Status:
COMPLETED
A Study of Tirzepatide (LY3298176) in Participants With Impaired Kidney Function
Lead Sponsor:
Eli Lilly and Company
Conditions:
Renal Insufficiency
End Stage Renal Disease
Eligibility:
All Genders
18-85 years
Phase:
PHASE1
Brief Summary
The purpose of this study is to assess how fast tirzepatide gets into the blood stream and how long it takes the body to remove it in participants with impaired kidney function compared to healthy par...
Eligibility Criteria
Inclusion
- All Participants:
- Women not of childbearing potential may participate and include those who are infertile due to surgical sterilization (hysterectomy, bilateral oophorectomy, or tubal ligation), congenital anomaly such as mullerian agenesis; or postmenopausal
- Are between the body mass index (BMI) of 19.0 and 40.0 kilograms per meter squared (kg/m²), inclusive, at screening
- Healthy Participants:
- \-- Healthy males or females as determined by medical history, physical examination, and other screening procedures, with normal renal function, assessed by estimated glomerular filtration rate (eGFR) ≥90 milliliters per minute (mL/min) at screening
- Participants with Renal Impairment or ESRD:
- \-- Males or females with stable mild to severe renal impairment, assessed by eGFR or with ESRD (having received hemodialysis for at least 3 months)
- Participants with Type 2 Diabetes Mellitus (T2DM) and Renal Impairment or ESRD:
- Have T2DM controlled with diet or exercise alone or stable on metformin for at least 8 weeks
- Taking stable doses of over-the-counter or prescription medications (eg, antihypertensive agents, aspirin, lipid-lowering agents) for treatment of concurrent medical conditions are permitted to participate providing they have been stable on their treatment regimen for at least 4 weeks
- Have a hemoglobin A1c (HbA1c) ≥7.0% and ≤11.0% at screening
Exclusion
- All Participants:
- Women of childbearing potential
- Have known allergies to tirzepatide or related compounds
- Have a personal or family history of medullary thyroid carcinoma or have multiple endocrine neoplasia syndrome type 2
- Have serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) \>2× the upper limit of normal (ULN) or total bilirubin (TBL) \>1.5× ULN
- Have a history or presence of pancreatitis (history of chronic pancreatitis or idiopathic acute pancreatitis), elevation in serum amylase or lipase or GI disorder (eg, relevant esophageal reflux or gall bladder disease) or any GI disease which impacts gastric emptying (eg, gastric bypass surgery, pyloric stenosis, with the exception of appendectomy) or could be aggravated by glucagon-like peptide-1 (GLP-1) analogs or dipeptidyl peptidase IV (DPP-IV) inhibitors
- Participants with Renal Impairment or ESRD:
- Have hemoglobin \<8.5 grams per deciliter (g/dL) or significant active hematological disease from causes other than underlying renal disease.
- Have used any drug indicated for medical care of the participant's renal impairment, which is not established in dose and administered for at least 7 days before LY3298176 administration
- Participants with T2DM and Renal Impairment or ESRD:
- Have taken any glucose-lowering medications other than metformin, including insulin, in the past 3 months before screening
- Have had more than 1 episode of severe hypoglycemia, as defined by the American Diabetes Association criteria, within 6 months before entry into the study or has a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms
Key Trial Info
Start Date :
March 30 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 19 2019
Estimated Enrollment :
45 Patients enrolled
Trial Details
Trial ID
NCT03482024
Start Date
March 30 2018
End Date
August 19 2019
Last Update
March 23 2023
Active Locations (4)
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1
Orange County Research Center
Tustin, California, United States, 92780
2
Clinical Pharmacology of Miami
Miami, Florida, United States, 33014
3
Orlando Clinical Research Center
Orlando, Florida, United States, 32809
4
High Point Clinical Trials Center
High Point, North Carolina, United States, 27265