240
Participants
Start Date
August 3, 2021
Primary Completion Date
March 1, 2026
Study Completion Date
March 31, 2028
Ipilimumab
CTLA-4 (cytotoxic T-lymphocyte-associated protein 4) is a key regulator of T cell activity. Ipilimumab is a CTLA-4 immune checkpoint inhibitor that blocks T-cell inhibitory signals induced by the CTLA-4 pathway, increasing the number of tumor reactive T effector cells which mobilize to mount a direct T-cell immune attack against tumor cells. CTLA-4 blockade can also reduce T regulatory cell function, which may lead to an increase in anti-tumor immune response.
Nivolumab
A fully human immunoglobulin (Ig) G4 monoclonal antibody directed against the negative immunoregulatory human cell surface receptor programmed cell death-1 (PD-1,PCD-1) with immune checkpoint inhibitory and antineoplastic activities. Nivolumab binds to and blocks the activation of PD-1, an Ig superfamily transmembrane protein, by its ligands programmed cell death ligand 1 (PD-L1), overexpressed on certain cancer cells, and programmed cell death ligand 2 (PD-L2), which is primarily expressed on APCs (antigen presenting cells). This results in the activation of T-cells and cell-mediated immune responses against tumor cells or pathogens. Activated PD-1 negatively regulates T-cell activation and and plays a key role in in tumor evasion from host immunity.
Blacktown Hospital, Sydney
Calvary Mater Newcastle, Waratah
Border Medical Oncology Unit, Albury
Austin Health, Heidelberg
Goulburn Valley Health, Shepparton
Townsville Hospital and Health Service, Douglas
Townville Hospital and Health Service, Townsville
Cairns and Hinterland Hospital and Health Service, Cairns
Royal Hobart Hospital, Hobart
Orange Health Service, Orange
Royal Adelaide Hospital, Adelaide
Bendigo Health Services, Bendigo
Peninsula Health, Frankston
Barwon Health, Geelong
Peter MacCalllum Cancer Centre, Parkville
South West Healthcare, Warrnambool
Fiona Stanley Hospital, Perth
Auckland City Hospital, Auckland
Collaborators (1)
Bristol-Myers Squibb
INDUSTRY
Olivia Newton-John Cancer Research Institute
OTHER