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OpenTrials
Completed

NCT Number: NCT02587390

Effect of Gemcabene on the Pharmacokinetics of Simvastatin in Healthy Volunteers

The purpose of this study is to determine the effect of gemcabene on the pharmacokinetics of simvastatin 80 mg.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males and Females
  • >18 years of age
  • Body weight 45 kg or greater

Exclusion criteria

  • If female, of childbearing potential or lactation
  • History of significant adverse reaction to any fibrate lipid-lowering agent or HMG-CoA reductase inhibitor

Treatment and study plan

Gemcabene 900 mg

Drug

3x300 mg Gemcabene tablets orally once daily (QD) for 15 days

Simvastatin 80 mg

Drug

2x40 mg Simvastatin tablets orally once daily (QD) for 15 days

Primary outcomes

  1. Pharmacokinetics

    Time frame: 15 days

    Cmax

  2. Pharmacokinetics

    Time frame: 15 days

    Area Under the Curve (AUC)

Secondary outcomes

  1. Adverse Events

    Time frame: 57 days

  2. Clinical Laboratory - hematology, chemistry, urinalysis

    Time frame: 57 days

    Clinical Laboratory Abnormalities

  3. ECG

    Time frame: 57 days

    Clinically Significant Changes

Sponsors and collaborators

Lead sponsor

NeuroBo Pharmaceuticals Inc.

Industry

Registry information

Official study title

A Study to Evaluate the Effects of Gemcabene on the Steady-State Pharmacokinetics and Pharmacodynamics of Simvastatin in Healthy Volunteers

Important dates

Study start
2000
Primary completion
2000
Study completion
2000
First posted
Oct 27, 2015
Registry last updated
Apr 9, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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