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S243249 Monotherapy in Patients With Relapsed or Refractory Acute Leukemia With a KMT2A or NUP98 Translocation or Relapsed or Refractory AML With NPM1c Mutation

2026年9月2日 更新者:Servier

A Phase 1/2, Dose Optimization and Dose Expansion, Multicenter, Open-label Study to Evaluate the Safety, Pharmacokinetics, and Efficacy of Menin Inhibitor S243249 Monotherapy in Patients With Relapsed or Refractory Acute Leukemia With a KMT2A or NUP98 Translocation or Patients With Relapsed or Refractory Acute Myeloid Leukemia With NPM1c Mutation

The objective of this study is to establish the efficacy, safety, and tolerability of S243249 and to establish the recommended phase 2 dose (RP2D) of S243249 monotherapy in participants with relapsed/refractory (R/R) acute leukemia with select mutations. Phase 1 dose optimization will determine the RP2D to be used in Phase 2 dose expansion. The study will include a screening period, a treatment period consisting of continuous 28-day cycles of treatment, a safety follow-up period and a long-term follow-up period. Participants may undergo blood tests, electrocardiogram (ECG), bone marrow aspirations, vital sign checks, questionnaires, and physical exams.

調査の概要

研究の種類

介入

入学 (推定)

80

段階

  • フェーズ2
  • フェーズ 1

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

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Aged ≥ 18 years old.
  • Negative serum pregnancy (β-hCG) test in women of childbearing potential at screening
  • Cytomorphology-confirmed diagnosis of R/R acute leukemia (including AML, ALL, and mixed lineage leukemia) according to the WHO criteria in 2022. R/R acute leukemia must meet at least one of the following conditions:
  • Primary refractory disease, defined as non-response to 2 courses of standard induction therapy.
  • R/R disease, defined as > 5% blasts on bone marrow aspirate (BMA) / bone marrow biopsy (BMB) after completing prior therapy.
  • Relapse after allogeneic hematopoietic stem cell transplantation (HSCT), autologous HSCT, or immunotherapy such as chimeric antigen receptor T cell therapy (CAR-T) and T cell engager (TCE).
  • Participants with secondary AML or AML transformed from myelodysplastic syndrome (MDS), myeloproliferative neoplasm (MPN), etc., can be included in the study, if they meet the above criteria after the disease has transformed into AML.
  • Confirmation of KMT2At, NUP98t, or NPM1c mutation using next generation sequencing (NGS), fluorescence in situ hybridization (FISH), or polymerase chain reaction (PCR) based test in an accredited local or central lab within 28 days before start of treatment.
  • Peripheral blood white blood cell (WBC) count ≤ 25 mm3 (hydroxyurea, steroids, or vincristine to reduce peripheral WBC count is permitted).
  • Participants will be at least 2 weeks from prior therapy (except hydroxyurea, vincristine, or steroids and prespecified prephase therapy) and recovered from nadir to no worse than Grade 1 nonhematological toxicity from the prior treatment.
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2.
  • Adequate electrolytes, liver, kidney, and cardiac function
  • Sexually active male or female participants of childbearing potential must agree to use 2 medically accepted forms of effective contraception, e.g., oral, parenteral, or implanted contraceptives; intrauterine devices; and barrier methods with spermicides, during the study and for 3 or 6 months after the final administration of investigational medicinal product (IMP), in males and females respectively. Egg donation is not allowed during the study or within 6 months of the last dose of S243249.
  • Male participants with women of childbearing potential (WOCBP) partners must use a condom during the study and for at least 3 months after the final administration of IMP.

Exclusion Criteria:

  • Active central nervous system (CNS) leukemia (including imaging abnormalities and cerebrospinal fluid (CSF) smear or flow cytometry indicating leukemia cells)).
  • Active disseminated intravascular coagulation (DIC).
  • Active uncontrolled infection (prophylaxis because of absolute neutrophil count [ANC] is excepted).
  • Diagnosis of acute promyelocytic leukemia (APL, M3).
  • Corrected QT interval calculated by Fridericia (QTcF) > 450 msec on screening ECG.
  • Participants with an increased pro-arrhythmic risk such as those with congenital long QT syndrome.
  • Uncontrolled or severe cardiovascular disease, , within 12 months.
  • Uncontrolled serious arrhythmias.
  • Clinically significant pericardial disease.
  • History of other malignancy within the past 5 years.
  • Participants who receive autologous hematopoietic stem cell transplantation (ASCT) or CAR-T therapy within 60 days of the first dose of S243249 or have not yet recovered from toxicity related to ASCT or CAR-T therapy.
  • Participants who receive allogeneic HSCT within 100 days of the first dose of S243249, still have active acute or chronic graft versus host disease (GVHD), or still require immune-modulating therapy.
  • Have an active infection of hepatitis B or hepatitis C.
  • Have advanced liver disease or cirrhosis.
  • Uncontrolled human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome related illness.
  • Pregnant and/or breast-feeding (lactating) women.
  • Participant has received anti-leukemia treatment, including chemotherapy, radiation therapy, targeted small molecule agents, biologic agents, immunotherapy, or any other investigational therapy (excluding hydroxyurea, or vincristine for cytoreduction) within 2 weeks prior to the first dose of S243249.
  • Previous treatment targeting menin, dose optimization phase only.
  • Any concomitant participation in another therapeutic clinical trial is prohibited. Any participation in another nontherapeutic clinical trial could be approved by the medical monitor.
  • Participants taking medications known to prolong the QT/QTc interval (with the exception of necessary azole antifungals).
  • Ongoing toxicity from prior anti-leukemia therapy that has not resolved to Grade 1 7 days prior to the first dose of S243249 has to be approved by the medical monitor.
  • Uncontrolled active infection
  • Known allergy or hypersensitivity to menin inhibitors or any component of S243249.

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:ランダム化
  • 介入モデル:並列代入
  • 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:Phase 1 Dose Optimization: Cohort 1
For participants without strong CYP3A4 inhibitors
Taken twice daily by mouth
実験的:Phase 1 Dose Optimization: Cohort 2
For participants without strong CYP3A4 inhibitors
Taken twice daily by mouth
実験的:Phase 1 Dose Optimization: Cohort 3
For participants with strong CYP3A4 inhibitors
Taken twice daily by mouth
実験的:Phase 1 Dose Optimization: Cohort 4
For participants with strong CYP3A4 inhibitors
Taken twice daily by mouth

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
時間枠
Incidence of Adverse Events (AEs)
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Severity of AEs
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of changes in laboratory values
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of changes in electrocardiogram (ECG)
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of changes in vital signs
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of AEs leading to dose interruption
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of AEs leading to dose modification
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of AEs leading to dose delays
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of AEs leading to permanent treatment discontinuation
時間枠:Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Complete remission (CR) + Complete remission with partial recovery of hematology (CRh) rate
時間枠:Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)

二次結果の測定

結果測定
メジャーの説明
時間枠
Overall response rate (ORR)
時間枠:Through Long-term Follow-up (Approximately 5 years)
CR + CRh + Complete remission with incomplete hematological recovery (CRi) + Morphologically leukemic state (MLFS) + Partial remission (PR)
Through Long-term Follow-up (Approximately 5 years)
Composite complete remission (CRc) rate
時間枠:Through Long-term Follow-up (Approximately 5 years)
CRc is CR + CRh + CRi
Through Long-term Follow-up (Approximately 5 years)
CR rate
時間枠:Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Rate of CR/CRh Minimal residual disease (MRD) negativity
時間枠:Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Duration of response (DOR)
時間枠:Through Long-term Follow-up (Approximately 5 years)
Measured from the date of first achievement of CR/CRh, CR, CR/CRh MRD negativity, CRc and ORR until hematologic relapse or death from any cause
Through Long-term Follow-up (Approximately 5 years)
Time to response (TTR)
時間枠:Through Long-term Follow-up (Approximately 5 years)
Measured from the date of first dose administration until the first achievement of CR/CRh, CR, CR/CRh MRD negativity, CRc and ORR
Through Long-term Follow-up (Approximately 5 years)
Transfusion independence 56 days (TI-56)
時間枠:Through Long-term Follow-up (Approximately 5 years)
The absence of red blood cells and platelet transfusions lasting for 56 consecutive days during which the patient is either on Investigational medicinal product (IMP) or following discontinuation from IMP but before the start of new therapy.
Through Long-term Follow-up (Approximately 5 years)
Transfusion independence 112 days (TI-112)
時間枠:Through Long-term Follow-up (Approximately 5 years)
The absence of red blood cells and platelet transfusions lasting for 112 consecutive days during which the patient is either on IMP or following discontinuation from IMP but before the start of new therapy.
Through Long-term Follow-up (Approximately 5 years)
Event free survival (EFS)
時間枠:Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Cumulative relapse rate (CIR)
時間枠:Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Cumulative mortality (CID)
時間枠:Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Overall survival (OS)
時間枠:Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Quality of Life (QoL) measured via EuroQol 5-Dimension 5-Level questionnaire (EQ-5D-5L)
時間枠:Through Safety Follow-up (Approximately 3 years)
EQ-5D-5L scores range from 0-5 with 5 representing the best QoL.
Through Safety Follow-up (Approximately 3 years)
QoL measured via Hematological malignancy specific patient-reported outcome (HM-PRO)
時間枠:Through Safety Follow-up (Approximately 3 years)
HM-PRO Part A scores range from 0 to 48 and Part B scores from 0 to 36, with a higher score representing the largest impact on quality of life.
Through Safety Follow-up (Approximately 3 years)
Health economic outcomes measured via EQ-5D-5L
時間枠:Through Safety Follow-up (Approximately 3 years)
EQ-5D-5L scores range from 0-1 with 1 representing the best health economic outcomes.
Through Safety Follow-up (Approximately 3 years)
Health economic outcomes measured via HM-PRO
時間枠:Through Safety Follow-up (Approximately 3 years)
HM-PRO scores range from 0 to 48, with a higher score representing the largest impact on health economic outcomes.
Through Safety Follow-up (Approximately 3 years)
Ability to proceed to hematopoietic stem cell transplantation (HSCT) as assessed by the investigator
時間枠:Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Plasma concentration of S243249 and relevant metabolites
時間枠:Through Cycle 6 Day 1 (each cycle is 28 days)
Plasma samples will be analyzed to determine concentrations of S243249 and relevant metabolites
Through Cycle 6 Day 1 (each cycle is 28 days)
Tmax
時間枠:Through Cycle 6 Day 1 (each cycle is 28 days)
Time to observed maximum plasma concentration of S243249 and relevant metabolites
Through Cycle 6 Day 1 (each cycle is 28 days)
Cmax
時間枠:Through Cycle 6 Day 1 (each cycle is 28 days)
Maximum plasma concentration of S243249 and relevant metabolites
Through Cycle 6 Day 1 (each cycle is 28 days)
AUC0-t
時間枠:Through Cycle 6 Day 1 (each cycle is 28 days)
Area under the plasma concentration-time curve from time 0 to time t of S243249 and relevant metabolites
Through Cycle 6 Day 1 (each cycle is 28 days)

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。

スポンサー

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10月20日

一次修了 (推定)

2029年8月11日

研究の完了 (推定)

2030年8月25日

試験登録日

最初に提出

2026年7月13日

QC基準を満たした最初の提出物

2026年7月22日

最初の投稿 (実際)

2026年7月23日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月3日

QC基準を満たした最後の更新が送信されました

2026年9月2日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • BN104-102
  • 2025 (米国 NIH グラント/契約:Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
  • 2025-524689-74-00 (Ctis)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

Qualified scientific and medical researchers can request access to anonymized patient-level and study-level clinical trial data.

Access can be requested for all interventional clinical studies:

  • used for Marketing Authorization (MA) of medicines and new indications approved after 1 January 2014 in the European Economic Area (EEA) or the United States (US).
  • where Servier is the Marketing Authorization Holder (MAH). The date of the first MA of the new medicine (or the new indication) in one of the EEA Member States will be considered for this scope.

In addition, access can be requested for all interventional clinical studies in patients:

  • sponsored by Servier
  • with a first patient enrolled as of 1 January 2004 onwards for New Chemical Entity or New Biological Entity (new pharmaceutical form excluded) for which development has been terminated before any Marketing authorization (MA) approval.

IPD 共有時間枠

After Marketing Authorization in EEA or US if the study is used for the approval.

IPD 共有アクセス基準

Researchers should register on Servier Data Portal and fill in the research proposal form. This form in four parts should be fully documented. The Research Proposal Form will not be reviewed until all mandatory fields are completed.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

はい

米国FDA規制機器製品の研究

いいえ

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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