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CAR-T in Relapsed/Refractory Multiple Myeloma

4 luglio 2026 aggiornato da: Dr. Zaineb Akram

Pilot, Open-Label, Single-Arm Study of Autologous BCMA-Directed CAR-T Cells in Patients With Relapsed/Refractory Multiple Myeloma in Pakistan

The treatment options for multiple myeloma have evolved significantly over the years, providing patients with a range of therapies tailored to their specific circumstances. The choice of treatment often hinges on various factors, including the aggressiveness of the disease, individual prognostic indicators like genetic markers, the overall physical condition of the patient, and any pre-existing health issues that may affect treatment decisions. Current therapeutic strategies include several classes of drugs, each working through different mechanisms. Proteasome inhibitors (PIs) disrupt the protein degradation process within myeloma cells, thereby promoting their death. Immunomodulatory drugs (IMiDs) modulate the immune system and inhibit tumor growth by enhancing the body's natural anti-cancer responses. Monoclonal antibodies specifically target cancer cells, marking them for destruction by the immune system. In cases where patients are eligible, autologous stem cell transplantation remains a viable option, offering the potential for long-term remission by replacing damaged bone marrow with healthy stem cells from the patient's own body.

Despite these advancements, multiple myeloma continues to present significant challenges, as it often recurs even after initial successful treatment and remains an incurable disease. This highlights the urgent need for innovative therapeutic strategies that can effectively address resistance to existing treatments, ultimately aiming to improve patient outcomes and survival rates.

Panoramica dello studio

Stato

Reclutamento

Intervento / Trattamento

Descrizione dettagliata

Multiple myeloma is characterized by the synthesis of monoclonal immunoglobulin (Ig) proteins or their fragments, known as M proteins, which have lost their biological functionality. (Kyle & Rajkumar, 2008; Palumbo & Anderson, 2011).

The proliferation of multiple myeloma cells results in the gradual displacement of normal bone marrow hematopoietic precursors, which are essential for the production of blood cells. This displacement not only hampers the normal hematopoiesis process but also leads to an overproduction of M-proteins, which can have detrimental effects on the body's systems. Key characteristics of multiple myeloma include osteolytic lesions (areas of bone destruction that can lead to fractures and significant pain). Patients often experience anemia due to the impaired production of red blood cells, making them more prone to fatigue and weakness. Moreover, the disease can significantly increase susceptibility to infections, as the immune system becomes compromised. Additional complications include hypercalcemia (characterized by abnormally high calcium levels in the blood), which can lead to nausea and confusion. Renal insufficiency or failure is another serious consequence, often arising from the effects of M-proteins on kidney function. Lastly, neurological complications can occur, manifesting as various symptoms ranging from peripheral neuropathy to more severe neurological deficits. Collectively, these manifestations highlight the complex and multifaceted impact of multiple myeloma on patients' health. (Korde et al., 2011; Palumbo & Anderson, 2011) In the year 2022, a total of 187,952 cases of Multiple Myeloma (MM) were documented across the globe, representing approximately 0.94% of all cancer cases reported internationally. This hematological malignancy exhibits notable geographical variations in its incidence rates. Notably, Asia accounted for the highest number of cases, with 73,870 reported instances, which corresponds to 39.3% of the global total. Europe and Northern America followed, with 50,092 cases (26.7%) and 37,050 cases (19.7%), respectively. Among the countries in the Eastern Mediterranean Region (EMRO), Pakistan has reported the highest rates of incidence (25.3%) and mortality (26.3%) for Multiple Myeloma (MM). In Pakistan, there were 1,846 new cases of Multiple Myeloma and 1,616 deaths attributed to this disease. These statistics highlight the clinical and epidemiological importance of MM both regionally and globally. They emphasize the ongoing need for research and healthcare strategies aimed at improving patient outcomes and understanding the factors contributing to the incidence and mortality of this complex disease. (Global Cancer Observatory, 2024).

Figure 01: Absolute numbers, Incidence of Multiple Myeloma in EMRO, both sexes, in 2022 (Global Cancer Observatory, 2024).

Figure 02: Absolute numbers, Mortality rate due to Multiple Myeloma in EMRO, both sexes, in 2022 (Global Cancer Observatory, 2024).

The treatment options for multiple myeloma have evolved significantly over the years, providing patients with a range of therapies tailored to their specific circumstances. The choice of treatment often hinges on various factors, including the aggressiveness of the disease, individual prognostic indicators like genetic markers, the overall physical condition of the patient, and any pre-existing health issues that may affect treatment decisions. Current therapeutic strategies include several classes of drugs, each working through different mechanisms. Proteasome inhibitors (PIs) disrupt the protein degradation process within myeloma cells, thereby promoting their death. Immunomodulatory drugs (IMiDs) modulate the immune system and inhibit tumor growth by enhancing the body's natural anti-cancer responses. Monoclonal antibodies specifically target cancer cells, marking them for destruction by the immune system. In cases where patients are eligible, autologous stem cell transplantation remains a viable option, offering the potential for long-term remission by replacing damaged bone marrow with healthy stem cells from the patient's own body.

Despite these advancements, multiple myeloma continues to present significant challenges, as it often recurs even after initial successful treatment and remains an incurable disease. This highlights the urgent need for innovative therapeutic strategies that can effectively address resistance to existing treatments, ultimately aiming to improve patient outcomes and survival rates.

4.2. BCMA B Cell Maturation Antigen (BCMA), also known as TNFRSF17, is a vital membrane protein intricately involved in the survival and proliferation of B lineage cells. This essential protein interacts with two key ligands: the proliferation-inducing ligand (APRIL) and the B-cell activating factor (BAFF). Both ligands play a crucial role in promoting the growth and longevity of plasma cells, which are critical components of the immune system (Tai & Anderson, 2015).

Recent research has highlighted the significant therapeutic potential of targeting BCMA as a treatment strategy for multiple myeloma (MM). Advances in this domain have led to the development of innovative BCMA-targeted therapies, including engineered CAR T-cell therapy and bispecific T-cell engagers. These groundbreaking approaches have demonstrated impressive efficacy in early-phase clinical trials, resulting in durable responses among patients with advanced, heavily pre-treated MM (Patel et al., 2004; Avery et al., 2003).

4.3. CAR-T Therapy The Chimeric Antigen Receptor T-cell (CAR-T) therapy represents a groundbreaking advancement in the field of immunotherapy, specifically designed to harness the patient's own immune system to target and eliminate cancer cells. This innovative approach involves genetically modifying a patient's T cells so they can express a chimeric antigen receptor that specifically recognizes antigens present on the tumor cells.

Mechanism of Action The CAR-T process typically begins with the collection of T cells from the patient through a procedure known as apheresis. The collected T cells are then genetically engineered in a laboratory setting to produce Chimeric Antigen Receptors (CARs) that can recognize specific cancer markers, such as CD19, in B-cell malignancies such as acute lymphoblastic leukemia (ALL) and certain types of non-Hodgkin lymphoma. Once engineered, these CAR-T cells are expanded in number and subsequently infused back into the patient. Upon reintroduction, the CAR-T cells patrol the body for cancer cells expressing the target antigen, initiating an immune response that can lead to cellular lysis of the malignant cells (June et al., 2018).

Clinical Efficacy CAR-T therapy has shown remarkable success, particularly in hematologic malignancies. For example, studies have reported overall response rates (ORR) exceeding 80% in patients with relapsed or refractory ALL after treatment with CAR-T cells targeting CD19 (Kymriah®) (Schuster et al., 2019). Similarly, in patients with large B-cell lymphoma, the CAR-T product axicabtagene ciloleucel (Yescarta®) also demonstrated impressive efficacy, with a median progression-free survival of 6.5 months and an ORR of 82% (Zuma-1 trial) (Zuma et al., 2017).

Tipo di studio

Interventistico

Iscrizione (Stimato)

10

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

  • Nome: Maryam Khan, MBBS, MRCP(UK), FCPS (Cl Haem)
  • Numero di telefono: +923366395758

Luoghi di studio

    • Punjab Province
      • Rawalpindi, Punjab Province, Pakistan, 46000
        • Reclutamento
        • National University of Medical Sciences, Clinical Trial Unit
        • Contatto:
        • Contatto:
        • Investigatore principale:
          • Tariq Ghafoor, MBBS,FCPS,FRCP(Ire),FRCP(Glas)
        • Sub-investigatore:
          • Raheel Iftikhar, MBBS,FCPS(Med),FCPS(Cl Haem)
        • Sub-investigatore:
          • Hammad Javed, MBBS,FCPS(Med), FCPS(Cl Haem)
        • Sub-investigatore:
          • Memoona Khan, MBBS, FCPS (Haem)
        • Sub-investigatore:
          • Aamir Aslam Awan, MBBS,FCPS(Paeds)
        • Sub-investigatore:
          • Nadia Sial, PhD
        • Sub-investigatore:
          • Arif Sadiq, MBBS,FCPS(Haem),FCPS(CL Haem)
        • Sub-investigatore:
          • Saleem Ahmed Khan, MBBS,FCPS
        • Sub-investigatore:
          • Babar Saeed Khan, MBBS

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. Male and female participants of age 18 years and above.
  2. Patients with a confirmed diagnosis of multiple myeloma according to IMWG diagnostic criteria.
  3. Received at least 3 prior multiple myeloma treatment lines of therapy or are double refractory to an IMiD and PI (refractory multiple myeloma as defined by IMWG consensus criteria). Note: induction with or without hematopoietic stem cell transplant and with or without maintenance therapy is considered a single line of therapy.
  4. Measurable disease at Screening as per IMWG criteria.
  5. ECOG Performance Status grade of 0 to 2.
  6. Adequate organ function: ANC/platelets thresholds (unless cytopenias attributable to MM), LVEF ≥45%, adequate oxygenation; hepatic/renal criteria specified in Section 10.
  7. Negative pregnancy test for women of childbearing potential; agreement to effective contraception.
  8. Patients giving written informed consent to participate in the study after a full understanding of the implications and constraints of the study protocol.
  9. Understand the content of the ICF, and voluntarily sign the ICF (If the participant is unable to sign the ICF on their own due to illiteracy, an impartial witness is needed).
  10. The subject can understand the research process and is willing and able to comply with all research proposals and other requirements of the study.
  11. Willing and able to adhere to the prohibitions and restrictions specified in this protocol.

Exclusion Criteria

1. Patients who will meet any of the following criteria will not be eligible to participate in the study.

  1. Prior treatment with CAR-T therapy directed at any target. Any therapy that is targeted to BCMA.
  2. Known active, or prior history of central nervous system (CNS) involvement, or exhibits clinical signs of meningeal involvement of multiple myeloma.
  3. Stroke or seizure within 6 months of signing the ICF.
  4. Uncontrolled active infection, including uncontrolled bacterial or fungal infection; active uncontrolled HBV/HCV/HIV.
  5. Clinically significant cardiac disease (e.g., NYHA III/IV, recent MI), or severe pulmonary disease.
  6. Recent allogeneic HSCT with active GVHD or ongoing immunosuppression.
  7. Pregnant or breast-feeding, or planning to become pregnant while enrolled in this study or within 1 year after receiving study treatment.
  8. Any other circumstances that would impair the ability of the participant to receive or tolerate the planned treatment at the investigational site, to understand informed consent, or any condition for which, in the opinion of the investigator, participation would not be in the best interest of the participant (e.g., compromise the well-being) or that could prevent, limit, or confound the protocol-specified assessments.

    -

    Exclusion Criteria:

    -

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
Altro: CAR-T arm

6.2. Screening Phase During the Screening period, all participants will be asked to provide written consent for study participation and will be screened for study eligibility within 28 days before apheresis. Safety criteria that must be met before starting apheresis are presented in Section 8.1.1.

If an assessment was performed as part of the participant's routine clinical evaluation and not specifically for this study, it does not need to be repeated after signed informed consent has been obtained, provided the assessments fulfill the study requirements and are performed within the specified timeframe before the first dose of study treatment. Retesting of abnormal screening values that lead to exclusion is allowed only once during the screening phase (to reassess eligibility). The last result obtained before apheresis will be used to determine eligibility. Subjects who do not meet all inclusion criteria or who meet an exclusion criterion may, at the discretion of the investigator,

CAR-T therapy will be given

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Assess Safety /tolerability and feasibility of manufacturing and delivering the product
Lasso di tempo: From enrolment to 1 years after infusion of the product
incidence/severity of AEs including CRS/ICANS (ASTCT grading), DLTs through Day +28
From enrolment to 1 years after infusion of the product

Collaboratori e investigatori

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

Investigatori

  • Cattedra di studio: Maryam Khan, MBBS, MRCP (UK), FCPS(Cl Haem), National University of Medical Sciences
  • Investigatore principale: Tariq Ghafoor, National University of Medical Sciences

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

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 (Effettivo)

1 giugno 2026

Completamento primario (Stimato)

31 dicembre 2027

Completamento dello studio (Stimato)

31 dicembre 2027

Date di iscrizione allo studio

Primo inviato

27 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

4 luglio 2026

Primo Inserito (Effettivo)

8 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

8 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

4 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)?

SÌ

Descrizione del piano IPD

IPD will be shared on request by email.

Periodo di condivisione IPD

after 31st December 2027 till 31st December 2028

Criteri di accesso alla condivisione IPD

Access will be given by requesting PI by email

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA
  • ICF

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

prodotto fabbricato ed esportato dagli 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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