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Clinical evidence for predictable outcomes

Cavix was founded on our conviction that pets deserve nothing less than the best available care. Essential to achieving this is to assure that all Cavix products are grounded in established clinical evidence, starting with pre-clinical, safety and biocompatibility testing, and all the way through to clinical evaluation. Thorough documentation is therefore the foundation for any product we bring to market.

The first Cavix product, a synthetic bone graft based on our proprietary bone regenerative ceramic material, is currently in clinical documentation phase to ensure that pets, their owners and surgeons can rest assured that their treatment outcomes are predictable, with the highest possible level of care.

Current status of Cavix synthetic bone graft

Pre-clinical proof of concept

Porcine, spinal clinical model at Swedish University of Agricultural Sciences

  • CT follow-up at 3 month intervals

  • PET/CT and histology at termination

Clinical evaluation with companion animals at Vetsuisse Faculty University of Berne

  • Inclusion ongoing

  • CT follow-up at 3 month intervals

Clinical reference centers

  • Inclusion ongoing to establish a number of reference centers in Europe and the US to document broader user experiences and outcomes.

If you are interested in learning more about our technology, enrolling as a reference center, or exploring other partnership opportunities, see our Partnering Opportunities

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