Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Houston, Texas 77042


Purpose:

The purpose of this study was to evaluate the relative bioavailability of a test formulation of norethindrone/ethinyl estradiol 0.4 mg/0.035 mg chewable tablets (Teva Pharmaceuticals, USA) compared to the reference listed product, FEMCON® Fe (norethindrone/ethinyl estradiol and ferrous fumarate) 0.4 mg/0.035 mg Chewable tablets (Warner Chilcott) under fed conditions in healthy, non-tobacco using, adult female subjects.


Criteria:

Inclusion Criteria: - Females, 18-45 years of age inclusive with Body Mass Index within 18-30 kg/m2 inclusive, as described in Novum Standard Operating Procedures. Female subjects must either abstain from sexual intercourse or use a reliable non-hormonal method of contraception (e.g. condom with spermicide, diaphragm, non-hormonal IUD) from at least 14 days prior to the first study dosing, throughout the study, and until 14 days after the last dose. - Normal menstrual cycle. - Good health as determined by lack of clinically significant abnormalities in health assessments performed at screening. - Signed and dated informed consent form, which meets all criteria of current FDA regulations. Exclusion Criteria: - Post menopausal or have irregular menstrual cycle. - Pregnant, lactating, or likely to become pregnant during the study. - History of any drug hypersensitivity or intolerance which, in the opinion of the Investigator, would compromise the safety of the subject or the study. - Significant history or current evidence of chronic infectious disease, system disorder, or organ dysfunction. - Presence of gastrointestinal disease or history of malabsorption within the last year. - History of psychiatric disorders occurring within the last two years that required hospitalization or medication. - Presence of a medical condition requiring regular treatment with prescription drugs. - Use of pharmacologic agents known to significantly induce or inhibit drug-metabolizing enzymes within 30 days prior to dosing. - Participation in any clinical trial within 30 days prior to dosing. - Drug or alcohol addiction requiring treatment in the past 12 months. - Donation or significant loss of whole blood (480 mL or more) within 30 days or plasma within 14 days prior to dosing. - Positive test results for HIV, Hepatitis B surface antigen, or Hepatitis C antibody. - Positive test results for drugs of abuse at screening. - Positive serum pregnancy test. - Subjects who have ever had progestational hormone implants. - Subjects who have had progestational hormone depot injections within 12 months proceeding dosing. - Subjects who are using or have used within the 3 months preceding dosing any vaginally administered estrogen or progestin-containing products. - Any personal or strong family history of estrogen- or progestogen-dependent tumors. - History of clinically significant fibrocystic breast disease. - Subjects with a history of thromboembolic disorders, myocardial infarction, or stroke. - Use of norethindrone or ethinyl estrodiol-containing oral contraceptives within 30 days of initial dosing. - Hysterectomy or oophorectomy (unilateral or bilateral) - User of tobacco of nicotine containing products within 30 days of the start of the study.


NCT ID:

NCT01344369


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Houston, Texas 77042
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.