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

17 luglio 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Reclutamento

Intervento / Trattamento

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

15

Fase

  • 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

Luoghi di studio

    • Yunnan
      • Kunming, Yunnan, Cina
        • Reclutamento
        • 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
        • Contatto:

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:

  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.

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: CAR-T in vivo
I pazienti sono stati arruolati e hanno ricevuto una singola dose di iniezione CAR-T per via endovenosa, sono stati ricoverati in ospedale per l'osservazione nel mese successivo e sono stati seguiti per l'osservazione nei successivi 2 anni.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Maximal Tolerated Dose (MTD)
Lasso di tempo: 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
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective Response Rate (ORR)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: up to 24 months
OS is defined as the time from CAR-T infusion to death from any cause.
up to 24 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

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)

31 luglio 2026

Completamento primario (Stimato)

30 aprile 2028

Completamento dello studio (Stimato)

31 luglio 2028

Date di iscrizione allo studio

Primo inviato

14 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

17 luglio 2026

Primo Inserito (Effettivo)

20 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

20 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

17 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

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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