Pharmacokinetic Study Of AGILE AG200-15 After Weekly Application Under Various Conditions in Healthy Female Volunteers
| Status: | Completed |
|---|---|
| Conditions: | Healthy Studies |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 18 - 45 |
| Updated: | 8/2/2018 |
| Start Date: | May 2011 |
| End Date: | June 2011 |
A Pharmacokinetic And Wearability Study of the Agile TCDS AG200-15 Following Weekly Application Under Various External Conditions in Healthy Female Volunteers
A study to evaluate pharmacokinetic profile, wearability and safety of AG200-15, transdermal
delivery of levonorgestrel (LNG) and ethinyl estradiol (EE), under normal conditions and
external conditions of heat, humidity, cold water and exercise.
delivery of levonorgestrel (LNG) and ethinyl estradiol (EE), under normal conditions and
external conditions of heat, humidity, cold water and exercise.
Normal conditions - average daily living activities, Dry Sauna - 10 minutes at 168.8 - 179.6
degrees Fahrenheit, Whirlpool - 10 minutes at 102.2 - 105.8 degrees Fahrenheit, Treadmill -
20 - 30 minutes at 60-80% max heart rate, Cold Water - 5 - 15 minutes at 71.6 degrees
Fahrenheit.
There will be three treatment periods. Subjects will be randomly assigned to one of the five
conditions for the treatment period. The subject will be exposed daily to the condition
assigned while wearing the patch. The study patch will be worn for a 7 day treatment period,
followed by a 7 day washout period. The total duration of the study is 6 weeks.
degrees Fahrenheit, Whirlpool - 10 minutes at 102.2 - 105.8 degrees Fahrenheit, Treadmill -
20 - 30 minutes at 60-80% max heart rate, Cold Water - 5 - 15 minutes at 71.6 degrees
Fahrenheit.
There will be three treatment periods. Subjects will be randomly assigned to one of the five
conditions for the treatment period. The subject will be exposed daily to the condition
assigned while wearing the patch. The study patch will be worn for a 7 day treatment period,
followed by a 7 day washout period. The total duration of the study is 6 weeks.
Inclusion Criteria:
- Healthy women, ages 18-45
- Body mass index (BMI)of ≥18 and less than or equal to 32, and weight ≥ 110 lbs.
- Willing to use a non-hormonal method of contraception if of childbearing potential, or
have already undergone previous bilateral tubal ligation or hysterectomy
- Willing to refrain from use of alcohol and grapefruit juice from 48 hours prior to
patch application until completion of each treatment period
- Willing to give informed consent to participate in study
Exclusion Criteria:
- Known or suspected pregnancy
- Breast-feeding or within 1 month after stopping breast-feeding
- Smokers
- Any disease that may worsen with hormonal treatment
- Hypersensitivity to transdermal preparations or sensitivity to surgical/medical tape
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