| Eligibility |
Inclusion Criteria:
- Non-smoker or past-smoker (an ex-smoker is defined as someone who has completely
stopped using nicotine products, including nicotine cessation therapy, for at least
180 days prior to the first study drug administration).
- Body Mass Index (BMI) =18.5 and = 30 kg/m2, inclusive and body weight between 45 kg
and 100 kg(on the day of screening).
- Subject is available for the whole study and has provided her written informed consent
- Subjects in good health, as determined by screening medical history, physical
examination, vital signs assessments (pulse rate, systolic and diastolic blood
pressure, and body temperature) and 12-lead electrocardiogram (ECG) . Minor deviations
outside the reference ranges will be acceptable, if deemed not clinically significant
by the Investigator.
- Acceptance of use of contraceptive measures during the whole study.
- Normal Liver and kidney function tests (on Screening)
- All laboratory screening results within the normal range, or deemed clinically
insignificant by Investigator.
- The thickness of the endothelial layer according to ultrasound of the pelvic organs is
not less than 2 mm and not more than 4 mm (on Screening)
Exclusion Criteria:
- Known cardiovascular disease, history of hypotension
- History of gout, urolithiasis, nephrolithiasis and hyperuricaemia
- Gastrointestinal diseases, including gastric ulcer, renal or hepatic diseases and/or
pathological findings present or in history, which might interfere with the drug
pharmacokinetics.
- Known history or presence of food allergies, or any condition known to interfere with
the absorption, distribution, metabolism or excretion of drugs.
- Acute or chronic diseases and/or clinical finding which may interfere with the aims of
the study or with the drug's safety, tolerability, bioavailability and/or
pharmacokinetics of the Investigational Medicinal Product (IMP).
- History of severe allergy or allergic reactions to the study IMP, its excipients or
related drugs, wheat allergy history.
- Positive result of urine pregnancy test at screening or breast-feeding or lack of
results of pregnancy test.
- Postponed acute diseases of the female genitals during the last 3 months, including
vaginitis and / or vulvovaginitis.
- Chronic inflammatory and/or atrophic diseases of the pelvic organs.
- Benign neoplasms and anamnesis of hyperplastic processes, including mastopathy and
endometrial hyperplasia.
- Surgical intervention on the pelvic organs, including hysterectomy, adnexectomy (It
doesn't include the Subject who had a previous history of Cesarean section for 5 years
or more provided that the Cesarean section was not for pathological reasons and/ or
accompanied with cervix and uterus diseases or external genitals organs disease).
- Arterial or venous thromboembolism or thrombophlebitis in anamnesis.
- Reporting drug of abuse at screening
- Positive result of alcohol breath test at screening.
- The presence of nicotine or cotinine in urine at the screening.
- Serious mental disease and/or inability to cooperate with clinical team.
- Sitting blood pressure after a minimum of 5 minutes of rest is out of the range of
90-140 mmHg for systolic BP and/or 60-90 mmHg for diastolic BP and/or heart rate out
of the range of 50-100 bpm during the screening procedure.
- Body temperature is out of the range of 35.7-37.6° C at screening.
- Orthostatic hypotension during the screening procedure or in the history.
- Reporting Drug, alcohol (of = 40 g per day pure ethanol), solvents or caffeine abuse
at screening.
- Getting a tattoo, body piercing or any cosmetic treatment involving skin piercing
within 90 days before the screening unless evaluated by Investigator as
non-significant for inclusion in the study.
- Donation of at least 400 ml of blood within 60 days, or more than 150 ml of blood
within 30 days, or more than 100 ml blood plasma or platelets within 14 days before
study Period I.
- Following a special diet (e.g. vegetarian) or dieting one month before the study
initiation
- Allergy on peanut in anamnesis
- Less than 80 days between exit procedure in previous study and the first dosing in
this study.
- Any significant clinical abnormality including Hepatitis B surface antigen (HBsAg),
hepatitis C virus (HCV), and / or (human immunodeficiency virus) HIV. (On screening)
- Abnormal Kidney and/or Liver function tests and being assessed as clinically
significant by the attending physician. (On screening).
- Results of laboratory tests are outside the normal range and being assessed as
clinically significant by the attending physician (On screening).
- Previous liver disease or elevations in serum transaminases alanine aminotransferase
(ALT) or aspartate aminotransferase AST =1.0 upper limit of normal (ULN) at the
screening (ALT for women up to 63 U/L and AST up to 37 U/L).
- Any significant clinical abnormality, including a positive result of HBsAg and/or HCV
and/or HIV test during screening procedure.
- Uric acid level for women > 6.0 mg/dl at the screening
- History of kidney disease with impaired renal function and level of creatinine in
blood out of the normal laboratory range based on screening
- Anemia, hemoglobin below 12.0 g/L at screening.
- The intake of caffeine, xanthenes, or carbon dioxide (CO2)-containing beverages within
18 hours of drug administration
- Consumption of alcohol, grapefruit or grapefruit containing products within 7 days of
drug administration.
- Ingestion of any supplements like vitamins or herbal products within 7 days prior to
the initial dose of the study medication.
- Exhausting physical exercise in the last 48 hours (e.g. weight lifting) or any recent
significant change in dietary or exercise habits.
- Abnormal Vital Signs and being assessed as clinically significant by the attending
physician.
- Vomiting, Diarrhea on admission.
- Use of organ-toxic drugs or systemic drugs known to substantially alter liver
metabolism within 90 days before the first dosing.
- Use of any prescription medication for a period of 14 days before the first dosing.
- Any systemic over-the-counter (OTC) drug treatment and/or vitamins and/or herbal
treatment and/or food supplements within 14 days before the first dosing.
- Clinically significant illness within 28 days before the first dosing, including major
surgery.
- Positive results of drug of abuse at check-in.
- Positive result of alcohol breath test at check-in.
- Reporting Drug, alcohol (of = 40 g per day pure ethanol), solvents or caffeine abuse
at check-in
- Positive urine pregnancy test at check-in.
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