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

Stopped early · Phase 2

Conditions studied: Iron Deficiency Anemia

In brief

The purpose is to evaluate the efficacy and safety of IOP Injection (MPB-1514) for the treatment of iron-deficient anemia (IDA).

Key facts

Study ID: NCT03485053
Run by: MegaPro Biomedical Co. Ltd.
People needed: 49
Starts: 2018-11-29
Expected to finish: 2021-08-31
Last updated by the study team: 2021-10-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subject ≥ 18 years.
Subject with IDA but not secondary to any malignancy or renal failure requiring dialysis.
Hb levels <11.0 g/dL, Ferritin levels <200 ng/dL, Transferrin saturation (TSAT) < 20% at the Screening Visit.
Subject must have the ability to provide written, personally signed, and dated informed consent to participate in the study.
Subject must have an understanding, ability, and willingness to comply fully with study procedures and restrictions and to be available for clinic visits and follow-up procedures.
Female subject of child-bearing potential who is sexually active must use an effective method of birth control for at least one month prior to screening and agree to use an effective method of birth control until completion of participation in the study.

You may not qualify if…

Subject with known hemochromatosis, thalassemia, hemolytic anemia, receive red blood cell or whole blood transfusions within 90 days prior to enrollment.
Subject with a history of intravascular hemolysis.
Subject receiving any erythropoiesis-stimulating agent (ESA) therapy within 4 weeks prior to screenin.
Subject with a known sensitivity to any i.v. iron formulation
Subject with C-reactive protein > 20 mg/dL.
Subject with HBV, HCV, HIV.
Subject with known malignancy or severe renal failure requiring dialysis.
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.
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).
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.
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.
Subject with psychiatric disorder precluding the understanding of information on study related topics or giving informed consent.
Subject who has received another investigational agent within 4 weeks prior to screening.
Subject undergoing major surgery or physical trauma within 90 days or with major burn injury covering > 20% of total body surface area.
Female subject who is pregnant or breast feeding.

Where it is running

North America Research Institute — Azusa, California, United States
Valley Renal Medical Group — Northridge, California, United States
Whittier Internal Medicine and Nephrology Medical Group — Whittier, California, United States
South Florida Research Institute — Lauderdale Lakes, Florida, United States
North Shore University Hospital Lab — Manhasset, New York, United States
Clinical Research Development Associates — Springfield Gardens, New York, United States
Northeast Clinical Research Center — Bethlehem, Pennsylvania, United States
Southwest Houston Research Ltd. — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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