A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Volenrelaxin in Adults With Chronic Kidney Disease
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Volenrelaxin in Adults With Chronic Kidney Disease
The main purpose of this study is to investigate the efficacy and safety of Volenrelaxin in adults with Chronic Kidney Disease. The study will last about 24 weeks.
Inclusion Criteria:
Exclusion Criteria:
Have any one of the following cardiovascular conditions 90 days prior to screening:
Have a documented New York Heart Association (NYHA) Class IV heart failure at the time of screening.
Have chronic or intermittent hemodialysis or peritoneal dialysis 90 days prior to screening.
Have acute dialysis or acute kidney injury 90 days prior to screening.
Have a history of a congenital or hereditary kidney disease, polycystic kidney disease, lupus nephritis, anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, and nephrotic syndrome
Requires chronic immunosuppression.
Have HbA1c >8.5% at screening
Have had a transplanted organ or are awaiting an organ transplant
Have a diagnosis or history of malignant disease within 5 years prior to baseline.
Have symptomatic hypotension.
Have acute or chronic hepatitis.
Hinsdale, Illinois 60521, United States
Huntley, Illinois 60142, United States
Fort Wayne, Indiana 46804, United States
Indianapolis, Indiana 46227, United States
Taian, Shandong 271000, China
Kamakura-shi, Kanagawa 247-0056, Japan