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CM336 Plus Isatuximab for Newly Diagnosed Multiple Myeloma With Renal Impairment (CAREMM-012)

A Prospective, Single-arm, Single-center, Phase II Study of BCMA/CD3 Bispecific Antibody Combined With CD38 Monoclonal Antibody in Newly Diagnosed Multiple Myeloma Patients With Renal Impairment

This study is a single-center, single-arm, open-label, Phase II interventional clinical trial designed to evaluate the efficacy and safety of a CM336 and isatuximab regimen in patients with newly diagnosed multiple myeloma (NDMM) accompanied by renal impairment ([eGFR] < 40 mL/min). Enrolled subjects will receive three consecutive cycles of induction therapy with CM336 in combination with isatuximab.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

26

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

Luoghi di studio

      • Tianjin, Cina, 300000
        • Reclutamento
        • Institute of Hematology and Blood Diseases Hospital Chinese Academy of Medical Sciences
        • 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 to 80 years.
  2. Newly diagnosed symptomatic multiple myeloma (NDMM) according to the International Myeloma Working Group (IMWG) criteria. Patients who have received up to 1 cycle of prior anti-myeloma therapy are allowed to enroll.
  3. Presence of measurable disease at diagnosis, meeting at least one of the following criteria:

    A.Serum M-protein ≥ 1 g/dL (> 10 g/L) measured by serum protein electrophoresis (SPEP) (for IgA or IgD myeloma, quantitative IgA or IgD levels may be used instead); OR

    B.Urine M-protein ≥ 200 mg/24 hours; OR

    C.If both serum and urine M-protein do not meet the above criteria, an abnormal serum free light chain (FLC) ratio (normal FLC ratio: 0.26 to 1.65) with an involved serum FLC level ≥ 100 mg/L.

  4. Accompanied by myeloma-related renal impairment (RI), defined as an estimated glomerular filtration rate (eGFR) < 40 mL/min (calculated using the Modification of Diet in Renal Disease [MDRD] formula). The type of renal impairment must be restricted to cast nephropathy, which can be confirmed by renal biopsy or by the investigator's clinical judgment based on light chain proteinuria. If urine albumin accounts for more than 30% of the total urine protein, a renal biopsy is mandatory to confirm cast nephropathy.
  5. Eastern Cooperative Oncology Group (ECOG) performance status score of ≤ 2.
  6. Adequate major organ function, meeting the following criteria:

    A. Hematological function:

    1. Absolute neutrophil count (ANC) ≥ 1.0 × 10^9/L, and without receiving granulocyte colony-stimulating factor (G-CSF) or granulocyte-macrophage colony-stimulating factor (GM-CSF) within 7 days, or pegylated G-CSF within 14 days prior to testing;
    2. Hemoglobin ≥ 60 g/L, and without receiving whole blood or red blood cell transfusions within 7 days prior to testing;
    3. Platelet count ≥ 50 × 10^9/L, and without receiving whole blood, platelet transfusions, or thrombopoietin receptor agonists (TPO-RAs) within 7 days prior to testing.

    B. Hepatic function:

    Alanine aminotransferase (ALT) ≤ 3 × upper limit of normal (ULN), aspartate aminotransferase (AST) ≤ 3 × ULN, and total bilirubin ≤ 2 × ULN (subjects with a history of Gilbert's syndrome are eligible if direct bilirubin ≤ 2.0 × ULN).

    C. Coagulation function:

  7. International Normalized Ratio (INR) or Activated Partial Thromboplastin Time (APTT) ≤ 1.5 × ULN.
  8. No active concomitant malignancies or malignancies with an expected survival of less than 12 months.
  9. Willingness to participate in the study, good compliance, and ability to sign the informed consent form (ICF).

Exclusion Criteria:

  1. Diagnosis of smoldering multiple myeloma (SMM), monoclonal gammopathy of undetermined significance (MGUS), Waldenström's macroglobulinemia, polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome, amyloidosis, or secondary plasma cell leukemia.
  2. Central nervous system (CNS) involvement or clinical evidence of meningeal involvement.
  3. Severe and/or uncontrolled cardiac diseases, including: unstable angina, symptomatic congestive heart failure, myocardial infarction within 6 months prior to enrollment, severe and uncontrolled arrhythmias; or other cardiovascular/cerebrovascular diseases deemed unsuitable for study participation by the investigator.
  4. Presence of active infections, including: HIV positive; active Hepatitis B (HBV-DNA positive); active Hepatitis C (HCV-RNA positive); active or latent syphilis infection (Treponema pallidum antibody positive); active tuberculosis (active TB infection indicated by chest imaging or other relevant tests within the past 3 months or during the screening period); or other active infections deemed unsuitable for study participation by the investigator.
  5. Patients with concurrent malignancies; or severe concomitant diseases that, in the investigator's judgment, would severely compromise patient safety or interfere with study completion.
  6. Pregnant or lactating women.
  7. History of severe allergic reactions (Grade ≥ 3) or hypersensitivity to any components of the study drugs.
  8. Unable or unwilling to sign the informed consent form.
  9. Any other conditions that, in the opinion of the investigator, make the patient unsuitable for enrollment.

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: CM336 plus Isatuximab
Enrolled patients will receive 3 cycles of induction therapy with CM336 in combination with isatuximab.

CM336: Administered subcutaneously (SC) via a step-up dosing regimen, which includes a step-up dosing phase and a target dosing phase. Upon reaching the target dose, it will be administered once weekly.

Isatuximab: Administered intravenously (IV) at a dose of 10 mg/kg, given weekly during Cycle 1, and every two weeks during Cycles 2 and 3.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Overall Renal Response Rate (Minor Response or better)
Lasso di tempo: At the end of Cycle 3 (each cycle is 28 days)
The Overall Renal Response Rate is defined as the percentage of participants who achieve a renal response of Minor Response or better (including Minor Response, Partial Response, and Complete Response) according to the International Myeloma Working Group (IMWG) criteria for renal impairment.
At the end of Cycle 3 (each cycle is 28 days)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Hematological Overall Response Rate (ORR)
Lasso di tempo: From the first dose of CM336 through 30 days after the last dose of CM336
The percentage of participants who achieve a hematological response of Partial Response (PR) or better (including PR, Very Good Partial Response [VGPR], Complete Response [CR], and Stringent Complete Response [sCR]) according to the International Myeloma Working Group (IMWG) uniform response criteria.
From the first dose of CM336 through 30 days after the last dose of CM336
MRD Negativity Rate
Lasso di tempo: At the end of Cycle 3 (each cycle is 28 days)
The percentage of participants who achieve MRD negativity in the bone marrow. MRD negativity is defined by a threshold of 10^-5, assessed via Next-Generation Flow (NGF) cytometry in accordance with IMWG criteria.
At the end of Cycle 3 (each cycle is 28 days)
Kinetics of Serum Free Light Chain (sFLC) Reduction
Lasso di tempo: From the first dose of CM336 through 30 days after the last dose of CM336
The rate and time to achieve a specific percentage or absolute reduction in involved serum free light chain (sFLC) levels from baseline.
From the first dose of CM336 through 30 days after the last dose of CM336
Incidence and Severity of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Lasso di tempo: From the first dose of CM336 through 30 days after the last dose of CM336.
Safety will be assessed by monitoring the incidence, nature, and severity of treatment-emergent adverse events (TEAEs), including serious adverse events (SAEs), adverse events of special interest (AESIs) such as cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS), graded according to NCI CTCAE v5.0 and ASTCT criteria. Dose interruptions, modifications, or discontinuations due to toxicity will also be recorded.
From the first dose of CM336 through 30 days after the last dose of CM336.
PFS
Lasso di tempo: From the first dose of CM336 up to the date of first documented disease progression or death, up to approximately 24 months.
The time from the start of the study treatment to the date of first documented disease progression (according to IMWG criteria) or death from any cause, whichever occurs first.
From the first dose of CM336 up to the date of first documented disease progression or death, up to approximately 24 months.
OS
Lasso di tempo: From the first dose of CM336 up to the date of death from any cause, up to approximately 24 months.
The time from the start of the study treatment to the date of death from any cause.
From the first dose of CM336 up to the date of death from any cause, up to approximately 24 months.
Rate of Renal Partial Response or Better
Lasso di tempo: At the end of Cycle 3 (each cycle is 28 days)
Rate of renal partial response or better is defined as the percentage of participants who achieve a renal response of Partial Response or better (including Partial Response and Complete Response) according to the International Myeloma Working Group (IMWG) criteria for renal impairment.
At the end of Cycle 3 (each cycle is 28 days)

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)

10 settembre 2026

Completamento primario (Stimato)

1 maggio 2028

Completamento dello studio (Stimato)

30 dicembre 2028

Date di iscrizione allo studio

Primo inviato

13 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

10 maggio 2026

Primo Inserito (Effettivo)

14 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

17 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

15 settembre 2026

Ultimo verificato

1 agosto 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)?

INDECISO

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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