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Bone Health
Clinical

Vosoritide

Also known as: Voxzogo, BMN 111

A C-type natriuretic peptide analog FDA-approved as Voxzogo to increase linear growth in children with achondroplasia. Prescription.

Last updated

Mechanism of Action

Vosoritide is a 39-amino-acid analog of C-type natriuretic peptide (CNP) modified to resist breakdown by neutral endopeptidase. It binds natriuretic peptide receptor B (NPR-B) on growth-plate chondrocytes, raising intracellular cGMP. This dampens the overactive FGFR3 signaling through the MAPK (RAF-1/MEK/ERK) pathway that causes achondroplasia, allowing more chondrocyte proliferation and endochondral bone growth.

Half-life
~21-28 minutes
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Increases annualized growth velocity in children with achondroplasia (phase 3)
  • Growth gains sustained in multi-year extension studies
  • Studied in infants and young children with achondroplasia
  • Increased growth velocity in a phase 3 hypochondroplasia trial (2026)

Potential Side Effects

  • Injection-site reactions (redness, swelling, bruising)
  • Transient decreases in blood pressure, dizziness and fatigue
  • Vomiting and nausea
  • Arthralgia

Common Dosing

Labeled dosing is a weight-based subcutaneous injection once daily, given by a caregiver after training, with adequate food and fluid beforehand to reduce the risk of low blood pressure. Treatment continues only while growth plates remain open. Dosing is set and supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • Closed epiphyses (no benefit once growth plates close)
  • Significant cardiac disease or low blood pressure: use with caution
  • Severe kidney impairment (not studied)

No documented stacking partners for Vosoritide yet.

  • Once-daily, subcutaneous vosoritide therapy in children with achondroplasia: a randomised, double-blind, phase 3, placebo-controlled, multicentre trial

    2020

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  • Vosoritide therapy in children with achondroplasia aged 3-59 months: a multinational, randomised, double-blind, placebo-controlled, phase 2 trial

    2024

    View
  • A Phase 3 Trial of Vosoritide in Children with Hypochondroplasia

    2026

    View

Yes. The FDA granted accelerated approval to Voxzogo in November 2021 for children 5 and older with achondroplasia and open growth plates, and extended it in October 2023 to children of all ages. As of 2026, BioMarin has filed for full approval in achondroplasia and for hypochondroplasia, with those applications under FDA review.

Trials show increased growth velocity and height gains over several years of treatment, but data on final adult height are still accumulating. Benefit depends on starting while growth plates are open.

No. It mimics C-type natriuretic peptide and acts directly on growth-plate cartilage to counter the FGFR3 mutation behind achondroplasia, rather than raising growth hormone or IGF-1.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.