7 Hills Pharma Begins Phase 1b/2a Trial of Alintegimod for aPD-1-resistant Tumors

6 September 2024

Sept. 3, 2024 – 7 Hills Pharma Inc. (“7 Hills” or “7HP”), a company dedicated to advancing cancer immunotherapies with innovative integrin activators, has announced that the first cancer patient in their clinical trial has been safely administered alintegimod. Alintegimod is an integrin-targeted agonist aimed at enhancing T cell activation and trafficking in patients who show resistance to immune checkpoint inhibitors.

The ongoing Phase 1b/2a multicenter study (NCT06362369) is funded by a $13.4 million grant from the Cancer Prevention and Research Institute of Texas (DP230062) and a $2.0 million grant from the National Cancer Institute (R44CA285207).

Alintegimod employs a novel mechanism of action, developed by the co-founders of 7 Hills Pharma, to enhance critical steps in the cancer immunity cycle, including immune cell trafficking, antigen presentation, and T cell activation.

“We are grateful to reach this significant milestone in alintegimod’s clinical development,” said Lionel D. Lewis, Chief Medical Officer of 7 Hills Pharma. “Administering alintegimod to our first cancer patient marks a crucial advancement in our mission to offer safer, more effective, and more accessible immunotherapy options to patients battling difficult-to-treat cancers.”

7 Hills Pharma specializes in developing small molecule immunotherapies for cancer treatment and stem cell therapy enhancement. Their compounds, which are first-in-concept allosteric integrin activators, utilize a unique mechanism to stabilize the cell-cell interactions necessary for an effective immune response and to accelerate the engraftment of transplanted hematopoietic stem cells.

Alintegimod, the lead integrin activator from 7 Hills Pharma, is an orally administered small molecule designed to safely enhance antigen-specific immune responses by selectively activating integrins LFA-1 and VLA-4. In preclinical models, alintegimod has demonstrated potential in improving the effectiveness of various immune checkpoint inhibitors. In a Phase I clinical trial, alintegimod showed good oral bioavailability and a clean safety profile at doses higher than therapeutic levels.

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