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Imneskibart (AU-007) Immunotherapy for Advanced or Metastatic Cancer

A clinical trial for patients with melanoma, lung and other cancers

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I'm a Patient

The imneskibart solid tumour study is for males or females 18 years and older with advanced or metastatic cancer.

Doctor and Patient

I'm a Health Professional

A Phase 1/2 study investigating a novel human monoclonal antibody in patients with advanced or metastatic cancer.

About the Clinical Trial

The imneskibart solid tumour study is an open label Phase 1/2 study evaluating the safety, tolerability and immunogenicity of imneskibart in patients with unresectable locally advanced or metastatic cancer. It is currently enrolling patients in New South Wales, Victoria and South Australia.

 

Cancer eligibility includes cutaneous melanoma and non-small cell lung cancer. Patients who have failed or progressed on anti-PD-1 or anti-PD-L1 therapy may be enrolled in the study.

Study Details

Who can qualify?

Eligible participants can be males or females 18 years of age and older with refractory or resistant advanced solid tumour cancer who are interested in participating in a clinical trial to evaluate an investigational IL-2 therapeutic.

Where is the study?

The study is taking place at multiple cancer care centres in Australia. It is being led by seasoned oncologists with expertise in treating advanced cancers and conducting early phase cancer studies.

How does it work?

The Phase 1/2 trial is an open label study evaluating the safety, tolerability, immunogenicity and clinical activity of imneskibart, a human IgG1 monoclonal antibody designed by leveraging artificial intelligence.

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