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A Study to Evaluate the Impact of Renal Impairment on the Pharmacokinetics (PK) of Ribupatide

StatusNot Yet Recruiting
PhasePhase 1
SponsorKailera
Started2026-09-08
View on ClinicalTrials.gov ↗
The primary objective of the study is to estimate the PK parameters of ribupatide in participants with severe renal impairment or end-stage kidney disease (ESKD) after a single dose of ribupatide subcutaneous (SC) injection compared with participants with normal renal function.
Trial Details
NCT Number NCT07793929
Lead Sponsor Kailera
Conditions End Stage Renal Disease, Renal Impairment, Obesity, Overweight
Enrollment 32 participants
Start Date 2026-09-08
Primary Completion 2028-02-08 (estimated)
Study Completion 2028-02-08 (estimated)
Updated on ClinicalTrials.gov 2026-09-03