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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

2. September 2026 aktualisiert von: 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.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

80

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Phase 1 Dose Optimization: Cohort 1
For participants without strong CYP3A4 inhibitors
Taken twice daily by mouth
Experimental: Phase 1 Dose Optimization: Cohort 2
For participants without strong CYP3A4 inhibitors
Taken twice daily by mouth
Experimental: Phase 1 Dose Optimization: Cohort 3
For participants with strong CYP3A4 inhibitors
Taken twice daily by mouth
Experimental: Phase 1 Dose Optimization: Cohort 4
For participants with strong CYP3A4 inhibitors
Taken twice daily by mouth

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Incidence of Adverse Events (AEs)
Zeitfenster: Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Severity of AEs
Zeitfenster: Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of changes in laboratory values
Zeitfenster: Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of changes in electrocardiogram (ECG)
Zeitfenster: Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of changes in vital signs
Zeitfenster: Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of AEs leading to dose interruption
Zeitfenster: Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of AEs leading to dose modification
Zeitfenster: Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of AEs leading to dose delays
Zeitfenster: Through Safety Follow-up (Approximately 3 years)
Through Safety Follow-up (Approximately 3 years)
Number of AEs leading to permanent treatment discontinuation
Zeitfenster: 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
Zeitfenster: Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Overall response rate (ORR)
Zeitfenster: 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
Zeitfenster: Through Long-term Follow-up (Approximately 5 years)
CRc is CR + CRh + CRi
Through Long-term Follow-up (Approximately 5 years)
CR rate
Zeitfenster: 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
Zeitfenster: Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Duration of response (DOR)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Cumulative relapse rate (CIR)
Zeitfenster: Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Cumulative mortality (CID)
Zeitfenster: Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Overall survival (OS)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: Through Long-term Follow-up (Approximately 5 years)
Through Long-term Follow-up (Approximately 5 years)
Plasma concentration of S243249 and relevant metabolites
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

20. Oktober 2026

Primärer Abschluss (Geschätzt)

11. August 2029

Studienabschluss (Geschätzt)

25. August 2030

Studienanmeldedaten

Zuerst eingereicht

13. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

22. Juli 2026

Zuerst gepostet (Tatsächlich)

23. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

3. September 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

2. September 2026

Zuletzt verifiziert

1. September 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • BN104-102
  • 2025 (US NIH Stipendium/Vertrag: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
  • 2025-524689-74-00 (Ctis)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

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-Sharing-Zeitrahmen

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

IPD-Sharing-Zugriffskriterien

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.

Art der unterstützenden IPD-Freigabeinformationen

  • STUDIENPROTOKOLL
  • SAFT
  • ICF
  • CSR

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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