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Sickle Cell & Hemoglobin

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Pursuing New Therapies Through Research

Physicians and researchers at Cincinnati Children's Hospital Medical Center conduct numerous clinical trials in hopes of improving the lives of patients with sickle cell disease and other hemoglobin disorders. Patients have the opportunity to participate in these studies, as well as in those offered at our site through organizations such as the National Heart, Lung and Blood Institute.

Outstanding laboratory research at Cincinnati Children’s provides the foundation for innovative clinical trials. Researchers at Cincinnati Children’s are exploring a variety of lab research initiatives.

  • Center director, Clinton H. Joiner, MD, PhD, is a world leader in studying the effects of sickle cell disease on red blood cell hydration. His work in the laboratory targets ways to improve water content in sickle red blood cells using drugs and genetic manipulation.
  • Theodosia A. Kalfa, MD, PhD, studies the structure of red blood cell membranes, how they are affected by sickle cells, and ways to improve membrane function in a variety of blood diseases.
  • Punam Malik, MD, and Ajay Perumbeti, MD, are working to develop gene therapy as a cure for sickle cell disease. They are exploring ways to remove a sickle cell patient’s blood-producing cells from the bone marrow, correct the sickle gene, and return the cells back into the bone marrow to stimulate production of normal hemoglobin.