- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07566585
Dose Finding Study to Evaluate the Safety of BSB-2002 in Relapsed or Refractory Acute Myeloid Leukemia (AML) Patients With NPM1 Mutation
A Phase 1 Multicenter Dose Finding Study to Evaluate the Safety of BSB-2002 in Relapsed or Refractory Acute Myeloid Leukemia (AML) Patients With NPM1 Mutation
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
This is a Phase I, multicenter, open-label, non-randomized study to characterize the safety and clinical activity of BSB-2002, a genetically modified autologous T cell product incorporating an HLA-A*02:01-restricted mutant NPM1-directed T cell receptor (TCR), administered to patients with relapsed or refractory acute myeloid leukemia (AML). Enrolled patients must be HLA-A*02:01+ and positive for the NPM1 mutation which produces the alternative amino acid sequence CLAVEEVSL (Type A, D, G or H).
The study is an adaptive dose escalation design with up to 3 cohorts to evaluate single doses of BSB-2002, employing the 3+3 design.
Tipo de estudio
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Missouri
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St Louis, Missouri, Estados Unidos, 63110
- Washington University at St Louis
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Male or female patients, ages 18 years or older,
AML diagnosed per ELN criteria1 which has been treated with at least two lines of therapy,
- which is relapsed (after previously complete remission, CR, CRh or CRi), or
- refractory (failed to achieve complete remission) to the last treatment*, *Primary refractory patients should have received at least two cycles of induction treatment
- Patients who are MRD positive by NGS for NPM1 after being MRD negative following the last treatment
- HLA-A*02:01,
- Positive for NPM1 mutation type A, D, G or H (see Appendix 3)2
- Adequate venous access for apheresis or agree to use of a central line for apheresis collection,
- Willing and able to provide informed consent and adhere to all study requirements.
Exclusion Criteria:
- Leukemic blast count of >20,000/μl. If the blast count can be maintained below the threshold with hydroxyurea, the patient would be eligible.
- Patients with extramedullary only AML.
- Patients that are candidates for hematopoietic stem cell transplant.
- Patients that are eligible to receive an approved targeted therapy.
- Treatment with other investigational agents within 5 half-lives of the planned dosing of BSB-2002 (day 1).
Subject has had hematopoietic stem cell transplant (HSCT) and has any of the following:
- Is within 3 months of transplant;
- Has clinically significant graft-versus-host disease requiring systemic treatment;
- Has ≥ Grade 2 persistent non-hematological toxicity related to the transplant.
- Other malignancy that requires treatment.
- Uncontrolled bacterial, viral, or fungal infections at time of enrollment.
- Active Hepatitis B or C infection.
- Seropositive for Human Immunodeficiency Virus-1 or -2.
- CNS involvement refractory to intrathecal chemotherapy and/or standard cranial- spinal radiation.
- Subject has congestive heart failure NYHA class 3 or 4, or subject with a history of congestive heart failure NYHA class 3 or 4 in the past, unless an echocardiogram performed within 3 months prior to study entry results in a left ventricular ejection fraction that is ≥ 45%.
- Renal insufficiency, with estimated creatinine clearance of < 40 ml/min/1.73m2 by the Cockcroft-Gault equation with adjustment if the weight is ≥ 125% of ideal body weight OR inadequate renal function defined by serum creatinine > 1.6 mg/dL
- Total bilirubin > 2x upper limit of normal (unless attributed to Gilbert's Syndrome).
- AST or ALT > 3x upper limit of normal.
- Pregnant or lactating women.
- Eastern Cooperative Oncology Group (ECOG) performance status >2.
- Ongoing treatment with chronic immunosuppressants (e.g., cyclosporine or systemic steroids at any dose)
- Women of childbearing potential (WOCBP) and men who are fertile and are unwilling to use an effective birth control method or abstinence for 12 months. Effective forms of birth control are listed in the Contraception section.
- Any condition, in the judgement of the Investigator, that would interfere with study participation, pose a significant risk to the patient, or interfere with study data interpretation.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Dose Escalation Cohorts
AML HLA-A*02:01 and Positive for NPM1 mutation type A, D, G or H patients with an identified will be dosed in dose escalation cohorts
|
Patients will receive BSB-2002 as a single IV infusion at day 1 following the lymphodepletion regime.
|
|
Experimental: Expansion Cohort
Once the maximum tolerated dose (MTD) or promising dose is reached additional AML HLA-A*02:01 and Positive for NPM1 mutation type A, D, G or H patients will be enrolled in the expansion cohort.
|
Patients will receive BSB-2002 as a single IV infusion at day 1 following the lymphodepletion regime.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of participants with dose-limiting toxicity, adverse events (AEs) and serious AEs (SAEs)
Periodo de tiempo: 365 days
|
Incidence of dose-limiting toxicity, frequency and severity of adverse events (AEs) and serious AEs (SAEs)
|
365 days
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Supervivencia general
Periodo de tiempo: Durante 365 días
|
Definido como el tiempo desde el tratamiento hasta la muerte por cualquier causa.
|
Durante 365 días
|
|
Number of Patients with Relapse
Periodo de tiempo: 365 days
|
Presence of malignant cells in marrow (>5%), peripheral blood (>1%), or extramedullary sites by histopathology after achievement of CR, CRh or CRi any time after study treatment.
|
365 days
|
|
Cellular kinetics of BSB-2002 in peripheral blood
Periodo de tiempo: 365 days
|
Quantitation of BSB-2002 (copies per μL of genomic DNA)
|
365 days
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Malignant Cell presence detected by Molecular MRD Methods
Periodo de tiempo: 365 days
|
Presence of malignant cells in the marrow, peripheral blood, or extramedullary sites detectable only by molecular methods
|
365 days
|
|
Cellular kinetics of serum cytokines and biomarkers
Periodo de tiempo: 365 days
|
Evaluation of inflammatory cytokines and other potential biomarkers
|
365 days
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- BSB2002-CL-102
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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