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

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

I'm a Healthcare Professional

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

Cancer patient talking to doctor

I'm a Patient

The imneskibart solid tumor study is for people 18 years and older with advanced or metastatic cancer.

Cancer survivor women on the beach

About the Clinical Trial

The imneskibart solid tumor 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 enrolling patients at multiple sites in the United States.

 

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 must be 18 years of age and older with refractory or resistant advanced solid tumor cancer who are interested in participating in a clinical trial to evaluate an investigational IL-2 therapeutic.

Where is the study?

The study is enrolling patients at multiple cancer care centers in the U.S. 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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