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NCT06785454

A Study to Assess the Efficacy and Safety of Lorundrostat in Participants With Obstructive Sleep Apnea and Hypertension

Completed Phase 2 Last updated 13 January 2026
What this trial tests

Phase 2 trial testing Lorundrostat in Obstructive Sleep Apnea in 48 participants. Completed in 29 December 2025.

Timeline
28 February 2025
Primary endpoint
17 December 2025
29 December 2025

Quick facts

Lead sponsorMineralys Therapeutics Inc.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposetreatment
Enrollment48
Start date28 February 2025
Primary completion17 December 2025
Estimated completion29 December 2025
Sites27 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Mineralys Therapeutics Inc. — full company profile →

Who can join

Adults 18 to 75, any sex, with Obstructive Sleep Apnea or Hypertension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary purpose of the study is to assess the effect of lorundrostat taken orally (po) once a day on the Apnea-Hypopnea Index (AHI) in participants with moderate to severe obstructive sleep apnea (OSA) and hypertension.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Obstructive Sleep Apnea

Currently open trials in the same condition.

Other Mineralys Therapeutics Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06785454.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing