A PHASE 3, OPEN-LABEL, LONG-TERM EXTENSION STUDY TO EVALUATE THE SAFETY AND EFFICACY OF VOSORITIDE IN CHILDREN WITH HYPOCHONDROPLASIA

Registry ID

111-308

Source registry

HEALTH_CANADA

Status

Ongoing

Phase

PHASE3

Study type

INTERVENTIONAL

Sponsor

BIOMARIN PHARMACEUTICAL INC

Start date

2025-09-09

Last update

2025-06-13

Conditions

• HYPOCHONDROPLASIA

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• A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF VOSORITIDE IN CHILDREN WITH HYPOCHONDROPLASIA.

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