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Lenzilumab - Humanigen

Drug Profile

Lenzilumab - Humanigen

Alternative Names: Humaneered® anti-human GM-CSF monoclonal Antibody; KB-003

Latest Information Update: 06 Oct 2020

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At a glance

  • Originator KaloBios Pharmaceuticals
  • Developer Humanigen; KaloBios Pharmaceuticals; Kite Pharma
  • Class Anti-inflammatories; Antiallergics; Antiasthmatics; Antineoplastics; Antirheumatics; Antivirals; Immunotherapies; Monoclonal antibodies
  • Mechanism of Action Granulocyte macrophage colony stimulating factor antagonists
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes
  • Available For Licensing Yes - Asthma; COVID 2019 infections

Highest Development Phases

  • Phase III Pneumonia
  • Phase I/II B-cell lymphoma; Drug hypersensitivity
  • Phase I Chronic myelomonocytic leukaemia
  • Preclinical Graft-versus-host disease; Precursor cell lymphoblastic leukaemia-lymphoma
  • Research Solid tumours
  • Discontinued Asthma; Rheumatoid arthritis

Most Recent Events

  • 12 Oct 2020 National Institute of Allergy and Infectious Diseases plans a phase II ACTIV-5/BET trial for COVID-2019 infections (Combination therapy) in USA (IV, Infusion) in October 2020 (NCT04583969)
  • 05 Oct 2020 Phase-III clinical trials in Pneumonia (Combination therapy) in Brazil (IV)
  • 05 Oct 2020 Humanigen intends to submit Biologics License Application to US FDA for the treatment of Pneumonia associated with COVID-19 infections
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