U.S., Jan. 31 -- ClinicalTrials.gov registry received information related to the study (NCT07378579) titled 'An Investigational Study to Evaluate the Cardiac Safety Assessment (TQTc Study) of ESK-001' on Dec. 10, 2025.

Brief Summary: This a phase 1, partially blinded, randomized, crossover study to determine the pharmacokinetics (PK) and QT/QTc interval of study drug (ESK-001) in healthy volunteer participants,

Study Start Date: June 21, 2024

Study Type: INTERVENTIONAL

Condition: Healthy Volunteer

Intervention: DRUG: ESK-001

Single oral dose of ESK-001 in participants

DRUG: Moxifloxacin (400 mg)

positive control

DRUG: Placebo

ESK-001-matched placebo

Recruitment Status: COMPLETED

Sponsor: Alumis Inc

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