- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07722312
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 de septiembre de 2026 actualizado por: 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.
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
80
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: Institut de Recherches Internationales Servier (I.R.I.S.)
- Número de teléfono: +33 1 55 72 60 00
- Correo electrónico: scientificinformation@servier.com
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
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.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
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
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Incidence of Adverse Events (AEs)
Periodo de tiempo: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Severity of AEs
Periodo de tiempo: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of changes in laboratory values
Periodo de tiempo: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of changes in electrocardiogram (ECG)
Periodo de tiempo: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of changes in vital signs
Periodo de tiempo: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of AEs leading to dose interruption
Periodo de tiempo: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of AEs leading to dose modification
Periodo de tiempo: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of AEs leading to dose delays
Periodo de tiempo: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of AEs leading to permanent treatment discontinuation
Periodo de tiempo: 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
Periodo de tiempo: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Overall response rate (ORR)
Periodo de tiempo: 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
Periodo de tiempo: Through Long-term Follow-up (Approximately 5 years)
|
CRc is CR + CRh + CRi
|
Through Long-term Follow-up (Approximately 5 years)
|
|
CR rate
Periodo de tiempo: 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
Periodo de tiempo: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Duration of response (DOR)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Cumulative relapse rate (CIR)
Periodo de tiempo: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Cumulative mortality (CID)
Periodo de tiempo: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Overall survival (OS)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Plasma concentration of S243249 and relevant metabolites
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
20 de octubre de 2026
Finalización primaria (Estimado)
11 de agosto de 2029
Finalización del estudio (Estimado)
25 de agosto de 2030
Fechas de registro del estudio
Enviado por primera vez
13 de julio de 2026
Primero enviado que cumplió con los criterios de control de calidad
22 de julio de 2026
Publicado por primera vez (Actual)
23 de julio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
3 de septiembre de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
2 de septiembre de 2026
Última verificación
1 de septiembre de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- BN104-102
- 2025 (Subvención/contrato del NIH de EE. UU.: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
- 2025-524689-74-00 (Ctis)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
SÍ
Descripción del plan IPD
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.
Marco de tiempo para compartir IPD
After Marketing Authorization in EEA or US if the study is used for the approval.
Criterios de acceso compartido de IPD
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.
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
- CIF
- RSC
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Sí
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .