Clinical Drug Experience Knowledgebase

Criteria

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.