M0001 Effects on Oral Contraceptive Plasma Levels

Healthy Volunteers Clinical Trial

Official title:

The Effect of Prucalopride on the Plasma Levels of Oral Contraceptives (Ethinylestradiol and Norethisterone) in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01036893
• Other study ID #: M0001-C101
• Status: Completed
• Phase: Phase 1
• First received: December 18, 2009
• Last updated: May 16, 2011
• Start date: December 2009
• Est. completion date: May 2010

Study information

• Verified date: June 2010
• Source: Movetis
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Federal Institute for Drugs and Medical Devices
• Study type: Interventional

Clinical Trial Summary

This is a randomized, open-label, two-way cross-over drug-drug interaction Phase I trial.

The objectives of this phase I trial are to investigate in healthy female subjects:

• the effect of prucalopride on the absorption of ethinylestradiol and norethisterone acetate, the active constituents of several oral contraceptives, after the first dose of prucalopride.

• the effect of multiple oral dosing of 2 mg prucalopride, for 6 days o.d. (steady state), on the pharmacokinetics of ethinylestradiol and norethisterone acetate.

This trial will be conducted in healthy females of child bearing potential, i.e. females aged between 18 and 45 years (pre-menopausal).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: May 2010
• Est. primary completion date: February 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion criteria

Subjects who meet all of the following criteria are eligible for this trial:

1. Healthy females, aged between 18 and 45 years extremes included, who have regular menstrual cycle of 28 ± 3 days for the last 6 months.

2. Adequate use of non-hormonal birth control (double-barrier method (e.g. condom and spermicide, cervical cap and spermicide) or sterilization or vasectomy of the partner or certified abstinence).

3. Subjects are not smoking for at least 6 months prior to selection.

4. A body mass index (BMI) between 18 and 27 kg/m2, extremes included.

5. The subject is in good health based on a pre-trial physical and gynaecological examination, medical history, anamnesis, electrocardiogram (ECG) and the results of biochemistry, coagulation or haematology tests or a urinalysis carried out within 4 weeks before the start of the trial. If the results of the biochemistry, coagulation or haematology tests or the urinalysis are not within the laboratory's reference ranges the subject will be included only on condition that the investigator judges that the deviations are not clinically significant.

6. Subjects voluntarily signed written Informed Consent Form (ICF) in accordance with the regional laws or regulations, prior to the first trial related activity, indicating an understanding of the purpose of this trial.

7. Subjects are willing to adhere to the treatment regimen and trial procedures described in this protocol.

Exclusion criteria

Subjects meeting any of the following criteria will be excluded from the trial:

1. History, evidence or suspicion of alcohol or drug abuse (screening and Day -1).

2. History or evidence of cardiac arrhythmias, bronchospastic or cardiovascular disease (e.g. ischemic heart disease or cerebrovascular accident), hepatic or gastrointestinal, renal or endocrine (diabetes mellitus, thyrotoxicosis), or neurological (Parkinsonism) or psychiatric, gynaecological or dermatological disease, drug allergy.

3. Clinical significant abnormal ECG-intervals of morphology of the ECG, QT >500 ms or QTcB>470 ms.

4. Use of concomitant medication or oral contraceptives within 6 weeks prior to screening, or any hormonal depot-device within 6 months prior to screening . All medication, with the exception of paracetamol should be stopped.

5. Participation in an investigational drug trial in 30 days prior to the first visit.

6. Donation of blood in the 60 days preceding the first visit.

7. Pregnancy (as confirmed by a HCG test during screening and at Day 1 of each treatment session before dosing) or breast feeding.

8. Subjects with positive results for HIV, hepatitis B or C at screening.

9. Known allergy to the trial drugs ingredients/excipients.

10. Subject has contraindications for the use of oral contraceptives (known or suspected active venous thrombo-embolic disorder, known or suspected hormone dependent malignancies, undiagnosed vaginal bleeding, coagulation disorders, menstrual cycle depending migraine, lipid metabolism disorders, hepatic disorders)

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Healthy Volunteers

Intervention

Drug:
• prucalopride
prucalopride 2 mg oral dosing o.d. for 6 days

Locations

Country	Name	City	State
Germany	FOCUS GmbH	Neuss

Sponsors (2)

Lead Sponsor	Collaborator
Movetis	FOCUS GmbH

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	plasma levels oral contraceptives		first days	No
Primary	Plasma levels oral contraceptives after steady state		5 days	No