Safety and Pharmacokinetics Study of Linzagolix in Female Subjects With Normal and Impaired Hepat… (NCT03962049) | Clinical Trial Compass
CompletedPhase 1
Safety and Pharmacokinetics Study of Linzagolix in Female Subjects With Normal and Impaired Hepatic Function
United States24 participantsStarted 2019-05-15
Plain-language summary
The primary objective of this study is to assess the pharmacokinetics (PK) of linzagolix in subjects with varying degrees of impaired hepatic function compared to match control subjects with normal hepatic function
Who can participate
Age range18 Years – 75 Years
SexFEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Adult female, 18-75 years of age, inclusive, at screening
✓. Has a BMI ≥ 18.0 and ≤ 42.0 kg/m\^2 and weight ≥ 40 kg, at screening
✓. Aside from HI, be sufficiently healthy for study participation based upon medical history, physical examination, vital signs, electrocardiograms (ECGs), and screening clinical laboratory profiles, as deemed by the Principal Investigator (PI) or designee
✓. Has a score on the Child-Pugh scale at screening as follows:
✓. Has a diagnosis of chronic (\> 6 months), stable (no acute episodes of illness within the previous 2 months due to deterioration in hepatic function) hepatic insufficiency with features of cirrhosis due to any etiology
✓. Healthy adult female will be matched based upon age and BMI
✓. Medically healthy with no clinically significant medical history, physical examination, laboratory profiles, vital signs or ECGs, as deemed by the PI or designee.
Exclusion criteria
✕. Has a clinically active Grade 3 or 4 encephalopathy
✕. Has fluctuating or rapidly deteriorating hepatic function within the screening period, and up to 30 days prior to Day 1, in the opinion of the PI and Sponsor
✕. Has history of liver or other solid organ transplant
✕. Had any major surgery within 4 weeks prior to dosing
What they're measuring
1
Plasma pharmacokinetic (PK) parameter Cmax of linzagolix and of KP017
✕. Has a surgical (e.g., hepatectomy, nephrectomy, digestive organ resection) or medical condition other than HI which might significantly alter the absorption, distribution, metabolism, or excretion of linzagolix and its metabolites, or which may jeopardize the subject's safety in case of participation in the study in the opinion of the PI or designee
✕. Has any clinically significant illness, as judged by the PI or designee, within 4 weeks prior to dosing
✕. Has laboratory values at screening or check-in which are deemed to be clinically significant (especially derangement within liver function test), unless agreed in advance by the PI and the Sponsor