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Isatuximab, Iberdomide, Bortezomib, Dexamethasone in Transplant Ineligible/Deferred Newly Diagnosed Myeloma (IsaIberVD)

1 de setembro de 2026 atualizado por: Clifton Mo, MD, Dana-Farber Cancer Institute

A Phase 1b/2 Study of the Combination Isatuximab, Iberdomide, Bortezomib, and Dexamethasone in Newly Diagnosed Multiple Myeloma Who Are Transplant Ineligible or Not Intended for Upfront Transplant

This study is to evaluate the combination of isatuximab, iberdomide, bortezomib, and dexamethasone in newly diagnosed multiple myeloma participants who are transplant ineligible or not intended for upfront transplant.

The names of the study drugs used in this research study are:

isatuximab, iberdomide, bortezomib dexamethasone

Visão geral do estudo

Descrição detalhada

This is an open-label, Phase 1b/2, multicenter study which will enroll patients with newly diagnosed multiple myeloma (NDMM), who are transplant ineligible or deferred, to induction followed by maintenance therapy. Participants will be registered in HCC CTMS OnCore before receiving any study-specific treatment, and study treatment is expected to begin within 5 days after registration.

The study drugs used in this research include bortezomib, dexamethasone, isatuximab, and iberdomide (CC-220). The U.S. Food and Drug Administration (FDA) has approved bortezomib and dexamethasone for the initial treatment of multiple myeloma. The FDA has approved isatuximab for initial treatment of multiple myeloma in transplant ineligible patients and for myeloma that has returned after prior treatment. The FDA has not approved iberdomide (CC-220) for the treatment of multiple myeloma. The combination of these drugs, used as induction and maintenance therapy in this study, is considered investigational.

The research study procedures include: screening for eligibility, in-clinic visits, urine tests, questionnaires, PET scans, blood tests, electrocardiograms (ECGs), bone marrow aspiration and biopsy, biobanking, and pregnancy tests for participants who are able to become pregnant.

It is expected that about 88 people will take part in this study. Participants are classified and assigned treatment for induction based on baseline age 70 years status and myeloma frailty score and further assigned for maintenance based on baseline International Myeloma Working Group (IMWG)/International Myeloma Society (IMS) genomic risk classification.

Tipo de estudo

Intervencional

Inscrição (Estimado)

88

Estágio

  • Fase 2
  • 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

Estude backup de contato

Locais de estudo

    • Massachusetts
      • Boston, Massachusetts, Estados Unidos, 02215
        • Dana-Farber Cancer Institute
        • Contato:
        • Investigador principal:
          • Cliford Mo, MD
      • Boston, Massachusetts, Estados Unidos, 02215
        • Beth Israel Deaconess Medical Center (Bidmc)
        • Investigador principal:
          • David Avigan, MD
        • 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:

  • Male or female, 18 years of age or older
  • Ability to understand and the willingness to sign a written informed consent document
  • NDMM based on IMWG criteria with clonal bone marrow plasma cells >10% or biopsy proven bony or extramedullary disease/plasmacytoma (EMD) with any one or more CRAB-features or myeloma defining events (Rajkumar, 2024). (See Appendix G)
  • Ineligible for ASCT as assessed by the treating physician or eligible but prefers and agrees to defer ASCT until after induction and maintenance therapy, upon progression or at a later time
  • Measurable disease defined as at least one of the following:

    • Serum M-protein 0.5 g/dL
    • Urine M-protein 200 mg/24 hours
    • Serum FLC assay: involved FLC 10 mg/dL (100 mg/L) and an abnormal kappa to lambda FLC ratio (< 0.26 or > 1.65)
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (See Appendix A)
  • Screening Laboratory evaluations with the following parameters:

    • Absolute neutrophil count (ANC) ≥ 1,000 cells/dL (1.0 x 109/L)

      --- Note: Growth factor support is not permitted within 10 days, [14 days for pegfilgrastim], prior to the screening hematologic test.

    • Platelet count ≥ 75,000 cells/dL (75 x 109/L) (without transfusions required during the 3 days prior to the screening hematologic test)
    • Total Bilirubin ≤ 2 X upper limit of normal (ULN) (except patients with Gilbert Syndrome, who can have total bilirubin < 3.0 mg/dL)
    • AST (SGOT) and ALT (SGPT) ≤ 3.0 x ULN
    • Calculated creatinine clearance (CrCl) 30ml/min (Appendix B)
    • Hemoglobin ≥ 8.0 g/dl (red blood cell (RBC) transfusions are permitted)
  • Individuals of childbearing potential (IOCBP) must have 2 negative pregnancy tests before initiation of therapy, and agree to ongoing testing, based on the frequency outlined in the Pregnancy Prevention Plan (PPP) (See Appendix H)
  • Sexually active IOCBP agree to use protocol-specified contraceptive methods, at least 28 days prior to starting study drug, while taking study drug, including interruptions in study drugs, and for at least 28 days after the last dose of study drug or males sexually active with IOCBP, (including those who have had a vasectomy), agree to use protocol specified contraceptive methods while taking study drug, including interruptions in study drug and for at least 28 days after the last dose of iberdomide, 5 months after isatuximab and 6 months after bortezomib, according to the PPP (See Appendix H)
  • All patients (male and female with or without childbearing potential) agree to counseling according to the PPP and to abstain from donating blood products for at least 28 days after the last dose of iberdomide and abstain from donating semen or sperm while taking study drug and for at least 28 days after the last dose of iberdomide according to the PPP (See Appendix H) and for 5 months after the last dose of isatuximab and 6 months after the last dose of bortezomib
  • Must be able to take antithrombotic prophylaxis (See Section 5.9.1)

Exclusion Criteria:

  • Prior therapy for MM. Patients may have received:

    • Corticosteroids for management of MM not to exceed equivalent of 160 mg of dexamethasone in a 2-week period and should be stable 7 days prior to the registration.
    • Focal palliative radiation for the management of bone pain completed ≥ 7 days prior to registration
    • Treatment for smoldering myeloma as long as the prior treatment did not include anti-CD38 therapy:

      • Patients with a prior history of serious allergic reactions associated with thalidomide, lenalidomide, or pomalidomide should not receive iberdomide as they could be at higher risk of hypersensitivity.
      • Resolution of symptoms of prior treatment to ≤ grade 1 or baseline
  • Known intolerance to steroid therapy
  • Prior history of malignancies, other than MM, will be excluded unless the participant has been free of the disease for ≥ 3 years with the exception of the following non-invasive malignancies: basal or squamous cell skin carcinoma, carcinoma in situ of the cervix, carcinoma in situ of the breast, incidental histological findings of prostate cancer (T1a or T1b using the Tumor, Node, Metastasis (TNM) clinical staging system), or prostate cancer that is curative
  • Central nervous system involvement with MM
  • Peripheral neuropathy grade 3, or grade 2 with pain on clinical exam during screening period
  • Any medical or psychiatric illness that in the investigator's opinion would impose excessive risk to the patient or would adversely affect participation
  • Concurrent uncontrolled cardiovascular conditions (uncontrolled hypertension, uncontrolled arrhythmias, congestive heart failure, unstable angina, grade 3 thromboembolic event or myocardial infarction) in the past 6 months
  • Concurrent symptomatic amyloidosis or plasma cell leukemia
  • POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein and skin changes)
  • Seropositive for human immunodeficiency virus (HIV-1), chronic or active hepatitis B (defined as positive hepatitis B surface antigen (HepBSAg) or Hepatitis B core antibody (HepBcore Ab) or C (Hep C Ab), or acute hepatitis A. If any history of exposure to hepatitis B or C, then PCR should be negative
  • Pregnant or breast feeding female or IOCBP who intend to become pregnant during the study.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to other agents used in 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: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Group A Induction: Age <70 years and Fit (standard-intensity schedule)

Participants <70 years of age and considered fit based on the myeloma frailty score of 0.

Induction cycles 1-8; 28-day cycles:

Isatuximab: 10 mg/kg Intravenous (IV) Days 1, 8, 15, 22 (Cycle 1 only); Days 1,15 (Cycle 2+)

Iberdomide: 1 mg or 0.75 mg Oral (PO) Days 1-21

Bortezomib: 1.3 mg/m2 Subcutaneous (SC) Days 1, 8, 15, 22

Dexamethasone: 20 mg IV or PO Days 1, 2, 8, 9, 15, 16, 22, 23

Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Sarclisa
  • Isatuximabe-irfc
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • CC-220
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Velcade
  • PS-341
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Decadron
Experimental: Group B Induction: Age ≥70 years and/or Intermediate Fit/Frail (reduced-intensity schedule)

Participants ≥70 years of age and/or considered intermediate fitness and frail based on the myeloma frailty score of >1.

Induction cycles 1-8; 28-day cycles:

Isatuximab: 10 mg/kg IV Days 1, 8, 15, 22 (Cycle 1 only); Days 1,15 (Cycle 2+)

Iberdomide: 1 mg or 0.75 mg PO Days 1-21

Bortezomib: 1.3 mg/m2 SC Days 1, 8, 15

Dexamethasone: 12 mg IV or PO Days 1, 8, 15, 22; 8 mg IV or PO Days 2, 9, 16, 23

Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Sarclisa
  • Isatuximabe-irfc
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • CC-220
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Velcade
  • PS-341
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Decadron
Experimental: Group A Maintenance: High-Risk, Age <70 years and Fit (3-drug schedule)

Participants high-risk per IMWG/IMS criteria, <70 years of age, considered fit based on the myeloma frailty score of 0.

Maintenance cycles 1-36; 28-day cycles:

(for participants with ≥PR after Induction Cycle 8)

Isatuximab: 10 mg/kg IV Days 1, 15

Iberdomide: 1 mg or 0.75 mg PO Days 1-21

Bortezomib: 1.3 mg/m2 SC Days 1, 15

Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Sarclisa
  • Isatuximabe-irfc
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • CC-220
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Velcade
  • PS-341
Experimental: Group A Maintenance: Standard-Risk, Age <70 years and Fit (2-drug schedule)

Participants standard-risk per IMWG/IMS criteria, <70 years of age, considered fit based on the myeloma frailty score of 0.

Maintenance cycles 1-36; 28-day cycles:

(for participants with ≥PR after Induction Cycle 8)

Isatuximab: 10 mg/kg IV Days 1, 15

Iberdomide: 1 mg or 0.75 mg PO Days 1-21

Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Sarclisa
  • Isatuximabe-irfc
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • CC-220
Experimental: Group B Maintenance: High-Risk, Age ≥70 years and/or Intermediate Fit/Frail (3-drug schedule)

Participants high-risk per IMWG/IMS criteria, ≥70 years of age and/or considered intermediate fitness and frail based on the myeloma frailty score of >1.

Maintenance cycles 1-36; 28-day cycles:

(for participants with ≥PR after Induction Cycle 8)

Isatuximab: 10 mg/kg IV Days 1, 15

Iberdomide: 1 mg or 0.75 mg PO Days 1-21

Bortezomib: 1.3 mg/m2 SC Days 1, 15

Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Sarclisa
  • Isatuximabe-irfc
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • CC-220
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Velcade
  • PS-341
Experimental: Group B Maintenance: Standard-Risk, Age ≥70 years and/or Intermediate Fit/Frail (2-drug schedule)

Participants standard-risk per IMWG/IMS criteria, ≥70 years of age and/or considered intermediate fitness and frail based on the myeloma frailty score of >1.

Maintenance cycles 1-36; 28-day cycles:

(for participants with ≥PR after Induction Cycle 8)

Isatuximab: 10 mg/kg IV Days 1, 15

Iberdomide: 1 mg or 0.75 mg PO Days 1-21

Administration, pre-medications and supportive care per protocol
Outros nomes:
  • Sarclisa
  • Isatuximabe-irfc
Administration, pre-medications and supportive care per protocol
Outros nomes:
  • CC-220

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Dose-limiting Toxicities (DLT) by Age-Frailty Group [Phase Ib]
Prazo: Assessed continuously during induction cycle 1, up to day 28 + 30 days
DLT is defined as any adverse event (AE) that (a) is at least possibly related to study treatment, (b) occur during cycle 1, and (c) meets the following criteria: Hematologic - grade 4 neutropenia lasting >5 days despite supportive care (G-CSF allowed), grade ≥3 febrile neutropenia, grade 3 thrombocytopenia with clinically significant bleeding, grade 4 thrombocytopenia unless clearly attributable to underlying disease, and any grade 5 AE; Non-Hematologic - any grade ≥3 AE (except alopecia), uncontrolled nausea, vomiting, or diarrhea not resolving to ≤ grade 1 with medical management, due to toxicity interruption of >4 doses of iberdomide or >1 dose of isatuximab or bortezomib (infusion-related reactions excluded), due to toxicity inability to initiate cycle 2 day 1 within 7 days.
Assessed continuously during induction cycle 1, up to day 28 + 30 days
Recommended Phase II Dose (RP2D) of Iberdomide by Age-Frailty Group [Phase Ib]
Prazo: Assessed continuously during induction cycle 1, up to day 28 + 30 days
The RP2D of iberdomide in combination with fixed doses of isatuximab, bortezomib and dexamethasone is determined by the number of participants experiencing DLT. There are two potential iberdomide dose levels under evaluation including one de-escalation dose. The RP2D is defined as the highest dose at which fewer than 2 of 6 patients experience a DLT.
Assessed continuously during induction cycle 1, up to day 28 + 30 days
Complete Response (CR) or Better Rate by Age-Frailty Group [Phase II]
Prazo: Assessed on day 1 of each cycle over 8 induction cycles (cycle duration=4 weeks), up to 32 weeks.
CR or better rate is defined as the proportion of participants who achieve a complete response (CR) or stringent CR (sCR) during induction therapy, according to the International Myeloma Working Group Uniform Response Criteria (IMWG-URC).
Assessed on day 1 of each cycle over 8 induction cycles (cycle duration=4 weeks), up to 32 weeks.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Induction Grade 3 or 4 Treatment-Related Adverse Event (TRAE) Rate by Age-Frailty Group [Phase Ib]
Prazo: Assessed continuously during induction cycles 1-8 (cycle duration=4 weeks), up to 32 weeks + 30 days.
Induction grade 3 or 4 TRAE rate is defined as the proportion of participants who experience a grade 3 or 4 AE based on Common Toxicity Criteria for Adverse Events version 5 (CTCAEv5) with a treatment attribution of possible, probable or definite during induction.
Assessed continuously during induction cycles 1-8 (cycle duration=4 weeks), up to 32 weeks + 30 days.
Induction Feasibility Rate by Age-Frailty Group [Phase II]
Prazo: Assessed after induction cycle 8 (cycle duration=4 weeks), at 32 weeks plus 30 days.
Induction feasibility rate is defined as the proportion of participants completing 8 cycles of induction and receiving at least one dose of maintenance treatment.
Assessed after induction cycle 8 (cycle duration=4 weeks), at 32 weeks plus 30 days.
Induction Grade 3 or 4 TRAE Rate by Age-Frailty Group [Phase II]
Prazo: Assessed continuously during induction cycles 1-8 (cycle duration=4 weeks), up to 32 weeks + 30 days.
Induction grade 3 or 4 TRAE rate is defined as the proportion of participants who experience a grade 3 or 4 AE based on CTCAEv5 with a treatment attribution of possible, probable or definite during induction.
Assessed continuously during induction cycles 1-8 (cycle duration=4 weeks), up to 32 weeks + 30 days.
Maintenance Grade 3 or 4 TRAE Rate by Age-Frailty Risk Group [Phase II]
Prazo: Assessed continuously during maintenance cycles 1-36 (cycle duration=4 weeks), up to 144 weeks + 30 days.
Maintenance grade 3 or 4 TRAE rate is defined as the proportion of participants who experience a grade 3 or 4 AE based on CTCAEv5 with a treatment attribution of possible, probable or definite during maintenance.
Assessed continuously during maintenance cycles 1-36 (cycle duration=4 weeks), up to 144 weeks + 30 days.
Induction Serious Adverse Event (SAE) Rate by Age-Frailty Group [Phase II]
Prazo: Assessed continuously during induction cycles 1-8 (cycle duration=4 weeks), up to 32 weeks + 30 days.
Induction SAE is any untoward medical occurrence at any dose during induction that: results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization (excluding planned hospitalizations), results in persistent or significant disability or incapacity (namely a substantial disruption of normal life functions), is a congenital anomaly or birth defect, or is considered a medically important event.
Assessed continuously during induction cycles 1-8 (cycle duration=4 weeks), up to 32 weeks + 30 days.
Maintenance SAE Rate by Age-Frailty Risk Group [Phase II]
Prazo: Assessed continuously during maintenance cycles 1-36 (cycle duration=4 weeks), up to 144 weeks + 30 days.
Maintenance SAE is any untoward medical occurrence at any dose during maintenance that: results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization (excluding planned hospitalizations), results in persistent or significant disability or incapacity (namely a substantial disruption of normal life functions), is a congenital anomaly or birth defect, or is considered a medically important event.
Assessed continuously during maintenance cycles 1-36 (cycle duration=4 weeks), up to 144 weeks + 30 days.
Induction Best Response by Age-Frailty Group [Phase II]
Prazo: Assessed day 1 of each cycle during induction cycles 1-8 (cycle duration=4 weeks), up to 32 weeks.
Best response over induction will be assessed according to the IMWG-URC including sCR, CR, VGPR, PR, MR, SD or PD.
Assessed day 1 of each cycle during induction cycles 1-8 (cycle duration=4 weeks), up to 32 weeks.
Maintenance Best Response by Age-Frailty Risk Group [Phase II]
Prazo: Assessed day 1 of each cycle during maintenance cycles 1-36 (cycle duration=4 weeks), up to 144 weeks.
Best response over maintenance will be assessed according to the IMWG-URC including sCR, CR, VGPR, PR, MR, SD or PD.
Assessed day 1 of each cycle during maintenance cycles 1-36 (cycle duration=4 weeks), up to 144 weeks.
Induction Minimal Residual Disease (MRD) Negativity Rate by Age-Frailty Group [Phase II]
Prazo: Assessed after induction cycle 8 (cycle duration=4 weeks), at 32 weeks.
Induction MRD-negative rate is defined as the proportion of participants achieving MRD negativity, as assessed by next-generation sequencing (NGS) or next-generation flow cytometry (NGF) with sensitivity of >1 in 10-5 nucleated cells, according to the IMWG-URC.
Assessed after induction cycle 8 (cycle duration=4 weeks), at 32 weeks.

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Cliford Mo, MD, Dana-Farber Cancer Institute

Publicações e links úteis

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Publicações Gerais

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)

3 de setembro de 2026

Conclusão Primária (Estimado)

1 de julho de 2029

Conclusão do estudo (Estimado)

1 de julho de 2034

Datas de inscrição no estudo

Enviado pela primeira vez

14 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

15 de maio de 2026

Primeira postagem (Real)

22 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

3 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de setembro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

The Harvard Cancer Center encourages and supports the responsible and ethical sharing of data from clinical trials. De-identified participant data from the final research dataset used in the published manuscript may only be shared under the terms of a Data Use Agreement. Requests may be directed to: [contact information for Sponsor Investigator or designee]. The protocol and statistical analysis plan will be made available on Clinicaltrials.gov only as required by federal regulation or as a condition of awards and agreements supporting the research.

Prazo de Compartilhamento de IPD

Data can be shared no earlier than 1 year following the date of publication

Critérios de acesso de compartilhamento IPD

Contact the Belfer office for Dana -Farber Innovations (BODFI) at innovations@dfci.harvard.edu

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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