Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy regimen consists of intravenous iron sucrose and recombinant erythropoietin (typically epoetin alfa), used primarily for the treatment of anemia in patients with chronic kidney disease (CKD), including those not on dialysis. Iron sucrose is an intravenous iron replacement product that provides elemental iron for hemoglobin synthesis, addressing iron deficiency. Erythropoietin is a recombinant glycoprotein hormone that acts as an erythropoiesis-stimulating agent (ESA) by binding to erythropoietin receptors on red blood cell precursors in the bone marrow, stimulating their proliferation and differentiation. American Regent, Inc. (the U.S. marketer of Venofer) has been involved in clinical research evaluating the efficacy of this combination compared to oral iron supplements in managing renal anemia. This dual approach is designed to optimize red blood cell production by providing both the hormonal stimulus and the necessary iron substrate.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on iron sucrose + erythropoietin (American Regent, Inc.).