The purpose of this study is to learn what happens to nemtabrutinib in a person's body when given to participants with severe kidney disease and to healthy participants.
Eligibility
Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria:
The main inclusion criteria include but are not limited to the following:
All participants:
* Has a body mass index (BMI) ≥18.0 and ≤40.0 kg/m\^2
Participants with Severe Renal impairment (RI):
* The participant has stable renal function as determined by historical measurements.
Healthy volunteers:
* Is medically healthy with no clinically significant medical history
Exclusion Criteria:
The main exclusion criteria include but are not limited to the following:
Renal Impairment Participants:
* History of any illness, other than renal impairment, that, in the opinion of the investigator, might confound the results of the study or poses an additional risk to the participant by their participation in the study.
Healthy Matched Control Participants:
* History of clinically significant endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological (including stroke and chronic seizures) abnormalities or diseases. Participants with a remote history of uncomplicated medical events (eg, uncomplicated kidney stones, as defined as spontaneous passage and no recurrence in the last 5 years, or childhood asthma) may be enrolled in the study at the discretion of the investigator
Primary outcome measure(s)
Area Under the Concentration Time Curve From Time 0 Extrapolated to Infinity (AUC0-inf) of Nemtabrutinib in Plasma — At designated timepoints up to approximately 336 hours postdose Blood samples will be collected to determine the AUC0-inf of Nemtabrutinib in plasma.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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