Back to search

BIA-Brukerstyrt innovasjonsarena

AXL as a therapeutic target in fibrosis; biology and biomarkers

Alternative title: Axl kinase som terapeutisk mål i fibrose; biologi og biomarkører

Awarded: NOK 10.7 mill.

Project Manager:

Project Number:

296534

Project Period:

2019 - 2023

Funding received from:

Location:

Subject Fields:

Partner countries:

Fibrotic disease, the accumulation of connective tissue and scar tissue in organs or tissues, is a leading cause of morbidity and mortality worldwide. There is a significant unmet medical need for new treatments that ameliorate fibrotic disease. BerGenBio ASA is developing drugs that inhibit the AXL pathway, a driver of not only drug resistant, immune evasive and metastatic cancer, but also an important mediator in fibrosis and infectious diseases such as COVID19. In the current project, BerGenBio will perform research and development to demonstrate that AXL-inhibition is a safe and effective treatment for fibrosis in human patients and to deepen our understanding of the mechanisms by which AXL-inhibition prevents and reduces fibrosis. To achieve these goals, BerGenBio is continuing to collaborate with academic groups that are experts in AXL signaling and on the role of AXL signaling in kidney and liver fibrosis. Pre-clinical data was presented as ePoster with speed-talk at ERA-EDTA in May and as poster at EASL in June.

The project has further validated AXL as a relevant and potential target in fibrotic diseases of kidney, liver and lung, and has contributed to several of the UN Sustainability development goals. Good health and wellbeing: Through completion of a clinical Ph1a and Ph1b study, we have confirmed safety and tolerability of our proprietary anti-AXL antibody tilvestamab and determined PK and target engagement in a selected patient population. Quality education: Funding from this project has been important in the training of several PhD students both internationally in BerGenBio and at collaborating academic institutions. Industry, Innovation and Infrastructure: This project has contributed to further knowledge of the important role of AXL in fibrotic pathology in experimental models. Several model systems and assays have been developed to allow studies of inhibition of AXL using the tilvestamab monoclonal antibody and comparative studies between the small molecule AXL inhibitor bemcentinib and tilvestamab.

BerGenBio ASA is a clinical-stage oncology company advancing first-in-class, selective AXL kinase inhibitors against aggressive diseases. The receptor tyrosine kinase AXL is becoming a profiled target for developing drugs to treat resistant and metastatic cancer. Over the last decade it has become evident that the AXL pathway also plays a decisive role in fibrosis. Fibrotic diseases of the lung, liver and kidney are a significant cause of death worldwide. BerGenBio’s selective AXL inhibitors are effective in preventing fibrosis in a variety of model systems. The objective of this project is to perform research and development to demonstrate that AXL-inhibition is a safe and effective treatment for fibrosis in human patients and to deepen our understanding of the mechanisms by which AXL-inhibition prevents and reduces fibrosis. To achieve these goals, BerGenBio has established collaborations with academic groups that are experts in AXL signaling (Prof. James B Lorens, Department of Biomedicine, UoB, Bergen, Norway) and on the role of AXL signaling in liver fibrosis (PhD Albert Morales, Institute of Biomedical Research, Barcelona, Spain).

Funding scheme:

BIA-Brukerstyrt innovasjonsarena