An Efficacy and Safety Trial of Intravenous Zoledronic Acid in Infants Less Than One Year of Age, With Severe Osteogenesis Imperfecta

Shriners Hospitals for Children14 enrolled

Overview

The investigators have currently finished conducting an international multi-center trial that compares the efficacy and safety of pamidronate and zoledronate in the treatment of moderate to severe forms of Osteogenesis Imperfecta (OI). This trial has included only children above one year of age. The aim of the current study is to extend the observations of that currently finished study to infants below 1 year of age. Moreover, it is possible to administer zoledronate in a single short infusion instead of the three-day cycles with Pamidronate, therefore decreasing patient and family burdens with shorter stays in the hospital.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Osteogenesis Imperfecta

Interventions

Eligibility

Sex: ALLMax age: 12 Months

Medical Language ↔ Plain English

Inclusion Criteria: * Children, male or female 2 weeks to \< 12 months of age, at least at 38 weeks gestational age. * Any child with phenotypic OI type II, III or IV. * Any child classified as OI type I, V-VIII that has had at least two or more previous fractures of long bone, or vertebral compression fractures, and a low bone mineral density. * No previous treatment with bisphosphonates. * Negative urine protein as measured by dipstick. One repeat assessment of the urine protein will be allowed. Exclusion Criteria: * Blood oxygen saturation of less than 90% in room air. * Serum creatinine level greater than 56 µmol/L. * Any clinically significant clinical laboratory abnormalities at screening. * Treatment with any investigational drug within the past 30 days. * Patients who are unlikely to be able to complete the study or comply with the visit schedule. * Any disease or planned therapy which will interfere with the procedures or data collection of this trial.

Outcomes

Primary Outcomes

The primary objective of this trial is to assess the change in lumbar spine bone mineral density Z-score at month 24 relative to baseline in zoledronic acid treated infants compared to historical controls.

Time frame: 3 times during 10 visits within 2 years

Secondary Outcomes

To assess the effect of zoledronic acid on the number of clinical fractures &/or vertebral compressions that occur over a two year period compared to untreated historical controls in infants.