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A Two-Part Open Label Phase 1 Multicentre Study Evaluating the Safety of INT2104 Infusions in Female and Male Participants Aged 18 Years of Age and Older With Refractory/Relapsing B-cell Malignancies

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Trial Profile

A Two-Part Open Label Phase 1 Multicentre Study Evaluating the Safety of INT2104 Infusions in Female and Male Participants Aged 18 Years of Age and Older With Refractory/Relapsing B-cell Malignancies

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 10 Jan 2025

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At a glance

  • Drugs INT 2104 (Primary)
  • Indications B-cell lymphoma; Burkitt's lymphoma; Non-Hodgkin's lymphoma; Precursor cell lymphoblastic leukaemia-lymphoma
  • Focus Adverse reactions; First in man; Proof of concept
  • Acronyms INVISE
  • Sponsors Interius BioTherapeutics

    • Most Recent Events

    • 07 Jan 2025 According to an Interius BioTherapeutics media release, the interim safety and proof-of-concept data to be presented at a scientific meeting in 2H 2025
    • 07 Jan 2025 According to an Interius BioTherapeutics media release, the German regulatory agency, the Paul Ehrlich Institute, granted approval to expand the INVISE Phase 1 clinical trial evaluating INT2104 for the treatment of B-cell malignancies to Europe
    • 23 Oct 2024 According to an Interius BioTherapeutics media release, company looks forward to sharing interim clinical safety and proof-of-concept data at a scientific meeting next year (1H 2025).

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