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Study of DT-7012 as a Single Agent and in Combination With an Immune Checkpoint Inhibitor in Participants With Advanced Solid Tumors
Sponsor: Domain Therapeutics Australia Pty Ltd
Summary
This is a phase 1/2, dose-escalation, clinical study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of DT-7012 (an anti-CCR8 monoclonal antibody) as a single agent and in combination with an immune checkpoint inhibitor in adult participants with selected advanced solid tumors.
Official title: A Phase 1/2, Multicentre, Open-label Clinical Trial of DT-7012 as Monotherapy and in Combination With an Immune Checkpoint Inhibitor in Participants With Selected Advanced Solid Tumors (DOMISOL, DOmain_therapeutics Monoclonal antIbody for SOLid Tumors)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
125
Start Date
2025-06-25
Completion Date
2028-01
Last Updated
2026-03-10
Healthy Volunteers
No
Conditions
Interventions
DT-7012
Intravenous infusion
Immune checkpoint inhibitor
Intravenous infusion
Locations (8)
Macquarie University Clinical Trial Unit
North Ryde, New South Wales, Australia
Cancer Research SA
Adelaide, South Australia, Australia
Peninsula & South Eastern Haematology & Oncology Group
Frankston, Victoria, Australia
Cabrini Health Limited
Malvern, Victoria, Australia
One Clinical Research Pty Ltd
Nedlands, Western Australia, Australia
Institut Bergonié
Bordeaux, France
Hôpitaux Universitaires de Strasbourg
Strasbourg, France
Institut Gustave Roussy
Villejuif, France