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Completed

NCT Number: NCT01487460

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TAP311 in Healthy Subjects and Dyslipidemic Patients

This study will assess the safety, tolerability, and effect of TAP311 on blood lipids in healthy subjects and in patients who have dyslipidemia. The effect of food on TAP311 concentration in blood and effect of TAP311 administration on simvastatin concentration will also be assessed in healthy volunteers.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Novartis Investigative Site

Miramar, Florida, 33025, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy male and female subjects age 18 to 65 years of age included, and in good health as determined by past medical history, physical examination, electrocardiogram, and laboratory tests at screening.
  • OR untreated dyslipidemic patients.
  • Subjects must weigh at least 50 kg to participate in the study, and must have a body mass index (BMI) within the range of 18 - 36 kg/m2.
  • Able to communicate well with the investigator, to understand and comply with the requirements of the study.

Exclusion criteria

  • Use of other investigational drugs at the time of enrollment.
  • Active treatment for type 1 diabetes or type 2 diabetes mellitus.
  • A past medical history of ECG abnormalities, documented cardiac arrhythmias or cardiovascular diseases.
  • History of malignancy of any organ system, treated or untreated, within the past 5 years.
  • Pregnant or nursing (lactating) women.
  • Smokers.
  • Use of any prescription drugs, herbal supplements and/or over-the-counter (OTC) medication, dietary supplements.
  • History of drug or alcohol abuse within the 12 months prior to dosing.
  • Any surgical or medical condition, acute or unstable chronic disease which may, based on the investigator's opinion, jeopardize the patient in case of participation in the study

Other protocol-defined inclusion/exclusion criteria may apply.

Treatment and study plan

TAP311

Drug

Primary outcomes

  1. Safety and tolerability of single and multiple doses of TAP311 in healthy subjects and patients with dyslipidemia

    Time frame: Up to 21 days

    Number of patients with adverse events and changes from baseline in vital signs, ECG and clinical labs (blood chemistry, hematology and urinalysis).

Secondary outcomes

  1. TAP311 concentrations in blood and urine following administration of single and multiple doses in healthy subjects and in patients with dyslipidemia.

    Time frame: 25 timepoints over 17 days

  2. Effect of TAP311 administration on simvastatin (and metabolite) blood concentration in healthy subjects.

    Time frame: 10 days

    Simvastatin (and metabolite) blood concentration before and after TAP311 treatment.

  3. Effect of food on TAP311 blood concentration in healthy subjects.

    Time frame: 3 days

    TAP311 blood concentration when the drug is administered with and without food.

  4. Effects of TAP311 on total cholesterol in patients with dyslipidemia

    Time frame: 8 timepoints over 15 days

    Total cholesterol blood concentration before and after TAP311 treatment.

  5. Effects of TAP311 on Low Density Lipoprotein (LDL-C) in patients with dyslipidemia

    Time frame: 8 timepoints over 15 days

    LDL-C blood concentration before and after TAP311 treatment.

  6. Effects of TAP311 on high density lipoprotein (HDL-C)in patients with dyslipidemia.

    Time frame: 8 timepoints over 15 days

    HDL-C blood concentration before and after TAP311 treatment.

  7. Effects of TAP311 on triglycerides in patients with Dyslipidemia

    Time frame: 8 timepoints over 15 days

    Triglycerides concentration in blood before and after TAP311 treatment.

Sponsors and collaborators

Lead sponsor

Novartis Pharmaceuticals

Industry

Registry information

Official study title

A First-in-human Randomized, Double-blind, Placebo-controlled, 4-part Study to Assess Safety, Tolerability, Pharmacokinetics (Including Open Label Study of Food Effect and Interaction With Simvastatin) and Pharmacodynamics of Interwoven Single- and Multiple-ascending Doses of TAP311 in Healthy Subjects and Dyslipidemic Patients.

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Dec 7, 2011
Registry last updated
Dec 21, 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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