Clin2
NCT03775187Worth exploringAvailable

Expanded access to burosumab for x-linked hypophosphatemia

X-linked HypophosphatemiaTumor-Induced Osteomalacia

Part of Bones, joints & muscles, Genetic & congenital, Hormones & metabolism, Kidney & urinary, Women’s health & pregnancy clinical trials.

This program provides access to a medication called burosumab (Crysvita) for people with a rare genetic condition called X-linked hypophosphatemia (XLH), which causes weak bones and low phosphate levels. It is designed for those who cannot get the drug through normal channels or other clinical trials.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Ages
Any age
Study type
Expanded Access

Who can take part

  • You have a condition called X-linked hypophosphatemia (XLH), a rare genetic disorder that causes low phosphate levels in the blood.
  • You are not able to get burosumab (also known as Crysvita) through a regular prescription or other clinical trial.
  • You have a healthcare provider who is willing to request this medication for you through the expanded access program.
  • You are not currently enrolled in another investigational treatment for the same condition.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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