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A Phase 1/2 Open-label Study to Investigate the Safety, Efficacy, and Pharmacokinetics of Administration of Subcutaneous Blinatumomab for the Treatment of Adults and Adolescents With Relapsed or Refractory B Cell Precursor Acute Lymphoblastic Leukemia (R/R B-ALL) and Minimal Residual Disease Positive (MRD+) B-ALL

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Trial Profile

A Phase 1/2 Open-label Study to Investigate the Safety, Efficacy, and Pharmacokinetics of Administration of Subcutaneous Blinatumomab for the Treatment of Adults and Adolescents With Relapsed or Refractory B Cell Precursor Acute Lymphoblastic Leukemia (R/R B-ALL) and Minimal Residual Disease Positive (MRD+) B-ALL

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 09 Mar 2026

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At a glance

  • Drugs Blinatumomab (Primary)
  • Indications Precursor B-cell lymphoblastic leukaemia-lymphoma
  • Focus Adverse reactions; Pharmacokinetics; Therapeutic Use
  • Sponsors Amgen

Most Recent Events

  • 17 Dec 2025 Planned primary completion date changed from 27 Jul 2027 to 24 Nov 2027.
  • 03 Nov 2025 Planned primary completion date changed from 24 Dec 2027 to 27 Jul 2027.
  • 27 Aug 2025 Status changed from active, no longer recruiting to recruiting.

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