Overview

The Effect of BMS-986142 on the Pharmacokinetics of a Combined Oral Contraceptive (OC) Containing Ethinyl Estradiol (EE) and Norethindrone Acetate (NET) in Healthy Female Subjects

Status:
Completed
Trial end date:
2016-10-01
Target enrollment:
0
Participant gender:
Female
Summary
This is an open-label, 2-cycle, multiple-dose, single-sequence study in women of child-bearing potential. The primary objective is to assess the effect of BMS-986142 on the pharmacokinetics (PK) of Combined Oral Contraceptive Containing Ethinyl Estradiol and Norethindrone Acetate.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Bristol-Myers Squibb
Treatments:
Contraceptive Agents
Contraceptives, Oral
Contraceptives, Oral, Combined
Estradiol
Ethinyl Estradiol
Norethindrone
Norethindrone acetate
Norethindrone acetate, ethinyl estradiol, ferrous fumarate drug combination
Norinyl
Criteria
Inclusion Criteria:

- Signed Informed Consent

- Target population: Healthy females with no clinically significant deviations from
normal in medical history, physical examinations, vital signs, electrocardiograms
(ECGs), physical measurements, and clinical laboratory tests that are willing to
switch to Loestrin during the study.

- Body Mass Index (BMI) between 18 to 32 kg/m2.

- Women of childbearing potential with intact ovarian function and history of regular
menstrual cycles must have been on a stable regimen of combination of birth control
containing ethinyl estradiol without evidence of clinically significant breakthrough
bleeding or spotting for at least 2 consecutive months prior to Day -1.

- Women of childbearing potential must agree to follow instructions for method(s) of
contraception for the duration of treatment with study drugs (53 days) plus 5
half-lives of BMS-986142 (3 days) plus 30 days (duration of ovulatory cycle) for a
total of 86 days.

Exclusion Criteria:

- History of any chronic or acute illness including active TB in the last 3 years,
recent infection, gastrointestinal disease, smoking within less than 6 months prior to
dosing, alcohol abuse, inability to tolerate oral medication, or inability to be
venipunctured.

- History of jaundice or irregular bleeding associated with taking oral contraceptives,
frequent headaches, cerebrovascular or coronary-artery disease, retinal vascular
lesions, cancer of the breast or endometrium, deep venous thrombosis, pulmonary
embolism, stroke, transient ischemic attack, or phlebitis.

- Vaccination or plans for vaccination with any live vaccine 12 weeks prior to first
dose of study drug, during the course of the study, or 30 days after the last dose of
study drug.

- Evidence of organ dysfunction or any clinically significant deviation from normal in
physical examination, vital signs, electrocardiograms, or clinical laboratory
determinations beyond what is consistent with the target population.

- History of allergies and adverse drug reaction to any oral contraceptive compounds or
Bruton tyrosine kinase (BTK) inhibitors.