# Effect of vosoritide on spine morphology in children with achondroplasia: 1-year results from a randomized phase 2 study

**Authors:** Melita Irving, Ravi Savarirayan, Julie E Hoover-Fong, Anne Dee, Swati Mukherjee, Christine Rivat, Ian Sabir, Klane K White

PMC · DOI: 10.1210/jendso/bvag008 · Journal of the Endocrine Society · 2026-02-20

## TL;DR

A 1-year study found that vosoritide, a treatment for achondroplasia, improved spinal structure in young children, potentially reducing the risk of spinal stenosis.

## Contribution

This is the first study to assess vosoritide's impact on spinal morphology in children with achondroplasia.

## Key findings

- Vosoritide improved interpedicular distance and spinal canal width compared to placebo after one year.
- Treatment reduced the natural increase in thoracolumbar kyphosis angle in younger children.
- Fewer children on vosoritide had pathological kyphosis angles compared to those on placebo.

## Abstract

Achondroplasia is a skeletal dysplasia condition caused by reduced endochondral ossification resulting in disproportionate short stature and skeletal deformities, including thoracolumbar kyphosis (TLK) and spinal stenosis. Vosoritide, the first and only approved targeted therapy for achondroplasia, increases bone growth, but its impact on spinal morphology has not been assessed. The randomized, double-blind, placebo-controlled phase 2 CANOPY ACH-2I study (111-206; NCT03583697) evaluated the safety and efficacy of vosoritide in 75 children aged 0 to <5 years. Interpedicular distance (IPD), sagittal width of the lumbar spinal canal, and TLK angle were measured on spinal radiographs taken at baseline and 1 year after vosoritide or placebo treatment. Differences in least-squares mean (LSM) change from baseline (95% CI) between treatment groups were determined with an analysis of covariance model. Measurable improvements in IPD and spinal canal width across L1 to L5 were observed with vosoritide compared with placebo after 1 year. L4 was the most impacted by vosoritide for IPD (LSM difference [95% CI], 0.509 [−0.034 to 1.052] mm, P = .066) and canal width (1.433 [0.547 to 2.320] mm, P = .002). Vosoritide treatment also reduced the natural increase in TLK angle in children 0 to <0.5 years and provided greater improvements in children ≥0.5 to <5 years. After 1 year, fewer children treated with vosoritide (33.3%) vs placebo (59.3%) had pathological (≥20°) TLK angles (P = .037). These preliminary results suggest that early vosoritide treatment may improve spinal morphology and reduce the risk of spinal stenosis in children with achondroplasia.

Clinical Trial Information: NCT03583697.

## Linked entities

- **Chemicals:** vosoritide (PubChem CID 119058036)
- **Diseases:** achondroplasia (MONDO:0007037), spinal stenosis (MONDO:0005965)

## Full-text entities

- **Genes:** IGKV1D-16 (immunoglobulin kappa variable 1D-16) [NCBI Gene 28901] {aka IGKV1D16, L15, L15a}, NPPC (natriuretic peptide C) [NCBI Gene 4880] {aka CNP, CNP2}, FGFR3 (fibroblast growth factor receptor 3) [NCBI Gene 2261] {aka ACH, CD333, CEK2, HSFGFR3EX, JTK4}
- **Diseases:** dural tear (MESH:D020785), Achondroplasia (MESH:D000130), skeletal deformities (MESH:D009140), cardiac (MESH:D006331), LSM (MESH:D009800), exaggerated lumbar lordosis (MESH:D008141), infection (MESH:D007239), skeletal dysplasia condition (MESH:C535858), genu varum (MESH:D056305), cauda equina syndrome (MESH:D011128), hypotonia (MESH:D009123), spine malformations (MESH:D016135), back pain (MESH:D001416), central and obstructive sleep apnea (MESH:D020182), impaired mobility (MESH:D014086), bowel or bladder dysfunction (MESH:D001745), paraplegia (MESH:D010264), spinal cord compression (MESH:D013117), Spinal deformities (MESH:D013122), foramen magnum stenosis (MESH:D003251), claudication (MESH:D007383), sagittal deformity (MESH:D003398), spinal malalignment (MESH:D017760), TLK (MESH:D007738), Spinal stenosis (MESH:D013130), radiculopathy (MESH:D011843), lumbar stenosis (MESH:C563613), ear infections (MESH:D010031), impaired endochondral bone growth (MESH:D006130), sciatica (MESH:D012585), IPD (MESH:C535290), pain (MESH:D010146)
- **Chemicals:** Ascendis (-), Vosoritide (MESH:C000632572)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12954483/full.md

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Source: https://tomesphere.com/paper/PMC12954483