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Completed

NCT Number: NCT01050127

A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of ABT-436 in Healthy Adults

The objectives of this study are to assess the safety, tolerability, pharmacodynamics and pharmacokinetics of multiple doses of ABT-436 in healthy adults.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Site Reference ID/Investigator# 24849

Waukegan, Illinois, 60085, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age is between 18 and 55 years, inclusive.
  • If female, subject must be postmenopausal for at least two years or surgically sterile.
  • Females must have negative results for pregnancy tests prior to study drug administration.
  • If male, subject must be surgically sterile or agree to be sexually inactive or agree to use a barrier method of birth control.
  • Body Mass Index is 18.0 to 29.9 kg/m2 (2 = superscript number), inclusive.
  • A condition of general good health based upon the results of a medical history, physical examination, vital signs, laboratory profile, and a 12-lead electrocardiogram.
  • Must voluntarily sign and date an informed consent, approved by an Independent Ethics Committee (IEC)/Institutional Review Board (IRB), prior to the initiation of any screening or study-specific procedures.

Exclusion criteria

  • History of significant sensitivity or allergy to any drug.
  • Use of known inhibitors or inducers of CYP3A within 30 days prior to the first dose of study drug and through the end of the study.
  • Requirement for, or use of within the 2-week period prior to study drug administration, any over-the-counter or prescription medication, vitamins, minerals or herbal supplements on a regular basis.
  • Receipt of any depot drug by injection within 30 days prior to study drug administration.
  • Positive screen for drugs of abuse or alcohol, or recent (6-month) history of drug or alcohol abuse.
  • Use of tobacco or other nicotine-containing products within the six-month period preceding study drug administration.
  • Donation or loss of 550 mL of blood or more (including plasmapheresis) or receipt of a transfusion of any blood product within 8 weeks prior to the first dose of study drug.
  • Receipt of an investigational product within a time period equal to 10 half-lives, if known, or a minimum of 6 weeks prior to study drug administration.
  • Has a clinically significant abnormal diastolic blood pressure (< 45 or > 90 mm Hg), systolic blood pressure (< 85 or > 140 mm Hg) or heart rate (< 45 or > 100 bpm).
  • HbA1c > 6.0%.

Treatment and study plan

ABT-436

Drug

See Arm Description for details.

Placebo

Drug

See Arm Description for details.

Primary outcomes

  1. Safety and Tolerability Assessments (i.e., electrocardiogram(ECG), clinical laboratory tests, vital signs, weight, adverse events (AE) assessment, pulmonary function tests, physical and brief neurological examinations)

    Time frame: Days -2 through Day 7 or 14

  2. Assess Pharmacokinetics (i.e., ABT-436 and possible metabolite levels)

    Time frame: Day -1 through Day 7

  3. Pharmacodynamics (i.e., biomarkers of drug effect)

    Time frame: Day -1 through Day 7

Sponsors and collaborators

Lead sponsor

Abbott

Industry

Registry information

Important dates

Study start
2009
Primary completion
2010
First posted
Jan 15, 2010
Registry last updated
Nov 3, 2010

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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