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A Phase 1 multicenter study evaluating the feasibility, safety, and efficacy of lonitoclax in patients with relapsed/refractory chronic lymphocytic leukemia, small lymphocytic lymphoma, and select low-grade lymphomas.

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A Phase 1 multicenter study evaluating the feasibility, safety, and efficacy of lonitoclax in patients with relapsed/refractory chronic lymphocytic leukemia, small lymphocytic lymphoma, and select low-grade lymphomas.

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 17 Oct 2024

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At a glance

  • Drugs Lonitoclax (Primary)
  • Indications Chronic lymphocytic leukaemia; Lymphoma
  • Focus Adverse reactions

    • Most Recent Events

    • 17 Oct 2024 New trial record
    • 16 Oct 2024 According to Expert Systems media release, Expert Systems proudly announces a major milestone in its partnership with Lomond Therapeutics, FDA clearance for Lomonds IND represents a key milestone in collaboration
    • 15 Oct 2024 According to Lomond Therapeutics Media Release, announced that the U.S. Food and Drug Administration (FDA) has cleared Lomond's Investigational New Drug (IND) application for a Phase 1 multicenter study evaluating the feasibility, safety, and efficacy of lonitoclax in patients with relapsed/refractory chronic lymphocytic leukemia, small lymphocytic lymphoma, and select low-grade lymphomas.

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