Clin2
NCT03301038Possibly a fitRecruiting

Rifampin for a rare calcium disorder caused by CYP24A1

Idiopathic Infantile Hypercalcaemia - Severe FormGenetic DiseaseHypercalcemia, Idiopathic, of InfancyHypercalciuric HypercalcemiaIdiopathic Infantile Hypercalcemia - Mild FormHypercalciuria

Treatments studied

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

This trial tests rifampin to improve high blood and/or urine calcium that happens in people with CYP24A1 gene changes. It also checks safety by watching liver and kidney blood tests and pregnancy status.

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

Phase
Phase 2
Enrollment
60 people
Ages
6 months to 65 years
Study type
Interventional

Who can take part

  • You are between 6 months and 65 years old
  • You have at least one known CYP24A1 gene mutation
  • Your blood and/or urine calcium is higher than normal for your age
  • Your parathyroid hormone (PTH) blood test is below 20 pg/mL
  • Your vitamin D level called 1,25-dihydroxy vitamin D3 is elevated or normal
  • You are able and willing to follow study visits and procedures

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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