If you are a biotech drug developer dealing with low patient response rates to Immune Checkpoint Inhibitors — this project developed NP137 that alleviates resistance to these treatments. This allows for the creation of combination therapies to increase overall survival.
Overcoming Cancer Immunotherapy Resistance Using a New Netrin-1 Targeting Antibody
Some cancer patients don't respond to the latest immune-boosting drugs because the tumor finds a way to hide or resist. This project uses a special antibody that acts like a key to unlock that resistance and stop the cancer from spreading. It essentially makes the tumor vulnerable again so the existing immunotherapy can actually work.
What needed solving
Many cancer patients do not respond to Immune Checkpoint Inhibitors (ICIs) due to primary or secondary resistance, leaving a significant care gap and limited treatment options.
What was built
A humanized monoclonal antibody (NP137) targeting netrin-1 and a corresponding proof-of-concept clinical trial to test its efficacy in combination with immunotherapy.
Who needs this
Who can put this to work
If you are an oncology clinic dealing with patients who are primary refractory to ICIs — this project developed a proof-of-concept clinical trial for NP137 that targets the epithelial-mesenchymal-transition. This provides a new treatment option for patients with limited choices.
If you are a CRO dealing with the need for first-in-class therapeutic antibodies — this project developed a humanized monoclonal antibody targeting netrin-1. It offers a validated mode-of-action published in Nature® for clinical trial execution.
Quick answers
What is the cost or pricing of the NP137 treatment?
Based on available project data, the specific cost or price of the treatment is not disclosed; however, the project received an EU contribution of EUR 2,500,000.
Is the technology ready for industrial scale production?
Based on available project data, the project is currently in the clinical trial phase to assess efficacy, which precedes full industrial scale-up.
What is the IP or licensing status of the antibody?
Based on available project data, the antibody NP137 was developed by NETRIS Pharma, and its mode-of-action has been published in two Nature® papers in August 2023.
What is the timeline for the clinical results?
The project period is from 2022-09-01 to 2025-09-30, suggesting results are expected by late 2025.
How is the antibody integrated with existing therapies?
NP137 is designed to be used on top of immunotherapy to alleviate resistance to Immune Checkpoint Inhibitors (ICIs).
Who built it
The project is led by a single partner, NETRIS PHARMA SAS, a French SME. This 100% industry-led consortium indicates a strong commercial drive, as the company is managing the entire transition from preclinical success to clinical trials without university partners in the consortium.
Contact NETRIS PHARMA SAS in Lyon, France
Talk to the team behind this work.
Contact us to explore licensing opportunities for NP137