- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00163033
Study to Evaluate 3 Dosages of Estetrol After 28 Days Administration in Healthy Postmenopausal Women
Phase I Study to Evaluate the Safety, Tolerability, PK and Pharmacodynamics of 3 Dosages of Estetrol, the Lowest Dose of 2 mg Estetrol Compared With 2 mg of E2, After Daily Oral Administration for 28 Days in Healthy Postmenopausal Women
Study Overview
Detailed Description
This is a partly randomized open-label study in healthy postmenopausal women. Groups are treated in the following sequence: first a 2 mg estetrol group together with a 2 mg estradiol group. When the dose of 2 mg estetrol is safe and the tolerability is good, a next higher dose group of estetrol will start, possibly followed by two next higher dose groups if the previous dose group is safe and the tolerability is good.
The primary objective of this study is to investigate the safety and tolerability of estetrol during multiple dosing for 28 days. Furthermore steady state pharmacokinetics and some pharmacodynamic parameters of estetrol will be investigated. In addition, the pharmacokinetics and pharmacodynamic effects of the 2 mg estetrol group will be compared with those of the 2 mg estradiol group.
In each group 5 postmenopausal women will be included with > 50 hot flushes per week and 5 postmenopausal women with < 10 hot flushes per week. These criteria are set to get a more homologous composition in each group.
Study Type
Enrollment (Actual)
Phase
- Phase 1
Contacts and Locations
Study Locations
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Utrecht, Netherlands, 3584 CJ
- Kendle Clinical Pharmacology Unit
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Postmenopausal women not older than 70 years of age at the time of screening (menopause defined as ≥ 6 months amenorrhea with serum follicle-stimulating hormone [FSH] levels ≥ 40 IU/L and serum E2 < 73 pmol/L).
- Body mass index 18-30 kg/m2 inclusive.
- Good physical and mental health, as judged by the Investigator, determined by medical history, physical examination, clinical laboratory values, vital signs, and electrocardiogram (ECG) recording.
- Willing to give written informed consent.
- Either > 50 hot flushes per week or < 10 hot flushes per week
Exclusion Criteria:
- Clinically significant abnormal results of routine hematology, serum biochemistry, urinalysis, and/or ECG in the opinion of the Investigator at screening.
- Clinically significant abnormal mammogram (presence of any non-cystic mass) within one year before study start.
- Clinically significant abnormalities of the uterus and/or ovaries detected by examination and/or ultrasound (non-physiological ovarian mass or significant uterine pathology or an endometrium greater than 6 mm).
- A cervical smear with clinically relevant abnormal cytology within one year before study start.
Previous use of estrogen/progestogen within:
- 6 months for depot preparations.
- 8 weeks for oral preparations or progestogen containing intrauterine device (IUD).
- 4 weeks for transdermal preparations.
- Use of hormone containing implant at any time.
Contraindications for using steroids:
- A history of, or existing thromboembolic, cardiovascular, or cerebrovascular disorder.
- A history of, or existing conditions predisposing to, or being prodrome of, a thrombosis.
- A known defect in the blood coagulation system (e.g. deficiencies in antithrombin-III [AT-III], protein C, S, and activated protein C [APC] resistance).
- A medical history positive for the presence of more than one risk factor for vascular disease (e.g. dyslipoproteinemia; diabetes mellitus; hyperhomocysteinemia; systemic lupus erythematosus; chronic inflammatory bowel disease; smoking; venous thromboembolism in sibling or parent below the age of 50, or arterial disease in sibling or parent below the age of 30-35).
- Hypertension, i.e. systolic blood pressure >160 mm Hg and/or diastolic blood pressure >100 mm Hg.
- Disturbance of liver function: cholestatic jaundice, a history of jaundice in pregnancy or jaundice due to previous estrogen use, Rotor syndrome and Dubin-Johnson syndrome.
- Known or suspected estrogen-dependent tumors or endometrial hyperplasia
- Undiagnosed vaginal bleeding.
- Porphyria.
- A history during pregnancy or previous estrogen use of severe pruritus, herpes gestationis, or deterioration of otosclerosis.
- Any medication (including over-the-counter [OTC] products) from 14 days prior to the day of dosing except for occasional non-steroidal anti-inflammatory drugs (NSAID; e.g. ibuprofen); paracetamol is not permitted.
- Any enzyme affecting drugs from 30 days prior to Day 1 and the use of griseofulvin, primidone, oxcarbazepine, topiramate, felbamate, or herbal remedies containing hypericum perforatum (St. John's wort).
- Presence of significant allergies or other serious diseases.
- Smoking more than 10 cigarettes or equivalent per day.
- Administration of investigational drugs within 3 months before start of study medication.
- A history of (within 12 months) alcohol or drug abuse.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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safety of estetrol
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tolerability of estetrol
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Secondary Outcome Measures
Outcome Measure |
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steady state pharmacokinetics of estetrol
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pharmacodynamic effects of estetrol
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to compare the pharmacokinetics and pharmacodynamic effects of 2 mg estetrol with 2 mg estradiol
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to investigate the effect on the number of hot flushes and sweating of 2 mg estetrol compared with 2 mg estradiol
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Herjan Coelingh Bennink, MD, PhD, Pantarhei Bioscience
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PR3054
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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