Inflammation Clinical Trial
Official title:
First-in-human Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of NOX-H94
This is the first clinical trial with NOX-H94. The purpose of this clinical trial is to identify a safe and efficacious treatment regimen for the clinical development of NOX-H94 in patients with anemia of chronic disease (inflammation).
NOX H94 is a pegylated Spiegelmer that specifically binds to human hepcidin, thereby
antagonizing its role in hemostasis, and is therefore indicated for use in anemia of
inflammation. Human hepcidin has emerged as the central regulatory molecule of systemic iron
homeostasis. Hepcidin expression in hepatocytes is regulated by multiple, in particular
opposing signals, including systemic iron availability, hepatic iron stores, erythropoietic
activity, hypoxia, and inflammatory states. These different signals are integrated
transcriptionally. In chronic inflammation, such as occurs in rheumatoid arthritis, chronic
kidney disease or cancer, elevated hepcidin levels have been measured and may be a key
factor leading to anemia in these patients.
NOX-H94 is therefore indicated for treatment of patients with an anemia of inflammation,
which is characterized by increased intracellular iron stores, increased serum ferritin
concentrations and reduced sensitivity to treatment with erythropoiesis stimulating agents
(ESAs), due to the limited availability of serum iron. Antagonism of hepcidin by NOX-H94
therefore leads to elevated levels of iron and transferrin saturation in the peripheral
blood and could supply iron for erythropoiesis thereby correcting the anemia.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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