Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT06819735

Study of DT-7012 as a Single Agent and in Combination With an Immune Checkpoint Inhibitor in Participants With Advanced Solid Tumors

Led by Domain Therapeutics Australia Pty Ltd · Updated on 2026-05-06

125

Participants Needed

9

Research Sites

131 weeks

Total Duration

On this page

Sponsors

D

Domain Therapeutics Australia Pty Ltd

Lead Sponsor

D

Domain Therapeutics SA

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Study of DT-7012 as a Single Agent and in Combination With an Immune Checkpoint Inhibitor in Participants With Advanced Solid Tumors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically or cytologically confirmed solid tumor, among selected cancer types, that is recurrent, locally advanced (not eligible for curative surgery or radiotherapy) or metastatic, has progressed after at least one line of systemic therapy and has no established curative option
  • Measurable disease per RECIST v1.1 as assessed by the local site investigator or radiologist
  • At least 1 tumor lesion accessible to biopsy per treating physician judgment
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Adequate organ function
Not Eligible

You will not qualify if you...

  • Any unresolved adverse events from previous anti-cancer therapies of grade 2 or higher, except alopecia
  • Prior severe immune-related adverse events leading to immunotherapy treatment discontinuation
  • Major surgery or significant traumatic injury within 4 weeks before Cycle 1 Day 1 without adequate recovery
  • Prior radiotherapy within 4 weeks before Cycle 1 Day 1 or limited field palliative radiotherapy within 2 weeks before Cycle 1 Day 1
  • Prior anti-CCR8 monoclonal antibody treatment received in an investigational trial

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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2
3
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Trial Site Locations

Total: 9 locations

1

Honor Health Research Institute

Scottsdale, Arizona, United States, 85258

Not Yet Recruiting

2

Macquarie University Clinical Trial Unit

North Ryde, New South Wales, Australia, 2109

Actively Recruiting

3

Cancer Research SA

Adelaide, South Australia, Australia, 5000

Actively Recruiting

4

Peninsula & South Eastern Haematology & Oncology Group

Frankston, Victoria, Australia, 3199

Actively Recruiting

5

Cabrini Health Limited

Malvern, Victoria, Australia, 3144

Actively Recruiting

6

One Clinical Research Pty Ltd

Nedlands, Western Australia, Australia, 6009

Actively Recruiting

7

Institut Bergonié

Bordeaux, France, 33076

Actively Recruiting

8

Hôpitaux Universitaires de Strasbourg

Strasbourg, France, 67200

Actively Recruiting

9

Institut Gustave Roussy

Villejuif, France, 94800

Actively Recruiting

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Research Team

C

Clinical Development

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

3

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