A Clinical Study in Healthy Women Which Aims to Explore the Intestinal Uptake of Two Different Tablets of GRTA9906 Into the Body and the Effect of Food on it

Inclusion Criteria

• •Female Caucasian volunteers aged 18 - 55 years.
• •Body mass index between 18 and 29 kilograms per square meter inclusive.
• •Good physical and mental health status (no current acute illness) determined on the basis of the medical history and a general clinical examination.
• •Normal supine blood pressure (systolic blood pressure greater than or equal to 90 Millimeter mercury (mmHg) and less than or equal to 145 mmHg, diastolic blood pressure greater than or equal to 45mmHg and less than or equal to 90 mmHg) and pulse (greater than or equal to 45 and less than or equal to 90 beats per minute).
• •Electrocardiogram (12 lead) considered as normal by the Investigator.
• •Results of laboratory tests within the normal ranges for the testing laboratory. The Investigator may include a participant having values outside the accepted range if, in his/her opinion, these values are of no clinical relevance. The decision will be justified.
• •Participants giving written consent to participate in this trial.
• •Negative pregnancy test (females of childbearing potential only).
• •Adequate contraception (females of childbearing potential only; adequate contraception is defined as any form of hormonal contraception or intra-uterine device that needs to be in place for a period of at least 2 months prior to screening. Additional barrier contraception must be used for the duration of the study, defined as from the time of screening to the post-study medical examination, and for at least one full month thereafter. A single barrier method alone or abstinence alone is not acceptable. Women of non-childbearing potential may be included if surgically sterile or post-menopausal for at least 2 years).
• •Must be able to tolerate high-fat and high-calorie study-meal.