Study of the Effect of ITCA 650 on the PK/PD of Oral Contraceptive in Healthy Female Subjects

Completed · Phase 1 · Has a placebo group

Conditions studied: Healthy Adult Premenopausal Female Volunteers

In brief

A Phase 1, randomized, double-blind, placebo-controlled, crossover study to assess the effect of ITCA 650 on the pharmacokinetics (PK) of once daily administration of Levora® (ethinyl estradiol 0.3 mg (EE) and levonorgestrel 0.15 mg (LNG) in healthy premenopausal female subjects.

Key facts

Study ID

NCT02641990

Run by

Intarcia Therapeutics

People needed

28

Starts

2015-12-01

Expected to finish

2016-02-01

Last updated by the study team

2016-03-22

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women of childbearing potential.
• Use of a combination oral contraceptive ≥3 months immediately prior to screening.
• Willing to use an additional adequate method of contraception during the study and until 1 additional menstrual cycle following the end-of-study (EOS) visit. Adequate methods of contraception for women of child bearing potential (WOCBP) include: mechanical products (ie, intrauterine device [IUD]-copper IUD); or barrier methods (eg, diaphragm, condoms, cervical cap) with spermicide.
• Body mass index (BMI) ≥19 and ≤32 kg per meter squared.
• Weight ≥50 and ≤100 kg.
• Non-smoker or ex-smoker for >6 months prior to screening (and has stopped using other nicotine products ≥2 weeks prior to screening).

You may not qualify if…

• History of type 1 or type 2 diabetes.
• Received implanted contraceptives within 6 months prior to screening or injected contraceptives within 12 months prior to screening.
• History or evidence, within the last 6 months prior to the Screening Visit, of myocardial infarction, coronary revascularization (coronary artery bypass grafting or percutaneous coronary intervention), unstable angina, or cerebrovascular accident or stroke.
• History of uncontrolled hypertension.
• History or evidence of acute or chronic pancreatitis.
• History of liver disease.
• History of medullary thyroid cancer or a personal or family history of multiple endocrine neoplasia type 2.
• Poor thyroid, liver, or renal function.
• Weight loss surgery or requires weight loss medications.
• History of malignancy (not including basal or squamous cell carcinoma of the skin with past 5 years). (Subjects who have been disease free for 5 years may be included.)
• Estrogen-dependent growths; undiagnosed vaginal bleeding.
• History of active alcohol or substance abuse.
• Regular daily consumption of more than 12 g of alcohol in any form.
• Excessive in xanthine consumption (more than 5 cups of coffee or equivalent per day).
• Treatment with medications that affect GI motility.
• Any condition that would affect drug transit time or absorption (eg, gastrointestinal bypass surgery, partial or total gastrectomy, small bowel resection, chronic diarrhea, vagotomy, chronic gastroesophageal reflux disease, malabsorption, colostomy, Crohn's disease, ulcerative colitis, or celiac sprue).
• History of hypersensitivity to exenatide.
• Contraindications or warnings according to the specific label(s) for EE and/or LNG therapy.
• Women that are pregnant, lactating, or planning to become pregnant.
• Any use of anticoagulants with the exception of those given in prophylaxis prior to surgical intervention.
• History of or positive results on screening tests for hepatitis B and/or hepatitis C and/or human immunodeficiency virus (HIV).
• Recent surgery or planned in-patient surgery, dental procedure, or hospitalization during the study.
• History of migraine if aged >35 years or has focal symptoms associated with migraine.
• History of thrombophlebitis, thromboembolic disorders, or deep vein thrombophlebitis.
• Fasting triglycerides above upper limit of normal at Screening.

Where it is running

• QPS/Miami Research Associates — Miami, Florida, United States
• Compass Research — Orlando, Florida, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.