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Nemtabrutinib for Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Leukemia (SLL) Refractory to Covalent Bruton Tyrosine Kinase Inhibitor or Pirtobrutinib and Previously Treated With a BCL2 Inhibitor

Background:

Chronic lymphocytic leukemia (CLL)/small lymphocytic leukemia (SLL) are diseases in which the body makes too many white blood cells that do not work properly. Because white cells play a role in immune function, people with CLL/SLL may be at greater risk of infections. CLL/SLL can be controlled with drugs, but many people develop resistance, and the treatments stop working.

Objective:

To test a new drug (nemtabrutinib) in people with CLL/SLL.

Eligibility:

People aged 18 years or older with CLL/SLL that persists despite treatment.

Design:

Participants will be screened. They will have imaging scans, blood and urine tests, and a test of their heart function. They will have a bone marrow biopsy: a sample of tissue and fluids will be drawn from inside their hip bone. They may also have a sample cut from a swollen lymph node, if one is safe to access.

Nemtabrutinib is a tablet taken by mouth. Participants will take the drug once a day at home in 4-week cycles. They will have clinic visits at least every 4 weeks for the first 6 months and then every 3 months after that.

Biopsies, imaging exams, and other tests may be repeated at these visits. Participants may also undergo lymphapheresis: Blood will be drawn from a tube inserted into a vein. The blood will pass through a machine that separates out cancer and immune cells. The remaining blood will be returned to the body through a different tube.

Participants may stay in the study as long as the drug is helping them.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Study Description:

This is a phase 2 study of nemtabrutinib for chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) refractory to treatment with covalent Bruton tyrosine kinase inhibitor (BTKi) or pirtobrutinib, and previously treated with B-cell lymphoma 2 inhibitor (BCL2i). Subjects will be treated with nemtabrutinib 65 mg by mouth once daily until disease progression or toxicity. Efficacy will be evaluated separately in CLL/SLL refractory to covalent BTKi (cBTKi) and in CLL/SLL refractory to pirtobrutinib. Efficacy will also be evaluated in molecular subgroups based on BTK and PLCG2 mutations, IGHV mutational status, and cytogenetic abnormalities. The pharmacodynamic effects of nemtabrutinib on tumor and immune cells will be assessed in peripheral blood, lymph node, and bone marrow. Clonal shifts during treatment with nemtabrutinib will be described.

For the purposes of this protocol, the term "CLL" will be used throughout to refer collectively to chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL), unless otherwise specified.

Objectives:

Primary Objectives:

  • Evaluate the efficacy of nemtabrutinib in CLL refractory to cBTKi and previously treated with BCL2i
  • Evaluate the efficacy of nemtabrutinib in CLL refractory to pirtobrutinib and previously treated with BCL2i

Secondary Objectives:

  • Evaluate the efficacy of nemtabrutinib in CLL with and without BTK and PLCG2 mutations
  • Evaluate the efficacy of nemtabrutinib in CLL prognostic risk groups

Exploratory Objectives:

  • Characterize the pharmacodynamic effects of nemtabrutinib on tumor and immune cells
  • Understand clonal shifts during treatment with nemtabrutinib
  • Identify potential biomarkers predictive of response to nemtabrutinib

Endpoints:

Primary Endpoints:

  • Overall response rate (ORR) to nemtabrutinib in CLL refractory to cBTKi and previously treated with BCL2i
  • ORR to nemtabrutinib in CLL refractory to pirtobrutinib and previously treated with BCL2i

Secondary Endpoints:

  • Progression-free survival (PFS) and time to response (TTR) during treatment with nemtabrutinib in CLL refractory to cBTKi and previously treated with BCL2i
  • PFS and TTR during treatment with nemtabrutinib in CLL refractory to pirtobrutinib and previously treated with BCL2i
  • ORR, PFS, and TTR in BTK and PLCG2 wild-type and mutated CLL
  • ORR, PFS, and TTR based on IGHV mutational status and cytogenetic abnormalities

Exploratory Endpoints:

  • Gene expression profiling in tumor and immune cells from peripheral blood, lymph node, and bone marrow during treatment with nemtabrutinib
  • Targeted or whole genome/exome sequencing of tumor cells during treatment with nemtabrutinib
  • Association between ORR, PFS, and potential biomarkers (e.g., molecular, serum)
  • Overall survival (OS) during treatment with nemtabrutinib in CLL refractory to cBTKi and previously treated with BCL2i
  • OS during treatment with nemtabrutinib in CLL refractory to pirtobrutinib and previously treated with BCL2i

Tipo di studio

Interventistico

Iscrizione (Stimato)

32

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

    • Maryland
      • Bethesda, Maryland, Stati Uniti, 20892
        • National Institutes of Health Clinical Center
        • Contatto:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • Numero di telefono: TTY dial 711 800-411-1222
          • Email: ccopr@nih.gov

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

Da 18 anni a 100 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

  • INCLUSION CRITERIA:

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

  1. Age >=18 years. CLL/SLL is extremely rare in patients < 18 years old.

  2. Ability to comprehend the investigational nature of the study and provide informed consent

  3. Confirmed diagnosis of CLL or SLL according to International Workshop on CLL (iwCLL) guidelines

    1. Coexpression of CD5, CD19, CD20, and CD23 expression and light-chain restriction
    2. CLL: clonal B-lymphocytosis >=5,000 cells/mL OR SLL: lymphadenopathy with the tissue morphology of CLL but that are not leukemic, <5,000 cells/mL
  4. Cohort A: refractoriness to cBTKi defined as lack of response or progressive disease while on therapy

    Cohort B: refractoriness to pirtobrutinib defined as lack of response or progressive disease while on therapy

  5. Prior treatment with a BCL2i

  6. Active disease requiring treatment or progressive disease during or after therapy according to iwCLL guidelines

  7. Measurable disease characterized by >=1 of the following:

    1. Lymphadenopathy: >=1 lymph node measuring >=1.5 cm in the greatest diameter
    2. Splenomegaly: spleen measuring >13 cm in craniocaudal length
    3. Lymphocytosis: >=5,000 B cells/microL
    4. Bone marrow infiltration: CLL comprising >=30% of all cells
  8. A female participant is eligible to participate if not pregnant or breastfeeding, and >=1 of the following conditions applies:

    Is not a person of childbearing potential (POCBP)

    OR

    Is a POCBP and

    • Uses a contraceptive method
    • Has a negative highly sensitive serum pregnancy test within 7 days before the first dose of study intervention.
  9. The participant has provided documented informed consent for the trial.

  10. Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2 within 7 days prior to the first dose of study intervention.

  11. The ability to swallow and retain oral medication

    Note: Administration of nemtabrutinib is not permitted through a PEG-J tube.

  12. Participants who are HBsAg positive are eligible if they have received HBV antiviral therapy for >=4 weeks and have undetectable HBV viral load prior to study entry.

    Note: Participants should remain on anti-viral therapy throughout study intervention and follow local guidelines for HBV anti-viral therapy post completion of study intervention. Hepatitis B screening tests should include HBsAg, HBcAb, HBsAb . Hepatitis B screening tests are not required unless:

    • Known history of HBV infection
    • As mandated by local health authority
  13. Participants with history of HCV infection are eligible if HCV viral load is undetectable at screening.

    Note: Participants must have completed curative anti-viral therapy >=4 weeks prior to nemtabrutinib initiation.

  14. Participants with HIV are eligible if they meet ALL of the following criteria:

    • The CD4 count is >350 cells/microL at screening
    • The HIV viral load is below the detectable level as per locally available testing
    • Are on a stable ART regimen for >=4 weeks prior to study entry

    Note: ART includes drugs, which are NOT strong CYP3A4 inducers (participants receiving ART that are strong CYP3A4 inducers are not eligible to be included in the study).

    • Are compliant with their ART

    Note: If the participant has had an AIDS defining opportunistic infection in the past 12 months prior to screening, they are not eligible to be included in the study.

  15. Adequate organ function as defined in the following table. Specimens must be collected within 7 days prior to drug initiation.

Organ Function Laboratory Values:

  • Hematological

    --Absolute neutrophil count (ANC) >=750/microL (or >=500/mircoL in participants with documented bone marrow involvement)*

    • Platelets >=50,000/mircoL*
    • Hemoglobin >=8 g/dL*
  • Renal

    • Creatinine <=1.5 x ULN OR Measured or calculated creatinine clearance (GFR can also be used in place of creatinine or CrCl) >=30 mL/min for participant with creatinine levels >1.5 x institutional ULN
  • Hepatic

    • Total bilirubin <=1.5 x ULN OR direct bilirubin <= ULN for participants with total bilirubin levels >1.5 x ULN
    • AST (SGOT) and ALT (SGPT) <=2.5 x ULN
  • Coagulation

    • PT, aPTT <=1.5 x ULN unless participant is receiving anticoagulant therapy

ALT (SGPT)=alanine aminotransferase (serum glutamic pyruvic transaminase);

AST (SGOT)=aspartate aminotransferase (serum glutamic oxaloacetic transaminase);

ULN=upper limit of normal; INR=international normalized ratio; PT=prothrombin time; aPTT=activated partial thromboplastin time

*Growth factor and/or transfusion support is permissible to meet this requirement if cytopenia is due to bone marrow involvement of CLL

EXCLUSION CRITERIA:

The participant must be excluded from the study if the participant meets any of the following criteria:

  1. Documented CNS involvement

  2. Active HBV/HCV infection. See Inclusion Criteria 10 (HBV) and 11 (HCV) for requirements.

  3. Known active cytomegalovirus (CMV) infection. Unknown or negative status are eligible.

  4. Gastrointestinal dysfunction that may affect drug absorption (e.g., gastric bypass surgery, gastrectomy).

  5. Active, uncontrolled infection requiring systemic therapy, including IV antibiotics during screening. Participants may be rescreened followed completion of IV antibiotic course.

  6. Stroke or intracranial hemorrhage within 6 months of screening

  7. Hypertensive urgency or emergency

  8. Active, clinically significant cardiovascular disease including:

    • Uncontrolled or symptomatic arrhythmias
    • Class 3 or 4 congestive heart failure as defined by New York Heart Association Functional Classification
    • Myocardial infarction, unstable angina or acute coronary syndrome within 6 months of screening.
    • History of Mobitz II second-degree or third-degree heart block without a permanent pacemaker in place.
  9. QTcF >450 milliseconds based on Fridericia s formula (NOTE: QTcF value may be calculated as the numerical average of up to 3 separate readings for eligibility).

  10. Known allergy/sensitivity to nemtabrutinib or any of the excipients (hypromellose acetate succinate, microcrystalline cellulose, mannitol, croscarmellose sodium, magnesium stearate, and may include film coat).

  11. History of severe bleeding disorders defined as an ongoing congenital or acquired condition that leads to an increased likelihood of bleeding.

  12. Known additional malignancy that is progressing or has required active treatment within the past 2 years.

    Note: Participants with basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or carcinoma in situ, excluding carcinoma in situ of the bladder, that have undergone potentially curative therapy are not excluded. Participants with low-risk, early-stage prostate cancer (T1-T2a, Gleason score <=6, and PSA <10 ng/mL), either treated with definitive intent or untreated in active surveillance with stable disease, are not excluded.

  13. Currently being treated with the following drugs:

    • P-gp substrates with a narrow therapeutic index
    • CYP3A strong inducers
    • CYP3A strong inhibitors

    Note: A washout period of at least 5 times the half-life after the last dose of any of the above treatments is required for a participant to be eligible for study enrollment.

  14. Has received prior systemic anti-CLL therapy within 3 half-lives or 4 weeks (if prior therapy was a monoclonal antibody) of start of nemtabrutinib.

  15. Has received prior radiotherapy within 2 weeks of start of nemtabrutinib or radiation-related toxicities requiring corticosteroids.

    Note: Two weeks or fewer of palliative radiotherapy for non-CNS disease, with a 1-week washout, is permitted.

  16. Has received a live vaccine or live-attenuated vaccine within 30 days before the first dose of nemtabrutinib. Administration of killed vaccines are allowed.

  17. Patients requiring ongoing treatment with warfarin within 7 days of start of nemtabrutinib

  18. Enrolled on another therapeutic clinical trial for CLL/SLL at the start of nemtabrutinib. Concurrent enrollment on another therapeutic clinical trial or any trial designed to impact the efficacy of anticancer therapy is prohibited.

  19. Has active autoimmune disease that has required systemic treatment in the past 2 years except replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid)

  20. Has not adequately recovered after 4 weeks from major surgery or has ongoing surgical complications.

    Note: Biopsy and placement of central venous access devices are not considered major surgery.

  21. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.

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: Treatment

Nemtabrutinib 65 mg will be given orally once daily in 28-day cycles.

Nemtabrutinib 65 mg will be given orally once daily in 28-day cycles and continue treatment until disease progression, unacceptable toxicity, or another discontinuation criterion is met.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Overall response rate (ORR)
Lasso di tempo: After 6 cycles of nemtabrutinib

ORR is defined as the proportion of subjects who achieve partial response (PR) or better, including partial response with lymphocytosis (PRL), as their best response. ORR will be evaluated separately in each cohort:CLL/SLL refractory to covalent BTK inhibitor (cBTKi) and previously treated with a BCL2 inhibitor and CLL/SLL refractory to pirtobrutinib and previously treated with a BCL2 inhibitor.

After 6 cycles of nemtabrutinib

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Progression-free survival (PFS) and time to response (TTR)
Lasso di tempo: PFS - time of disease progression or death from any cause; TTR - time to partial remission or better

Progression-free survival (PFS) and time to response (TTR) during treatment with nemtabrutinib will be evaluated separately in each cohort: CLL/SLL refractory to covalent BTK inhibitor (cBTKi) and previously treated with a BCL2 inhibitor and CLL/SLL refractory to pirtobrutinib and previously treated with a BCL2 inhibitor

PFS - time of disease progression or death from any cause; TTR - time to partial remission or better
ORR, PFS, and TTR in BTK and PLCG2 wild-type and mutated CLL
Lasso di tempo: PFS - time to first sign of disease progression or death; TTR - time to partial remission or better; ORR - after 6 cycles with ongoing assessments.

PFS is measured from the first day of treatment until the first sign of disease progression or death from any cause. TTR is measured from the first day of treatment until the first occurrence of partial remission or better. Response-based endpoints (including ORR) are evaluated after 6 cycles for the primary response assessment, with ongoing assessments during treatment and follow-up as specified in the schedule of activities.

PFS - time to first sign of disease progression or death; TTR - time to partial remission or better; ORR - after 6 cycles with ongoing assessments.
ORR, PFS, and TTR based on IGHV mutational status and cytogenetic abnormalities
Lasso di tempo: PFS - time to first sign of disease progression or death; TTR - time to partial remission or better; ORR - after 6 cycles with ongoing assessments.

PFS is measured from the first day of treatment until the first sign of disease progression or death from any cause. TTR is measured from the first day of treatment until the first occurrence of partial remission or better. Response-based endpoints (including ORR) are evaluated after 6 cycles for the primary response assessment, with ongoing assessments during treatment and follow-up as specified in the schedule of activities.

PFS - time to first sign of disease progression or death; TTR - time to partial remission or better; ORR - after 6 cycles with ongoing assessments.

Collaboratori e investigatori

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

Sponsor

Investigatori

  • Investigatore principale: Laura S Samples, M.D., National Heart, Lung, and Blood Institute (NHLBI)

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.

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)

9 novembre 2026

Completamento primario (Stimato)

1 dicembre 2030

Completamento dello studio (Stimato)

1 dicembre 2031

Date di iscrizione allo studio

Primo inviato

29 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

31 agosto 2026

Primo Inserito (Effettivo)

1 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

4 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 novembre 2026

Ultimo verificato

26 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 10002165
  • 002165-H

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

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 .