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OpenTrials
Completed

NCT Number: NCT02232542

Tolerability and Safety of Duloxetine BID in Healthy Female Subjects

Study to assess the safety and tolerability of 100 mg of duloxetine BID compared to 40 mg of duloxetine BID or placebo for 7 days

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Key information

Conditions

Age range

40 year and older

Sex eligibility

Female

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

  • Healthy female subjects as determined by results of screening
  • Signed written informed consent in accordance with Good Clinical Practice (GCP) and local legislation
  • Age ≥ 40 years
  • BMI ≥ 18.5 and ≤ 29.9 kg/m2

Exclusion criteria

  • Any finding at any of the medical examinations (including blood pressure, pulse rate and ECG (electrocardiogram)) deviating from normal and of clinical relevance (resting heart rate greater than 100 bpm or tachyarrhythmia)
  • History of or current gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunologic, hormonal disorders (except thyroid hormones and hormonal replacement therapy)
  • History of relevant orthostatic hypotension, fainting spells and blackouts
  • Diseases of the central nervous system (such as epilepsy) or psychiatric disorders
  • Chronic or relevant acute infections
  • History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator, any bleeding disorder including prolonged or habitual bleeding, other hematologic disease, cerebral bleeding (e.g. after a car accident), commotio cerebri
  • Intake of drugs with a long half-life (> 24 hours) within 1 month prior to administration
  • Use of any drugs that might influence the results of the trial (especially CYP2D6 or CYP1A2 modulating substances) within 2 weeks prior to administration or during the trial
  • Participation in another trial with an investigational drug within 2 months prior to administration or during trial
  • Smoker (> 10 cigarettes or 3 cigars or 3 pipes/day) or inability to refrain from smoking on study days
  • Alcohol abuse (> 60 g/day)
  • Caffeine abuse (> 4 cups/day)
  • Drug abuse
  • Blood donation within 1 month prior to administration or during the trial
  • Excessive physical activities within 10 days prior to administration or during the trial
  • Any laboratory value outside the clinically accepted reference range
  • Ineffective contraception

Treatment and study plan

Duloxetine - low dose

Drug

Duloxetine - high dose

Drug

Placebo

Drug

Primary outcomes

  1. Assessment of tolerability by investigator on a 4-point scale

    Time frame: Up to day 14 after drug administration

  2. Number of subjects with adverse events

    Time frame: Up to day 14 after drug administration

  3. Number of subjects with clinically relevant findings in electrocardiogram (ECG)

    Time frame: Up to day 14 after drug administration

  4. Number of subjects with clinically relevant findings in vital signs

    Time frame: Up to day 14 after drug administration

    systolic and diastolic blood pressure

  5. Number of subjects with abnormal changes in laboratory parameters

    Time frame: Up to day 14 after drug administration

Sponsors and collaborators

Lead sponsor

Boehringer Ingelheim

Industry

Registry information

Official study title

Tolerability and Safety of 40 mg and 100 mg Duloxetine BID Given Over 7 Days in Healthy Female Subjects. A Randomised, Placebo-controlled Double-blind Trial.

Important dates

Study start
2003
Primary completion
2003
First posted
Sep 5, 2014
Registry last updated
Sep 5, 2014

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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