OsteoAdapt SP
Clinical-stage regenerative biologic
An investigational bone graft therapeutic powered by AMP2, a proprietary rhBMP-2 variant engineered for targeted, sustained bone regeneration. It is being developed as an alternative to autologous and allograft bone in lumbar spinal fusion, and is in the pivotal OASIS trial after FDA approval in April 2026 to advance from feasibility to a pivotal study.
- Powered by AMP2, a proprietary rhBMP-2 variant
- Binds to the graft material so the dose stays localized and sustained
- Engineered to minimize off-target effects seen with conventional BMP-2
- Being studied across TLIF, ALIF and LLIF spinal fusion procedures simultaneously
- Targets symptomatic degenerative disease of the lumbosacral spine
- Prior clinical experience across roughly 100 participants at sites in Australia and Israel
Built for
Spine and orthopedic surgeons and the hospitals performing lumbar interbody fusion, reached through the regulatory and clinical trial pathway; ultimately patients with symptomatic degenerative lumbosacral spine disease and severe extremity or soft tissue injuries.