequency, severity, and laboratory findings of all adverse events/serious adverse events are included.
Up to 28 days after infusion

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Objective Response Rate (ORR)
Prazo: Day 28#Month 2#Month 3#Month 6#Month 12#Month 18#Month 24
ORR is defined as the proportion of subjects achieving stringent complete remission (sCR), complete remission (CR), very good partial response (VGPR), and partial response (PR) per IMWG response criteria (2016).
Day 28#Month 2#Month 3#Month 6#Month 12#Month 18#Month 24
Minimal Residual Disease (MRD) Negative Rate
Prazo: Month 3#Month 6#Month 12#Month 18#Month 24
MRD negativity rate is defined as the proportion of subjects achieving MRD-negative status as assessed by next-generation flow cytometry or sequencing.
Month 3#Month 6#Month 12#Month 18#Month 24
Time to Response (TTR)
Prazo: Up to 24 months
TTR is defined as the time from CAR-T infusion to first documented response (PR or better).
Up to 24 months
Duration of Response (DOR)
Prazo: up to 24 months
DOR is defined as the time from first documented response (PR or better) to first documented disease progression or death from any cause.
up to 24 months
Progression-Free Survival (PFS)
Prazo: up to 24 months
PFS is defined as the time from CAR-T infusion to first documented disease progression or death from any cause.
up to 24 months
Overall Survival (OS)
Prazo: up to 24 months
OS is defined as the time from CAR-T infusion to death from any cause.
up to 24 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

31 de julho de 2026

Conclusão Primária (Estimado)

30 de abril de 2028

Conclusão do estudo (Estimado)

31 de julho de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

14 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

17 de julho de 2026

Primeira postagem (Real)

20 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

20 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

17 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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