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- Klinische proef 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
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
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.
Studietype
Fase
- Fase 1
Contacten en locaties
Studie Locaties
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Missouri
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St Louis, Missouri, Verenigde Staten, 63110
- Washington University at St Louis
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
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.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Sequentiële toewijzing
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: 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
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Patients will receive BSB-2002 as a single IV infusion at day 1 following the lymphodepletion regime.
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Experimenteel: 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.
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Patients will receive BSB-2002 as a single IV infusion at day 1 following the lymphodepletion regime.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Number of participants with dose-limiting toxicity, adverse events (AEs) and serious AEs (SAEs)
Tijdsspanne: 365 days
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Incidence of dose-limiting toxicity, frequency and severity of adverse events (AEs) and serious AEs (SAEs)
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365 days
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Algehele overleving
Tijdsspanne: Gedurende 365 dagen
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Gedefinieerd als de tijd vanaf de behandeling tot het overlijden door welke oorzaak dan ook
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Gedurende 365 dagen
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Number of Patients with Relapse
Tijdsspanne: 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.
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365 days
|
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Cellular kinetics of BSB-2002 in peripheral blood
Tijdsspanne: 365 days
|
Quantitation of BSB-2002 (copies per μL of genomic DNA)
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365 days
|
Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Malignant Cell presence detected by Molecular MRD Methods
Tijdsspanne: 365 days
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Presence of malignant cells in the marrow, peripheral blood, or extramedullary sites detectable only by molecular methods
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365 days
|
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Cellular kinetics of serum cytokines and biomarkers
Tijdsspanne: 365 days
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Evaluation of inflammatory cytokines and other potential biomarkers
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365 days
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Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- BSB2002-CL-102
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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