Phase 3Active, not recruiting

Efficacy and Safety of Encaleret Compared to Standard of Care in Participants With ADH1 (CALIBRATE)

CALIBRATE: A Phase 3, Randomized, Open-Label Study Evaluating the Efficacy and Safety of Encaleret Compared to Standard of Care in Participants With Autosomal Dominant Hypocalcemia Type 1 (ADH1)

Sponsor
Calcilytix Therapeutics, Inc., a BridgeBio company (Industry)
Enrollment
67 enrolled
Conditions
Autosomal Dominant Hypocalcemia (ADH)
Interventions
Encaleret; Standard of Care
Ages
children, adults, older adults
Registry
NCT05680818

Full record on ClinicalTrials.gov

From the registry

The primary purpose of the study is to understand the effectiveness, safety, and tolerability of encaleret when compared to standard of care (SoC) treatment in participants with Autosomal Dominant Hypocalcemia Type 1 (ADH1).

Primary outcomes

  • Number of Responders who Achieve Both Albumin-Corrected Blood Calcium (cCa) and 24-hour Urinary Calcium (UCa) Within the Target Range

History

  1. Study completion expected

  2. Last registry update

  3. Primary completion

  4. Registered

  5. Started