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Assessment of Pharmacokinetics and Bioavailability of Carbon-14 ([14C])-Labelled Oxytocin | Clinical Trials | Clareo Health

WITHDRAWNPHASE1

Assessment of Pharmacokinetics and Bioavailability of Carbon-14 ([14C])-Labelled Oxytocin

NCT02911480•Oxytone Bioscience BV

View on ClinicalTrials.gov

Summary

The current study is designed as a phase I multiple dose study to evaluate the pharmacokinetics and bioavailability of \[14C\]-labelled oxytocin in healthy women.

Eligibility

Age

18 - 45 years

Sex

FEMALE

Healthy Volunteers

Yes

Inclusion Criteria

•Non-smoking women of child bearing potential (WOCBP)
•Body mass index (BMI) between ≥ 18.0 and ≤ 30.0 kg/m2
•Subject must voluntarily sign a written informed consent agreement approved by the Independent Ethics Committee (IEC) after explanation of the nature and objectives of the study and before any study specific procedure
•Subject must be in good physical and mental health as judged by the Investigator based on evaluation of medical and gynecological history, physical examination, clinical laboratory, ECG, and vital signs data
•Subject is willing and able to comply with all conditions and requirements of the study

Exclusion Criteria

•Lactation and/or pregnancy in the previous 6 months before screening, whichever is applicable
•Intention to become pregnant during the study or within 1 months after the follow up visit
•History of, or existing thromboembolic, cardiovascular or cerebrovascular disorder
•Treatment for any major psychiatric disorder in the previous 12 months or use of antidepressant medication before screening
•Any clinically significant abnormality following review of medical history, laboratory results and physical examination at screening as judged by the Investigator
•Conditions or disorders that might affect the absorption, distribution, metabolism or excretion of the study drugs
•Contraindications for the use of oxytocin
•Hypersensitivity to the active substances or to any of the excipients of the investigational product or reference therapy
•Present use or use within 30 days before the start of the study medication of one or more of the following medications: antihypertensive drugs, anti-coagulant therapy, medication that could affect myometrial contractility, sex steroids, prostaglandins and its analogues, inhalation anesthetics, vasoconstrictors/sympathomimetics and caudal anesthetics, vasopressin-like drugs
•Use of any prescribed or over-the-counter medication within 14 days before Day 1
+4 more criteria

Key Dates

Start Date

April 1, 2016

Primary Completion Date

February 1, 2017

Completion Date

August 31, 2017

Last Updated

April 6, 2018

Conditions

Healthy Women of Child Bearing Potential

Interventions

Oxytocin

DRUG