Interventional Study of Vosoritide for the Treatment of Children With Hypochondroplasia

Hypochondroplasia Clinical Trial

Official title:

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Vosoritide in Children With Hypochondroplasia

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT06455059
• Other study ID #: 111-303
• Status: Enrolling by invitation
• Phase: Phase 3
• Start date: June 1, 2024
• Est. completion date: August 1, 2026

Study information

• Verified date: June 2024
• Source: BioMarin Pharmaceutical
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The intent and design of this Phase 3 study is to assess vosoritide as a therapeutic option for the treatment of children with hypochondroplasia (HCH).

Description:

This is a Phase 3 randomized, stratified, placebo-controlled, double-blind multicenter study to evaluate the effect of 52 weeks of daily vosoritide administration on annualized growth velocity (AGV) in participants with HCH. Eligible participants with documented HCH confirmed by genetic testing will roll over from Study 111-902 and enter the 111-303 study. Participants will be randomly assigned to one of two treatment groups: Placebo or Vosoritide. The route of administration is subcutaneous injection, and the frequency of administration is daily.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 80
• Est. completion date: August 1, 2026
• Est. primary completion date: August 1, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 3 Years to 17 Years

Eligibility

Inclusion Criteria:

1. Participants must be = 3 to < 18 years of age at enrollment

2. A confirmed genetic diagnosis of HCH

3. A height Z score of = - 2.0 standard deviations (SDs) in reference to the general population of the same age and sex, as calculated using the Center for Disease Control and Prevention (CDC) growth charts

4. Males and females are eligible to participate in this clinical study.

5. Females = 10 years old or who have begun menses must have a negative pregnancy test at the Screening Visit and be willing to have additional pregnancy tests during the study.

6. If sexually active, participants must be willing to use a highly effective method of contraception while participating in the study.

Exclusion Criteria:

1. Short stature condition other than HCH

2. Have an unstable condition likely to require surgical intervention during the study.

3. Evidence of decreased growth velocity and/or growth plate closure

4. Taking any of the prohibited medications

5. Treated with growth hormone, insulin-like growth factor 1 (IGF-1), or anabolic steroids

6. Planned or expected to have limb-lengthening surgery during the study period.

7. Planned or expected bone-related surgery (ie, surgery involving disruption of bone cortex, excluding tooth extraction), during the study period

8. Require any investigational agent prior to completion of study period.

9. Received vosoritide or another investigational product or investigational medical device in the past

10. Have used any investigational product or investigational medical device for the treatment of HCH or short stature at any time, including vosoritide

11. Have current malignancy, history of malignancy, or currently under work-up for suspected malignancy.

12. Have known hypersensitivity to vosoritide or its excipients.

13. Concurrent disease or condition that, in the view of the investigator, would interfere with study participation or safety evaluations, for any reason.

Related Conditions & MeSH terms

• Dwarfism
• Hypochondroplasia
• Lordosis

Intervention

Drug:
• Vosoritide
Subcutaneous injection of recommended dose of vosoritide based on weight-band dosing once daily.
• Placebo
Subcutaneous injection of recommended dose of placebo

Locations

Country	Name	City	State
Australia	Murdoch Children's Research Institute	Parkville	Victoria
United States	Children's National Medical Center	Washington	District of Columbia

Sponsors (1)

Lead Sponsor	Collaborator
BioMarin Pharmaceutical

Countries where clinical trial is conducted

United States,  Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from baseline in annualized growth velocity (AGV) at Week 52 versus placebo		At week 52
Secondary	Change from baseline in standing height at Week 52 versus placebo		At week 52
Secondary	Change from baseline in height Z-score at Week 52 versus placebo		At week 52