A Study of the Blood Levels of Palovarotene in Participants With Abnormal Liver Function Compared to Healthy Adult Participants After Intake of a Single Dose

Launched by IPSEN · Apr 1, 2025

Keywords

ClinConnect Summary

This clinical trial is studying how a medication called palovarotene is processed by the body in people with different levels of liver function. The main goal is to see how moderate and severe liver impairment affects the way the body handles a single dose of 10 mg of this drug, compared to healthy adults with normal liver function. Participants will be grouped based on their liver health: one group will consist of healthy individuals, another group will include those with moderate liver impairment, and a third group will be added later for those with severe liver impairment if the first two groups show safe results.

To be eligible for the trial, participants must be between 18 and 70 years old and have a stable liver condition for at least three months. They should also weigh at least 60 kg and have a body mass index within a specific range. Throughout the trial, participants will stay in a clinical unit for five days for safety checks and blood tests, where researchers will look at how the drug interacts with the body. After this period, they'll return for a final visit on Day 10. This study is currently recruiting participants and aims to gather important safety information about palovarotene.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Male and female participants must be 18 to 70 years of age (inclusive) at the time of signing informed consent.
• • Body weight at least 60.0 kg with body mass index (BMI) within the range of 18.0 and 36.0 kg/m² (inclusive), at screening. BMI of \>36.0 to ≤37.0 may be eligible if participant has ascites scoring 3 points on the C-P criteria.
• • Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical trials
• • Clinical diagnosis of chronic hepatic disease (stable for more than 3 months) with a documented history of underlying hepatic insufficiency and no acute episodes of illness within 30 days prior to Day -1 (admission) and no significant change in disease status (i.e. up to 1 point in the C-P classification) from screening to Day -1.
• • A stable medication regimen, defined as not starting new therapy(ies) or significant changing dosage(s) within 30 days prior to dosing.
• Exclusion Criteria:
• • Presence or significant history of cardiovascular, respiratory, hepatic (except for the hepatic impairment for those concerned), renal, gastrointestinal, biliary, mucocutaneous, endocrinological, haematological or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs, constituting a risk when taking the study intervention, or interfering with the interpretation of data.
• • Lymphoma, leukaemia or any malignancy within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for 3 years.
• • Breast cancer within the past 10 years.
• • Use of any medications (prescription or over the counter), herbal tea, energy drinks (including natural stimulants), herbal products (e.g. St. John's wort, garlic, milk thistle) or supplements/supratherapeutic doses of vitamins within 14 days prior to Day 1 and through discharge, apart from those approved by the investigator and the sponsor's medical monitor. Those with hepatic impairment may take concomitant medications
• • Use of any medications that are moderate or strong inhibitors or inducers of CYP3A4
• • Donation or loss (excluding volume drawn at screening or during menses) of more than 250 mL of blood or blood product within 3 months prior to screening. In addition, plan of blood donation within 8 weeks after the last PK sampling.
• • Presence of hepatitis B surface antigen (HBsAg) at screening or within 3 months prior to the dose of study intervention.
• • Positive hepatitis C antibody test result at screening or within 3 months prior to the dose of study intervention. Note: Participants with positive hepatitis C antibody due to prior resolved disease can be enrolled if a confirmatory negative hepatitis C ribonucleic acid (RNA) test is obtained.
• • Positive hepatitis C RNA test result at screening or within 3 months prior to the dose of study intervention. Note: Test is optional and participants with negative hepatitis C antibody test are not required to also undergo hepatitis C RNA testing.
• • Sensitivity to the study intervention, or components thereof (including inactive ingredients), or drug or other allergy that, in the opinion of the investigator (or medical monitor), contraindicates participation in the study
• • Evidence of relevant active disease at screening, including gastroenterological (other than hepatic cirrhosis), cardiac (e.g. myocardial infarction in the past year, angina or congestive heart failure), renal, respiratory, haematological, neuropsychiatric or neoplastic (basal or squamous cell skin cancer is acceptable) disease.
• • Acute hepatitis B (positive for HBsAg) or acute hepatitis C (positive for anti-hepatitis C virus (HCV) for a duration of less than 6 months). Note: Participants with chronic HCV (positive for HCV RNA or anti-HCV for more than 6 months) are eligible for enrolment, if stable, as assessed by the investigator.
• • Primary sclerosing cholangitis or preliminary diagnosed biliary obstruction at screening.
• • Current or chronic history of liver disease. This includes (but is not limited to hepatitis virus infections), drug- or alcohol-related liver disease, non-alcoholic steatohepatitis, autoimmune hepatitis, hemochromatosis, Wilson's disease, α-1 antitrypsin deficiency, primary biliary cholangitis, primary sclerosing cholangitis, or any other liver disease considered clinically significant by the investigator.