BONESUPPORT AB (STO:BONEX), an orthobiologics company focused on the management of bone voids, announced on Friday the publication of ground-breaking data on bone remodelling of CERAMENT in pre-clinical model.
This study, entitled 'Establishment and effects of allograft and synthetic bone graft substitute treatment of a critical size metaphyseal bone defect model in the sheep femur' is published in APMIS (Acta Pathologica, Microbiologica et Immunologica Scandinavica) Journal of Pathology, Microbiology and Immunology.
Dr Michael Diefenbeck, the company's EVP R&D, Medical & Clinical Affairs, is the senior author of the publication
Reportedly, this pilot study represents an important initial step towards establishing a clinically relevant large animal model that allows thorough investigation of bone graft substitute-mediated bone defect regeneration, in-depth analysis of its interaction with host bone and accurate documentation of the resulting bone remodelling over time.
Also, the combination of different imaging methods like radiographs, μCT, MRI and histology provides a clearer insight into the healing process of the bone tissue. Histological evaluations helped to confirm the resorption of CERAMENT and regeneration of trabecular bone in the periphery of the void as early as three months.
According to the company, this research was performed in collaboration with authors from the Universities in Copenhagen, Munich and Jena, namely Dr Werner Hettwer, Dr Peter Horstmann, Dr Sabine Bischoff, Dr Daniel Güllmar, Prof Jürgen Reichenbach, Dr Patrina Su Ping Poh, Prof Martijn van Griensven and Dr Florian Gras.
Bone support Holding develops and commercialises innovative injectable bio-ceramic bone graft substitutes that remodel to the patient's own bone and have the capability of eluting drugs. The company's bone graft substitutes are based on the patented technology platform CERAMENT.
NeuroSense Therapeutics completes safety evaluation of PrimeC in Alzheimer's Phase 2 study
BrioHealth Solutions enrols 100th participant in BrioVAD System trial
Faron launches BLAZE trial with Institute of Cancer Research to address immunotherapy resistance
AstraZeneca secures US Breakthrough status for Enhertu in early breast cancer
Ipsen licenses Simcere Zaiming antibody-drug conjugate for global development
Shield Therapeutics wins FDA approval to expand ACCRUFeR use to adolescents
Hansa Biopharma submits imlifidase Biologics License Application to FDA
T-MAXIMUM Pharmaceutical receives IND approval to start Phase II trial of MT027 for rGBM
Ipsen closes Phase II FALKON trial after missing primary endpoint in FOP
Curasight reports first patient dosed in Phase 1 uTREAT trial in brain cancer
Clywedog Therapeutics activates all clinical centres and patient dosing in balomenib Phase 1b study
PRISM BioLab partners with Talus Bioscience to address TF and PPI targets
Thryv Therapeutics reports positive Phase 1 results for THRV-1268