Clinical Trials in the USA / NCT04783428
Active, not recruiting
Observational
Tumor-induced Osteomalacia Disease Monitoring Program
NCT04783428 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Tumor-induced Osteomalacia (TIO)
Investigational drug(s) / intervention(s)
No intervention
No intervention: Access to any treatment is through authorized commercial use and not as part of this DMP
Study summary
The objectives of this observational study are to assess the long-term safety and long-term effectiveness of burosumab in patients with TIO who are being treated with burosumab as prescribed by their physician and to monitor the course of the underlying phosphaturic mesenchymal tumor (PMT) overtime in patients with TIO irrespective of their treatment status.
Eligibility
Inclusion Criteria:
* Have a clinical diagnosis of TIO based on the presence of an underlying PMT (confirmed by imaging) AND/OR historical documentation. Note: For adult patients with TIO in whom the causative PMT has never been located, and all pediatric patients, documented evidence of negative genetic testing for other hereditary hypophosphatemic disorders is necessary
* For patient safety, all participating female patients of child-bearing potential must be willing to have pregnancy tests prior to certain assessments performed as part of the DMP
* Be willing to provide access to prior medical records including tumor pathology reports and biopsy slides, imaging, biochemical, and diagnostic, medical, and surgical history data, if available
* Be willing and able to provide informed consent after the nature of the study has been explained, and prior to any research-related procedures
* Be willing and able to comply with the study visit schedule and study procedures
Exclusion Criteria:
* Have a clinical diagnosis of TIO deemed to be caused by a tumor other than a PMT
* Serious medical or psychiatric comorbidity that, in the opinion of the Investigator, would present a concern for patient safety or compromise the ability to provide consent or comply with the study visit schedule and study procedures
* Less than 1 year of life expectancy (for any cause) in the opinion of the Investigator
* Concurrent enrollment in a clinical trial without prior approval from the TIO DMP Sponsor
* Undergoing treatment with burosumab for an unapproved indication
Primary outcome measure(s)
- Long-Term Effectiveness of Burosumab: Change From Baseline in Serum Phosporus Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change From Baseline in Serum 1,25(OH)2D Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change From Baseline in Serum Alkaline Phosphatase (ALP) Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change From Baseline in Serum FGF23 Over Time in Participants Not Undergoing Treatment With Burosumab — 10 years
- Long-Term Safety of Burosumab: Change From Baseline in Phosphaturic Mesenchymal Tumor (PMT) Size Over Time as Assessed by Tumor Imaging — 10 years
- Long-Term Safety of Burosumab: Number of Participants With New PMT Development as Assessed by Tumor Imaging — 10 years
- Long-Term Safety of Burosumab: Change From Baseline in Serum iPTH Over Time — 10 years
- Long-Term Safety of Burosumab: Change From Baseline in Serum Calcium Over Time — 10 years
- Long-Term Safety of Burosumab: Change From Baseline in Urine Calcium Over Time — 10 years
- Long-Term Safety of Burosumab: Change From Baseline Urinary Calcium/Creatinine Ratio — 10 years
- Long-Term Safety of Burosumab: Change From Baseline in Serum Creatinine Over Time — 10 years
- Long-Term Safety of Burosumab: Change From Baseline in Urine Creatinine Over Time — 10 years
- Long-Term Safety of Burosumab: Change From Baseline in Urine Protein/Creatinine Ratio Over Time — 10 years
- Long-Term Safety of Burosumab: Number of Participants With Nephrocalcinosis Over Time — 10 years
- Long-Term Safety of Burosumab: Number of Participants With Serious Adverse Events (SAEs) and Adverse Events (AEs) and Related AEs — 10 years
- Long-Term Safety of Burosumab: Number of Participants With Incidence and/or Progression of Spinal Stenosis Over Time — 10 years
- Long-Term Safety of Burosumab: Number of Participants With Normal and/or Potentially Clinically Significant Pregnancy Outcomes — 10 years
Includes maternal, neonatal and infant outcomes - Long-Term Effectiveness of Burosumab: Change From Baseline in Brief Fatigue Inventory (BFI) Scores in Adult Participants Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change From Baseline in Patient-Reported Outcomes Measurement Information System (PROMIS) Fatigue Scores in Pediatric Participants Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change From Baseline in Brief Pain Inventory (BPI) Scores in Adult Participants Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change From Baseline in PROMIS Pain Scores in Pediatric Participants Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change From Baseline in PROMIS Physical Function Scores Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change From Baseline in Short Form-36 version 2 (SF-36v2) in Adult Participants Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Change in Short Form-10 (SF-10) for Pediatric Participants Over Time — 10 years
- Long-Term Effectiveness of Burosumab: Number of Participants With Changes From Baseline in Clinical Findings — 10 years
- Long-Term Effectiveness of Burosumab: Number of Participants With Changes From Baseline in Resource/Health Utilization — 10 years
Trial sites (6)
| Facility | City | Region | Status |
|---|---|---|---|
| Yale University | New Haven | Connecticut | |
| Indiana University | Bloomington | Indiana | |
| Johns Hopkins University | Baltimore | Maryland | |
| Vanderbilt University Medical Center | Nashville | Tennessee | |
| University of Virginia | Charlottesville | Virginia | |
| IDIM - Instituto de Diagnóstico e Investigaciones Metabólicas | Buenos Aires | Argentina |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04783428 on ClinicalTrials.gov ↗ ← All trials in the USA