S243249 Monotherapy in Patients With Relapsed or Refractory Acute Leukemia With a KMT2A or NUP98 Translocation or Relapsed or Refractory AML With NPM1c Mutation
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
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Contact
Study Contact
- Name: Institut de Recherches Internationales Servier (I.R.I.S.)
- Phone Number: +33 1 55 72 60 00
- Email: scientificinformation@servier.com
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
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
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Incidence of Adverse Events (AEs)
Time Frame: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Severity of AEs
Time Frame: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of changes in laboratory values
Time Frame: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of changes in electrocardiogram (ECG)
Time Frame: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of changes in vital signs
Time Frame: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of AEs leading to dose interruption
Time Frame: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of AEs leading to dose modification
Time Frame: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of AEs leading to dose delays
Time Frame: Through Safety Follow-up (Approximately 3 years)
|
Through Safety Follow-up (Approximately 3 years)
|
|
Number of AEs leading to permanent treatment discontinuation
Time Frame: 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
Time Frame: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Overall response rate (ORR)
Time Frame: 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
Time Frame: Through Long-term Follow-up (Approximately 5 years)
|
CRc is CR + CRh + CRi
|
Through Long-term Follow-up (Approximately 5 years)
|
|
CR rate
Time Frame: 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
Time Frame: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Duration of response (DOR)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Cumulative relapse rate (CIR)
Time Frame: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Cumulative mortality (CID)
Time Frame: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Overall survival (OS)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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
Time Frame: 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
Time Frame: 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
Time Frame: Through Long-term Follow-up (Approximately 5 years)
|
Through Long-term Follow-up (Approximately 5 years)
|
|
|
Plasma concentration of S243249 and relevant metabolites
Time Frame: 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
Time Frame: 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
Time Frame: 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
Time Frame: 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)
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- BN104-102
- 2025 (U.S. NIH Grant/Contract: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
- 2025-524689-74-00 (Ctis)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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 Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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