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Dose Finding Study to Evaluate the Safety of BSB-2002 in Relapsed or Refractory Acute Myeloid Leukemia (AML) Patients With NPM1 Mutation

8. september 2026 oppdatert av: BlueSphere Bio, Inc

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

The goal of this clinical trial is to test BSB-2002 which is a new type of cellular therapy to treat blood cancer (AML). It will evaluate the safety of BSB-2002 and also determine whether it works to prevent relapse of your cancer.

Studieoversikt

Detaljert beskrivelse

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

Intervensjonell

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Missouri
      • St Louis, Missouri, Forente stater, 63110
        • Washington University at St Louis

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  1. Male or female patients, ages 18 years or older,
  2. AML diagnosed per ELN criteria1 which has been treated with at least two lines of therapy,

    1. which is relapsed (after previously complete remission, CR, CRh or CRi), or
    2. refractory (failed to achieve complete remission) to the last treatment*, *Primary refractory patients should have received at least two cycles of induction treatment
  3. Patients who are MRD positive by NGS for NPM1 after being MRD negative following the last treatment
  4. HLA-A*02:01,
  5. Positive for NPM1 mutation type A, D, G or H (see Appendix 3)2
  6. Adequate venous access for apheresis or agree to use of a central line for apheresis collection,
  7. Willing and able to provide informed consent and adhere to all study requirements.

Exclusion Criteria:

  1. Leukemic blast count of >20,000/μl. If the blast count can be maintained below the threshold with hydroxyurea, the patient would be eligible.
  2. Patients with extramedullary only AML.
  3. Patients that are candidates for hematopoietic stem cell transplant.
  4. Patients that are eligible to receive an approved targeted therapy.
  5. Treatment with other investigational agents within 5 half-lives of the planned dosing of BSB-2002 (day 1).
  6. Subject has had hematopoietic stem cell transplant (HSCT) and has any of the following:

    1. Is within 3 months of transplant;
    2. Has clinically significant graft-versus-host disease requiring systemic treatment;
    3. Has ≥ Grade 2 persistent non-hematological toxicity related to the transplant.
  7. Other malignancy that requires treatment.
  8. Uncontrolled bacterial, viral, or fungal infections at time of enrollment.
  9. Active Hepatitis B or C infection.
  10. Seropositive for Human Immunodeficiency Virus-1 or -2.
  11. CNS involvement refractory to intrathecal chemotherapy and/or standard cranial- spinal radiation.
  12. 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%.
  13. 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
  14. Total bilirubin > 2x upper limit of normal (unless attributed to Gilbert's Syndrome).
  15. AST or ALT > 3x upper limit of normal.
  16. Pregnant or lactating women.
  17. Eastern Cooperative Oncology Group (ECOG) performance status >2.
  18. Ongoing treatment with chronic immunosuppressants (e.g., cyclosporine or systemic steroids at any dose)
  19. 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.
  20. 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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Sekvensiell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of participants with dose-limiting toxicity, adverse events (AEs) and serious AEs (SAEs)
Tidsramme: 365 days
Incidence of dose-limiting toxicity, frequency and severity of adverse events (AEs) and serious AEs (SAEs)
365 days

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Total overlevelse
Tidsramme: Gjennom 365 dager
Definert som tiden fra behandling til død på grunn av en hvilken som helst årsak
Gjennom 365 dager
Number of Patients with Relapse
Tidsramme: 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
Tidsramme: 365 days
Quantitation of BSB-2002 (copies per μL of genomic DNA)
365 days

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Malignant Cell presence detected by Molecular MRD Methods
Tidsramme: 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
Tidsramme: 365 days
Evaluation of inflammatory cytokines and other potential biomarkers
365 days

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

21. april 2026

Primær fullføring (Faktiske)

8. september 2026

Studiet fullført (Faktiske)

8. september 2026

Datoer for studieregistrering

Først innsendt

21. april 2026

Først innsendt som oppfylte QC-kriteriene

27. april 2026

Først lagt ut (Faktiske)

5. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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