Clin2
NCT07080385Possibly a fitRecruiting

Study of encaleret in children with a rare calcium disorder

Autosomal Dominant Hypocalcemia Type 1 (ADH1)

Part of Hormones & metabolism clinical trials.

This trial tests a medicine called encaleret in children with a rare genetic condition that causes low calcium levels. The goal is to see if it safely helps control calcium and reduce symptoms.

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

Phase
Phase 2/Phase 3
Enrollment
28 people
Ages
birth to 17 years
Study type
Interventional

Who can take part

  • You must have a confirmed genetic change in the calcium-sensing receptor (CASR) that causes low calcium or low parathyroid hormone (PTH).
  • You must have at least one symptom or sign of hypoparathyroidism (low calcium).
  • You must have been on treatment for this condition for at least 3 to 6 months before joining.
  • You must not have had thyroid or parathyroid surgery.
  • You must not have had a kidney transplant.
  • You cannot take certain heart medicines or strong interacting drugs for a period before starting.

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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