AU-007 is designed utilising AI for leveraging interleukin-2 to eliminate solid tumours. Credit: Peddalanka Ramesh Babu / Shutterstock.com.

Aulos Bioscience has unveiled plans to begin the Phase II portion of its Phase I/II clinical study of human IgG1 monoclonal antibody, AU-007, to treat patients with unresectable locally advanced or metastatic solid tumour cancers of the kidney and skin.

AU-007 is designed utilising artificial intelligence (AI) for leveraging interleukin-2 (IL-2) to eliminate solid tumours.

Created by Biolojic Design, it is claimed to be the first computationally designed monoclonal antibody to be assessed in a clinical study.

It is expected to hold the potential to attach accurately to the IL-2 portion that binds to CD25, which prevents binding of IL-2 to IL-2 receptors on regulatory T cells (Tregs), pulmonary tissue vasculature, and eosinophils.

The first Phase II expansion cohorts will concentrate on renal cell carcinoma (RCC) and melanoma.

They will assess the antibody along with a single loading dose of low-dose, subcutaneous Proleukin (aldesleukin; recombinant human IL-2), or with AU-007 and Proleukin given every two weeks.

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Aulos Bioscience CEO Aron Knickerbocker said: “Since our last data cutoff date of October 13, 2023 (data presented at SITC), new data indicate clinical activity in several patients, including disease control and objective response results.

“This is encouraging as the anti-tumour activity has been observed in heavily pre-treated patients whose tumours had progressed through checkpoint inhibitors. We look forward to the Phase II portion of this study and presenting clinical data from the expansion cohorts next year.”

The Phase I dose escalation cohort findings show that AU-007 is well tolerated when used alone or in combination with Proleukin.

No reports of pulmonary or generalised edema, vasculature leakage, or dose-limiting toxicity have been observed so far.