Hepatic Function Abnormal
Conditions
Brief summary
This is a Phase 1, parallel, open-label, 3-arm study to investigate the pharmacokinetic (PK) parameters of amcenestrant in female participants aged 40 to 75 years with mild and moderate hepatic impairment, and in matched participants with normal hepatic function.
Detailed description
The total study duration from screening period is approximately 41 days.
Interventions
DRUGamcenestrant
tablet for oral use
Sponsors
Sanofi
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
40 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
For participants with hepatic impairment: * Participant must be 40 to 75 years of age, inclusive. * Female participants who are postmenopausal or are post-bilateral surgical oophorectomy not linked to a history of cancer. Menopause is defined as being amenorrheic for at least 12 months without an alternative medical cause, with plasma FSH level \>30 IU/L or age ≥60 years. * Stable chronic liver disease assessed by medical history, physical examination, laboratory values * Body weight within the range 50 kg (40 kg for site in South Korea) to 110 kg and body mass index (BMI) within the range 18 to 36 kg/m2, inclusive. * For moderate hepatic impairment cohort: Child-Pugh total score ranging from 7 to 9, inclusive. * For mild hepatic impairment cohort: Child-Pugh total score ranging from 5 to 6, inclusive For matched subjects: * Participant must be 40 to 75 years of age, inclusive. * Female participants who are postmenopausal or are post-bilateral surgical oophorectomy not linked to a history of cancer. Menopause is defined as being amenorrheic for at least 12 months without an alternative medical cause, with plasma FSH level \>30 IU/L or age ≥60 years. * Certified as healthy by a comprehensive clinical assessment (detailed medical history and complete physical examination). * Body weight within the range 50 kg (40 kg for site in South Korea) to 100 kg and body mass index (BMI) within the range 18 to 36 kg/m2, inclusive.
Exclusion criteria
For participants with hepatic impairment: * History or presence of drug or alcohol abuse (alcohol consumption more than 40 g per day on a regular basis) within 1 year before inclusion. * Smoking regularly more than 15 cigarettes or equivalent per day, unable to refrain from smoking over 8 cigarettes per day during the institutionalization (Smoking is not allowed within 8 hours after amcenestrant administration). * Excessive consumption of beverages containing xanthine bases (more than 5 cups or glasses per day). * Non-live vaccines including Covid-19: last administration of a vaccine within 1 week (symptoms-free) to 2 weeks before inclusion. * Any consumption of citrus fruits (grapefruit, orange, etc) or their juices within 72 hours before inclusion. * Use of any herbal medicines 1 week before IMP administration and up to the end of PK sampling following the IMP administration * Live-vaccines: last administration of a vaccine within 4 weeks before inclusion * Treatment with a strong CYP3A, CYP2C8 or any UGTs inhibitor within 14 days before first study treatment administration or 5 half-lives whichever is longer. * Treatment with a strong or moderate CYP3A, CYP2C8 or any UGTs inducer within 14 days before first study treatment administration or 5 half-lives whichever is longer. * Uncontrolled clinically relevant cardiovascular, pulmonary, gastrointestinal, metabolic, hematological, neurological, psychiatric, systemic, ocular, gynecologic, renal, infectious disease, severe hepatic impairment (Child-Pugh total score greater than or equal to 10), or signs of acute illness, hepatocarcinoma, acute hepatitis, Hepatic encephalopathy Grade 2, 3, and 4 * Esophageal bleeding, which is caused by esophageal varices, within 3 months before inclusion For matched subjects: * History or presence of drug or alcohol abuse (alcohol consumption more than 40 g per day on a regular basis) within 1 year before inclusion. * Smoking regularly more than 15 cigarettes or equivalent per day, unable to refrain from smoking over 8 cigarettes per day during the institutionalization (Smoking is not allowed within 8 hours after amcenestrant administration). * Excessive consumption of beverages containing xanthine bases (more than 5 cups or glasses per day). * Any history or presence of clinically relevant cardiovascular, pulmonary, gastrointestinal, hepatic, renal, metabolic, hematological, neurological, osteomuscular, articular, psychiatric, systemic, ocular, gynecologic, or infectious disease, or signs of acute illness, unless the Investigator considers an abnormality to be not clinically significant. * Frequent headaches and/or migraine, recurrent nausea and/or vomiting (for vomiting only: more than twice a month. * Non-live vaccines including Covid-19: last administration of a vaccine within 1 week (symptoms-free) to 2 weeks before inclusion * Live-vaccines: last administration of a vaccine within 4 weeks before inclusion * Treatment with a strong CYP3A, CYP2C8 or any UGTs inhibitor within 14 days before first study treatment administration or 5 half-lives whichever is longer. * Treatment with a strong or moderate CYP3A, CYP2C8 or any UGTs inducer within 14 days before first study treatment administration or 5 half-lives whichever is longer. * Any consumption of citrus fruits (grapefruit, orange, etc) or their juices within 72 hours before inclusion. * Use of any herbal medicines 1 week before IMP administration and up to the end of PK sampling following the IMP administration The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pharmacokinetic (PK) assessment: Maximum plasma concentration observed (Cmax) | From Day 1 to Day 5 | Maximum plasma concentration observed (Cmax) of amcenestrant |
| PK assessment: Area under the plasma concentration (AUC) | From Day 1 to Day 5 | Area under the plasma concentration versus time curve of amcenestrant |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| PK assessment: Tmax of amcenestrant | From Day 1 to Day 5 | Time to reach Cmax of amcenestrant |
| PK assessment: Area under the plasma concentration versus time curve (AUClast) of amcenestrant | From Day 1 to Day 5 | Area under the plasma concentration versus time curve calculated using the trapezoidal method from time zero to the real time tlast of amcenestrant |
| PK assessment: Maximum unbound plasma concentration (Cmax u) of amcenestrant | From Day 1 to Day 5 | Maximum unbound plasma concentration of amcenestrant |
| PK assessment: AUC of M7 | From Day 1 to Day 5 | Area under the plasma concentration versus time curve extrapolated to infinity of M7 |
| PK assessment: Cmax of M7 | From Day 1 to Day 5 | Maximum observed plasma concentration of M7 |
| PK assessment: AUClast of M7 | From Day 1 to Day 5 | Area under the plasma concentration versus time curve calculated using the trapezoidal method from time zero to the real time tlast of M7 |
| PK assessment: AUCu of amcenestrant | From Day 1 to Day 5 | Unbound area under the plasma concentration versus time curve extrapolated to infinity of amcenestrant |
| Number of participants with adverse events (AEs) / treatment-emergent adverse events (TEAEs) | From the date when the ICF is signed to the end of study (approximately Day 10) | Incidence of adverse events (AEs) and treatment-emergent adverse events (TEAEs) |
Countries
Germany, South Korea
Outcome results
None listed