← Back to Search

Monoclonal Antibodies

Patients with XLH for Hypophosphatemia

Phase 4
Waitlist Available
Led By Karl L Insogna, M.D.
Research Sponsored by Yale University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2.5 months
Awards & highlights

Study Summary

This trial will test if a new treatment for XLH, Crysvita, can help improve symptoms of fatigue and weakness.

Eligible Conditions
  • Hypophosphatemia

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2.5 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 2.5 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Skeletal Muscle Adenosine Triphosphate (ATP) Synthesis Rate
Secondary outcome measures
Intracellular Phosphate Concentration in Umol/g Muscle
Serum Phosphate
Other outcome measures
Sit to Stand
Six-minute Walk Test
Timed up and go Test

Side effects data

From 2022 Phase 4 trial • 10 Patients • NCT04146935
10%
Partial ureteropelvic junction obstruction by staghorn calculus
100%
80%
60%
40%
20%
0%
Study treatment Arm
Patients With XLH

Trial Design

1Treatment groups
Experimental Treatment
Group I: Patients with XLHExperimental Treatment1 Intervention
Patients will receive Burosumab monthly at visits 1,2 and 3 subcutaneously at a dose of 1.0 mg/kg. Dose may be adjusted as needed.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Burosumab Injection [Crysvita]
2019
Completed Phase 4
~10

Find a Location

Who is running the clinical trial?

Yale UniversityLead Sponsor
1,854 Previous Clinical Trials
2,740,551 Total Patients Enrolled
3 Trials studying Hypophosphatemia
84 Patients Enrolled for Hypophosphatemia
Karl L Insogna, M.D.Principal InvestigatorYale University

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~2 spots leftby May 2025