Kuros statement on media inquiry concerning former Board member
Ad-hoc announcement pursuant to Article 53 of the SIX listing rules
Kuros statement on media inquiry concerning former Board member
Schlieren (
For further information, please contact:
| Investor Relations | Chief Financial Officer |
| Tel +41 43 268 32 31 | Tel +41 44 733 47 41 |
| IR@kurosbio.com | daniel.geiger@kurosbio.com |
About MagnetOs
Growing bone with MagnetOsTM gives surgeons confidence where it matters most – delivering predictable fusion outcomes.1 In a Level I human clinical study published in Spine, MagnetOs achieved nearly twice the fusion rate (79% vs. 47%) of autograft in posterolateral fusions (PLFs).1 Among active smokers – who made up 1 in 5 patients – the fusion difference between MagnetOs and autograft was even more dramatic.*†1,2 MagnetOs grows bone on its own thanks to NeedleGripTM – a proprietary submicron surface technology that harnesses the immune system to stimulate bone growth, without added cells or growth factors.‡§3-8 Ready-to-use, easy to mold, and reliably staying put9, MagnetOs carries no intrinsic risk of human tissue-related disease transmission and is FDA cleared for use throughout the spine, including interbody procedures. ¶5-8
Indications Statement
Please refer to the instructions for use for your local region for a full list of indications, contraindications, warnings, and precautions.
About
Forward Looking Statements
This media release contains certain forward-looking statements that involve risks and uncertainties that could cause actual results to be materially different from historical results or from any future results expressed or implied by such forward-looking statements. You are urged to consider statements that include the words “will” or “expect” or the negative of those words or other similar words to be uncertain and forward-looking. Factors that may cause actual results to differ materially from any future results expressed or implied by any forward-looking statements include scientific, business, economic and financial factors. Against the background of these uncertainties, readers should not rely on forward-looking statements. The Company assumes no responsibility for updating forward-looking statements or adapting them to future events or developments.
* 19 of initial 100 patients were active smokers.
† Radiographic fusion data of the smoker subgroup were not statistically analyzed as a subgroup and were not included in the peer-reviewed publication of the study.2
‡ Results from in vitro or in vivo laboratory testing may not be predictive of clinical experience in humans. For important safety and intended use information please visit kurosbio.com.
§ MagnetOs is not cleared by the FDA or TGA as an osteoinductive bone graft.
¶ MagnetOs must also be used with an intervertebral body fusion device cleared by FDA for use with a bone void filler. MagnetOs Flex Matrix must be hydrated with BMA & mixed with autograft in posterolateral spine & intervertebral disc space. MagnetOs Granules must be hydrated with blood in the intervertebral disc space.
- Stempels, et al. Spine. 2024;49(19):1323-1331.
- van Dijk, LA. 24th SGS Annual Meeting (
Swiss Society of Spinal Surgery ).Basel, Switzerland .Aug 2024 . van Dijk , et al. eCM. 2021;41:756-73.van Dijk , et al. J Immunol Regen Med. 2023;19:100070.- Instructions for Use (IFU) MagnetOs Granules.
- Instructions for Use (IFU) MagnetOs Putty.
- Instructions for Use (IFU) MagnetOs Easypack Putty.
- Instructions for Use (IFU) MagnetOs Flex Matrix.
- Data on file. MagnetOs Putty and MagnetOs Easypack Putty.
Attachment

Source: Kuros Biosciences AG