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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Notify MeKey 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 - high dose
DrugPlacebo
DrugPrimary outcomes
-
Assessment of tolerability by investigator on a 4-point scale
Time frame: Up to day 14 after drug administration
-
Number of subjects with adverse events
Time frame: Up to day 14 after drug administration
-
Number of subjects with clinically relevant findings in electrocardiogram (ECG)
Time frame: Up to day 14 after drug administration
-
Number of subjects with clinically relevant findings in vital signs
Time frame: Up to day 14 after drug administration
systolic and diastolic blood pressure
-
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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