Autosomal dominant hypocalcemia 1
MONDO:0011013Any autosomal dominant hypocalcemia in which the cause of the disease is a mutation in the CASR gene.
Also known as: hypocalcemia, autosomal dominant, CASR autosomal dominant hypocalcemia, HYPOC1, autosomal dominant hypocalcemia caused by mutation in CASR, autosomal dominant hypocalcemia type 1, hypocalcemia, autosomal dominant type 1, hypocalcemia, autosomal dominant, with Bartter syndrome, hypercalciuric hypocalcemia
7 clinical trials for this condition and its sub-types, 4 tagged with Autosomal dominant hypocalcemia 1 itself.
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New drug aims to fix calcium levels in rare genetic disease
Disease control OngoingThis study tests a new drug called encaleret against usual treatments for people with a rare genetic condition called autosomal dominant hypocalcemia type 1 (ADH1), which causes low blood calcium and high urine calcium. About 67 participants will receive either encaleret or stand…
Phase 3 • Sponsor: Calcilytix Therapeutics, Inc., a BridgeBio company • Aim: Disease control
Last updated Jul 31, 2026 00:00 UTC
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New study monitors rare calcium disorder to better understand its long-term effects
Knowledge-focused OngoingThis study is for people with autosomal dominant hypocalcemia types 1 or 2, rare genetic conditions that cause low blood calcium. Researchers will collect past and future health data from 95 participants to learn how the disease changes over time. The goal is to better understand…
Sponsor: Calcilytix Therapeutics, Inc., a BridgeBio company • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:25 UTC