
FMC BioPolymer (Norway)
Wikidata: Q30256486
FMC BioPolymer (Norway)
3 Projects, page 1 of 1
assignment_turned_in Project2012 - 2015Partners:Rescoll (France), FMC, PIW IMPULS, SIGEA, FMC BioPolymer (Norway) +2 partnersRescoll (France),FMC,PIW IMPULS,SIGEA,FMC BioPolymer (Norway),UM,UNITSFunder: European Commission Project Code: 280929more_vert assignment_turned_in Project2009 - 2014Partners:Vilnius University, Jobst Technologies (Germany), VIROLOGICKY USTAV SLOVENSKEJ AKADEMIE VIED, University of Manchester, ViVoX +17 partnersVilnius University,Jobst Technologies (Germany),VIROLOGICKY USTAV SLOVENSKEJ AKADEMIE VIED,University of Manchester,ViVoX,CNRS,FMC BioPolymer (Norway),University of Florence,KI,UOXF,UCL,University of Edinburgh,AUH,MAASTRO,FMC,Oslo University Hospital,STICHTING RADBOUD UNIVERSITEIT,UiO,DHM,University of Freiburg,UM,UAMFunder: European Commission Project Code: 222741more_vert Open Access Mandate for Publications assignment_turned_in Project2015 - 2019Partners:FMC, WFUHS, UCL, EFS, NIT +6 partnersFMC,WFUHS,UCL,EFS,NIT,Charité - University Medicine Berlin,CEA,FMC BioPolymer (Norway),UGA,UJF,ERSFunder: European Commission Project Code: 646272Overall Budget: 7,998,880 EURFunder Contribution: 7,998,880 EURThe key therapeutic issue in diabetes mellitus type I and II is glycaemic control. Reductions of constant self-control, of insulin injections, and of long-term complications would have tremendous benefit for quality of life. The best therapy option is the transplantation of allogeneic islet cells, but the current state of the art limits the applicability of this approach. Implanting unprotected grafts requires lifelong administration of immunosuppressants, and protecting the cells against adverse immune reactions by current encapsulation strategies reduces their functionality and survival to an extend that makes frequent ‘refresher’ implantations necessary. Currently, a maximum of 2 years glycaemia regulation has been shown for the encapsulated approach. In BIOCAPAN, bringing experts from different fields all together, we aim at developing an innovative treatment, based on the implantation of allogeneic islet cells that are embedded in a complex microcapsule. We will design a GMP-grade bioactive microcapsule that will maximize the long-term functionality and survival of pancreatic islets by prevention of pericapsular fibrotic overgrowth, in situ oxygenation, innovative extracellular matrix microenvironment reconstruction and immune-system modulation. We will establish a GMP-grade microfluidic microencapsulation platform to protect freshly harvested islets quickly in a standardized and reproducible way. We aim for full preclinical validation and we will establish a complete protocol in accordance with the provisions of the Advanced Therapy Medicinal Products Regulation, in order to start clinical trials within one year after the end of the project. We aim for 5-years insulin injection free treatment, without immunosuppressants, which would tremendously benefit diabetes mellitus patients who require insulin (all Type I and about one in six Type II Diabetes Mellitus patients).
more_vert