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Vosoritide

CNP analogue

Vosoritide é um análogo de CNP avaliado em ensaios clínicos de acondroplasia, incluindo um estudo fase 3 randomizado e controlado por placebo.[1]

Reviewed 2026-09-02

01 / Overview

Quick facts

Somente campos atualmente documentados aparecem neste registro.

class
CNP analogue
molecule Type
Peptide analogue
primary Target
Growth plate chondrocytes
receptor
NPR-B
primary Axis
CNP / cGMP
research Status
Approved drug
developer
BioMarin

What is it studied for?

established
Annualized growth velocity in children with achondroplasia

Evaluated in a 52-week phase 3 randomized, double-blind, placebo-controlled trial.

02 / Mechanism

Mechanism of action

Fluxo estruturado para navegação. Uma seta indica sequência conceitual, não necessariamente interação direta.

Vosoritide
NPR-BcGMP
Modulation of FGFR3 downstream signaling
Endochondral bone growth

03 / Evidence synthesis

What does the evidence actually show?

As categorias evitam misturar evidência humana, dados pré-clínicos e plausibilidade mecanística. A cobertura desta versão não é uma revisão sistemática.

established
  • The phase 3 trial found a greater change in annualized growth velocity at 52 weeks than placebo.
supported

Data not indexed yet.

preliminary
  • The trial did not establish final adult height or long-term harms.
preclinical

Data not indexed yet.

mechanistic

Data not indexed yet.

Unsupported / exaggerated

Claims review not indexed yet.

04 / Published protocols

Dosing reported in published human studies

The values reproduce protocols described in published research. They are not recommendations, prescriptions or clinical guidance.

Dosing reported in published human studies
StudyPopulationNRouteDose reportedFrequencyDurationDesignPrimary outcomeReference
Ravi Savarirayan et al.Ambulatory children aged 5 to <18 years with achondroplasia121Subcutaneous15.0 µg/kgOnce daily52 weekshuman-rct · not-extractedChange from baseline in annualized growth velocity at 52 weeksOpen

06 / Safety

Safety & Adverse Events

Reported findings

  • Adverse events were common in both study groups; no serious adverse event was considered treatment-related in the trial report.

Pharmacological concerns

Data not indexed yet. Lack of indexed harm data is not evidence of safety.

Unknowns

  • Final adult height and long-term harms were not established by the 52-week study.

07 / Source literature

Studies

1 indexed

Multiple entry points

Related Paths

Vosoritide can also be explored through these curated graph routes.

No dead ends

Continue Exploring

09 / References

References

  1. [1]

    Ravi Savarirayan, Louise Tofts, Melita Irving, William Wilcox, Carlos A. Bacino, et al.. Once-daily, subcutaneous vosoritide therapy in children with achondroplasia: a randomised, double-blind, phase 3, placebo-controlled, multicentre trial. The Lancet. 2020.