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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.

調査の概要

状態

まだ募集していません

介入・治療

詳細な説明

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

研究の種類

介入

入学 (推定)

32

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Maryland
      • Bethesda、Maryland、アメリカ、20892
        • National Institutes of Health Clinical Center
        • コンタクト:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • 電話番号:TTY dial 711 800-411-1222
          • メール:ccopr@nih.gov

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~100年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

  • 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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Overall response rate (ORR)
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Progression-free survival (PFS) and time to response (TTR)
時間枠: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
時間枠: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
時間枠: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.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Laura S Samples, M.D.、National Heart, Lung, and Blood Institute (NHLBI)

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年11月9日

一次修了 (推定)

2030年12月1日

研究の完了 (推定)

2031年12月1日

試験登録日

最初に提出

2026年8月29日

QC基準を満たした最初の提出物

2026年8月31日

最初の投稿 (実際)

2026年9月1日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月4日

QC基準を満たした最後の更新が送信されました

2026年11月3日

最終確認日

2026年10月26日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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