RecruitingPhase 1NCT07726368

Study of ECC4703 With Sulfasalazine and Pitavastatin

A Phase 1, Open-Label, Fixed-Sequence, Single-Center, Two-Period, Drug-Drug Interaction Trial in Healthy Adult Participants to Evaluate the Effect of Steady-State ECC4703 on the Pharmacokinetics of Sulfasalazine (BCRP Probe Substrate) and Pitavastatin (OATP1B1/OATP1B3 Probe Substrate)


Sponsor

Eccogene

Enrollment

40 participants

Start Date

Aug 7, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Non-alcoholic fatty liver disease is a chronic, serious, life-threatening, inflammatory liver disease characterized by increased liver fat content, inflammation, and progressive fibrosis. The overall prevalence of non-alcoholic fatty liver disease is rapidly rising world-wide. ECC4703 is a potential new treatment for non-alcoholic fatty liver disease. The purpose of this research is to investigate the safety, tolerability and pharmacokinetics of sulfasalazine and pitavastatin when combined with ECC4703.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called ECC4703, a drug called Pitavastatin, and others for people with dyslipidaemia and non-alcoholic fatty liver disease nafld. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGECC4703

ECC4703 will be administered orally.

DRUGSulfasalazine

Sulfasalazine will be administered orally.

DRUGPitavastatin

Pitavastatin will be administered orally.


Locations(1)

Nucleus Network Pty Ltd

Melbourne, Victoria, Australia

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NCT07726368


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