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OpenTrials
Completed

NCT Number: NCT03927677

The Effect of Colchicine on the Pharmacokinetic Profile of LC350189 in Healthy Aldults.

This is a Phase 1, open-label, fixed-sequence, 3-period, 2-way drug interaction study designed to assess the PK, PD, safety, and tolerability of LC350189 and colchicine when administered alone and in combination in healthy subjects.

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • The subject is male or female 18 to 50 years of age, inclusive.
  • The subject has a body mass index 18 to 32 kg/m2, inclusive, at screening.
  • The subject is judged by the investigator to be in good general health, as determined by medical history, clinical laboratory assessments, vital sign measurements, 12 lead electrocardiogram (ECG) results, and physical examination findings at screening.
  • The subject agrees to comply with all protocol requirements.
  • The subject is able to provide written informed consent.

Exclusion criteria

  • The subject has a medical history with any issues affecting absorption or metabolism, as judged by the investigator.
  • The subject has a positive test result for hepatitis B surface antigen, hepatitis C virus antibody, or human immunodeficiency virus types 1 or 2 antibodies at screening.
  • The subject has used any prescription (excluding hormonal birth control and hormone replacement therapy) or over the counter medications (except paracetamol [up to 2 g per day]), including herbal or nutritional supplements, within 14 days before the first dose of study drug or throughout the study.
  • The subject has consumed grapefruit or grapefruit juice, Seville orange or Seville orange containing products (eg, marmalade), or caffeine- or xanthine containing products within 48 hours before the first dose of study drug or throughout the study.
  • The subject is a smoker or has used nicotine or nicotine-containing products (eg, snuff, nicotine patch, nicotine chewing gum, mock cigarettes, or inhalers) within 6 months before the first dose of study drug.
  • The subject has a history of alcohol abuse or drug addiction within the last year or excessive alcohol consumption (regular alcohol intake >21 units per week for male subjects and >14 units of alcohol per week for female subjects) (1 unit is equal to approximately ½ pint [200 mL] of beer, 1 small glass [100 mL] of wine, or 1 measure [25 mL] of spirits).
  • The subject has a positive test result for drugs of abuse, alcohol, or cotinine (indicating active current smoking) at screening or before the first dose of study drug.
  • The subject is a female who is pregnant, planning to become pregnant within the next 6 months, or currently breastfeeding.
  • In the opinion of the investigator, the subject is not suitable for entry into the study.

Treatment and study plan

Xanthine Oxidase Inhibitor

Drug

LC350189 200mg qd

Other names: LC350189

Primary outcomes

  1. Maximun observed concentration (Cmax) of LC350189 and Colchicine from plasma

    Time frame: from baseline up to Day 21

    Pharmacokinetic

  2. Area under the concentration-time curve (AUC) of LC350189 and Colchicine from plasma

    Time frame: from baseline up to Day 21

    Pharmacokinetic

  3. 3.Apparent terminal half-life (t1/2) of LC350189 and Colchicine from plasma

    Time frame: from baseline up to Day 21

    Pharmacokinetic

Secondary outcomes

  1. Incidence of Adverse events

    Time frame: from baseline up to Day 21

    Safety

  2. Changes in uric serum acid

    Time frame: from baseline up to Day 19

    Pharmacodynamic

Sponsors and collaborators

Lead sponsor

LG Chem

Industry

Registry information

Official study title

A Phase 1, Open-label, Fixed-sequence, 2-way Drug Interaction Study to Evaluate the Effect of Colchicine on the Pharmacokinetics of LC350189 and the Effect of LC350189 on the Pharmacokinetics of Colchicine in Healthy Subjects

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Apr 25, 2019
Registry last updated
Jun 26, 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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