Anti-IL-6 | A breakthrough active immunotherapy for the treatment of osteoarthritis

Summary
Osteoarthritis is a debilitating disease affecting the joint and a leading cause of disability worldwide. It affects at least 250m people and incurs healthcare costs of toward 0.5% of the GDP.
Peptinov is developing an active immunotherapy that can halt inflammation-driven destruction of the cartilage in the joints. We use a unique approach to neutralise a key pro-inflammatory protein (IL-6) driving chronic inflammation. Our vaccine-like approach stimulates the patient’s own immune system to produce antibodies against excess IL-6 and neutralise its biological function. By doing so we will halt disease progression.
Our treatment will cost 5-10% of conventional immunotherapies as we inject patients with inexpensive, immunogenic peptides to stimulate production of endogenous antibodies. Phase I clinical trial yielded very encouraging preliminary safety and tolerability data on 24 patients. This project will implement the Phase II clinical trial and make our therapy out-licensing ready.
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Web resources: https://cordis.europa.eu/project/id/101145362
Start date: 01-03-2024
End date: 28-02-2026
Total budget - Public funding: 3 965 000,00 Euro - 2 499 999,00 Euro
Cordis data

Original description

Osteoarthritis is a debilitating disease affecting the joint and a leading cause of disability worldwide. It affects at least 250m people and incurs healthcare costs of toward 0.5% of the GDP.
Peptinov is developing an active immunotherapy that can halt inflammation-driven destruction of the cartilage in the joints. We use a unique approach to neutralise a key pro-inflammatory protein (IL-6) driving chronic inflammation. Our vaccine-like approach stimulates the patient’s own immune system to produce antibodies against excess IL-6 and neutralise its biological function. By doing so we will halt disease progression.
Our treatment will cost 5-10% of conventional immunotherapies as we inject patients with inexpensive, immunogenic peptides to stimulate production of endogenous antibodies. Phase I clinical trial yielded very encouraging preliminary safety and tolerability data on 24 patients. This project will implement the Phase II clinical trial and make our therapy out-licensing ready.

Status

SIGNED

Call topic

HORIZON-EIC-2023-ACCELERATOROPEN-01

Update Date

12-03-2024
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