A Single Ascending Study of IOP Injection in Patients With Iron Deficient Anemia

Exclusion Criteria

• •1. Subject with known hemochromatosis, thalassemia, hemolytic anemia, receive red blood cell or whole blood transfusions within 90 days prior to enrollment.
• •2. Subject with a history of intravascular hemolysis.
• •3. Subject receiving any erythropoiesis-stimulating agent (ESA) therapy within 4 weeks prior to screenin.
• •4. Subject with a known sensitivity to any i.v. iron formulation
• •5. Subject with C-reactive protein \> 20 mg/dL.
• •6. Subject with HBV, HCV, HIV.
• •7. Subject with known malignancy or severe renal failure requiring dialysis.
• •8. Subject with a recent (within 1 year of study drug administration) drug or alcohol abuse (including cannabis products) as defined in Diagnostic and Statistical Manual of Mental Disorders, 4th edition, Diagnostic Criteria for Drug and Alcohol Abuse.
• •9. Subject averages an intake of more than 21 units of alcohol per week (≥ 3 drinks per day) for men and 14 units of alcohol per week (≥ 2 drinks per day) for women (1 unit of alcohol equals approximately 250 mL of beer, 100 mL of wine or 35 mL of spirits).
• •10. Subject who has smoked or used smoking cessation or nicotine containing products (including but not limited to e-cigarettes, pipes, cigars, chewing tobacco, nicotine patches, nicotine lozenges, or nicotine gum) within 6 months of the first dose of study drug.
• •11. Subject with any factor, which in the opinion of the Investigator would jeopardize the evaluation or safety or be associated with poor adherence to the protocol.
• •12. Subject with psychiatric disorder precluding the understanding of information on study related topics or giving informed consent.
• •13. Subject who has received another investigational agent within 4 weeks prior to screening.
• •14. Subject undergoing major surgery or physical trauma within 90 days or with major burn injury covering \> 20% of total body surface area.
• •15. Female subject who is pregnant or breast feeding.