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NCT Number: NCT07375290

Zoledronate to Prevent Bone Health Complications in Pediatric Hematopoietic Stem Cell Transplant Survivors

The purpose of this pilot study is to investigate the safety and preliminarily assess efficacy of early intervention with zoledronate in high risk pediatric hematopoietic stem cell transplantation (HSCT) patients to prevent the development of bone disease and fractures and reduce potential pain and suffering.

Recruiting

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Key information

Age range

5 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, 45229, United States

Location status: Recruiting

Location contact

Jessi Anderson

CONTACT

[email protected]

Jonathan Howell, MD

PRINCIPAL_INVESTIGATOR

About this study

Bone disease, including low bone density and fragility fractures (osteoporosis), is common among survivors of pediatric hematopoietic stem cell transplantation (HSCT). Further, patients who develop graft-versus-host disease (GVHD) following HSCT or who have high cumulative doses of glucocorticoids are at even higher risk to develop bone complications. Recent data also suggest that a large number of HSCT candidates arrive to transplantation already with low bone mineral density, adding to the potential risk of developing bone disease following HSCT. Typically, treatment for osteoporosis in children using bisphosphonates, such as zoledronate, is recommended only after the development of fragility fractures.

The investigators propose to study the safety and efficacy of a novel method of early intervention with zoledronate in high risk pediatric HSCT patients to prevent the development of bone disease and fractures in order to reduce potential pain and suffering.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients ≥5 and ≤18 years old who are preparing for HSCT with a height-for-age corrected DXA Z-score of <-2.0 and admitted to a CCHMC inpatient unit.
  • Patients ≥5 and ≤18 years old recovering from HSCT and who have developed de novo acute or chronic GVHD and are admitted to a CCHMC inpatient unit.

Exclusion criteria

  • Age <5 years and >18 years
  • Patients with Fanconi anemia or other radiation-sensitive syndromes with increased malignancy risk
  • history of prior bisphosphonate use
  • low 25-OH vitamin D levels (<20 ng/mL)
  • active febrile illness
  • uncontrolled infection
  • Elevated creatinine at the time of enrollment, history or renal failure, or documented low glomerular filtration rate (GFR≤90)
  • Active bone disease including history of abnormal PTH level for any reason, active bone fracture/healing, or primary disorder of bone development or metabolism.
  • Women who are pregnant or breast feeding.

Treatment and study plan

Zoledronate

Drug

Zoledronate is in the class of drugs entitled bisphosphonates which act to inhibit bone resorption by inhibiting osteoclast activity therefore reducing bone turnover.

Primary outcomes

  1. Safety of early intervention Zoledronate

    Time frame: At the time of infusion through up to 60 days post last dose of Zoledronate

    Calcium levels following infusion of zoledronate

  2. Feasibility of early intervention Zoledronate

    Time frame: At patient discharge, typically 1 week post infusion

    Number of days required for inpatient stay beyond what is necessary for the patient's admission

Secondary outcomes

  1. Bone health efficiency

    Time frame: Baseline, +6 months, and +12 months

    DXA scans will be measured with a z-score comparing bone density to averages for patient age and height

  2. Bone substrate turnover

    Time frame: Baseline and +30 days

    c-terminal telopeptide (CTX) and procollagen type 1 n-terminal propeptide (P1NP) measured in pg/mL

Study contacts

Contact information is provided by the study sponsor or research team.

Brady Landon

CONTACT

[email protected]

Jessi Anderson

CONTACT

[email protected]

513-803-0177

Sponsors and collaborators

Lead sponsor

Children's Hospital Medical Center, Cincinnati

Other

Registry information

Official study title

Early Intervention With Zoledronate to Safely Prevent Bone Health Complications in Pediatric Hematopoietic Stem Cell Transplant Survivors

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jan 29, 2026
Registry last updated
Jan 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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