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Starting soon Phase 1

A Phase 1 Clinical Trial to Evaluate the Safety and the Pharmacokinetic Drug-Drug Interaction Between HUC2A-752-A and HUC2A-752-B in Healthy Adults

NCT07784621 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 1
Started
2026-10
Last updated
2026-09-10

Condition(s) studied

Hypertension

Investigational drug(s) / intervention(s)

Losartan (COZZAR®) →Pitavastatin plus EzetemibeAll Pitavastatin trials (6) →All Ezetemibe trials (2) →

Losartan (COZZAR®): HUC2A-752-A

Pitavastatin plus Ezetemibe: HUC2A-752-B

Study summary

This study evaluates the pharmacokinetic drug-drug interactions of repeated co-administration of HUC2A-752-A and HUC2A-752-B compared to monotherapy of each agent in healthy adults

Eligibility

Sex
ALL
Min age
19 Years
Max age
64 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy adult volunteers * Individuals with a body weight between 50.0 kg and 90.0 kg and a BMI between 18.5 kg/m² and 29.9 kg/m² Exclusion Criteria: * Individuals with a history or presence of clinically significant diseases of the following systems: hepatobiliary, renal, neurological, immunological, respiratory, gastrointestinal, endocrine, hematologic/oncologic, cardiovascular , musculoskeletal, urological, psychiatric, or sexual dysfunction. * Individuals with a history of gastrointestinal diseases or gastrointestinal surgeries that could affect the safety or pharmacokinetic evaluation of the investigational product. * Individuals with a history of hypersensitivity or clinically significant hypersensitivity reactions to losartan, pitavastatin, ezetimibe, angiotensin receptor blockers, statins, or any other medications.

Primary outcome measure(s)

  • AUCtau,ss — Day 15
    Area Under the Curve
  • Cmax,ss — Day 15
    Maximum concentration at steady state

Trial sites (1)

FacilityCityRegionStatus
Seoul National University Hospital Seoul Jongno-gu
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07784621 on ClinicalTrials.gov ↗ ← All trials in South Korea