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RECRUITING
NCT06819735
PHASE1/PHASE2

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

View on ClinicalTrials.gov

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

Interventions

DRUG

DT-7012

Intravenous infusion

DRUG

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