The purpose of this study is to assess the amount of LY3537031 that reaches the bloodstream and the time it takes for the body to get rid of it when given to participants with renal (kidney) impairment and to healthy participants.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
31
Administered SC
Omega Research Orlando LLC
Orlando, Florida, United States
Orlando Clinical Research Center
Orlando, Florida, United States
Indiana University School of Medicine
Indianapolis, Indiana, United States
New Zealand Clinical Research Christchurch
Christchurch, New Zealand
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY3537031
PK: AUC of LY3537031
Time frame: Predose on day 1 up to week 8 post dose
PK: Maximum Concentration (Cmax) of LY3537031
PK: Cmax of LY3537031
Time frame: Predose on day 1 up to week 8 post dose
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.