Clin2
NCT04987073Possibly a fitRecruiting

Vitamin D type added for CYP24A1 vitamin D deficiency

Idiopathic Infantile Hypercalcemia - Severe Form

Part of Genetic & congenital, Hormones & metabolism clinical trials.

This study tests a vitamin D-like medicine for people with a specific genetic cause of low active vitamin D (CYP24A1 deficiency). If you have the right gene change, it may help your body use vitamin D more normally.

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

Phase
N/A
Enrollment
30 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have a genetic test showing CYP24A1 has two changed copies (biallelic mutation)
  • You are able to give informed consent to join the study

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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