Sutimlimab Shows Promise for Hard-to-Treat, Rare Blood Disorder
Therapy Improves Severe Hemolytic Anemia in Cold Agglutinin Disease
(WASHINGTON, December 17, 2018) – In a first-in-human clinical trial reported today in Blood, the investigational drug sutimlimab appeared to be effective in treating cold agglutinin disease, a rare chronic blood disorder for which there are currently no approved treatments.
Cold agglutinin disease is caused by a malfunction in the immune system that causes antibodies––components of the immune system that are produced in the blood and help the body fight off disease–– to mistakenly latch onto and kill red blood cells. The disease is a type of hemolytic anemia, a condition that occurs when the bone marrow can’t produce red blood cells as quickly as they are destroyed.
In the study, sutimlimab, a specific C1s inhibitor, rapidly halted the destruction of red blood cells, increased hemoglobin levels, eliminated patients’ need for blood transfusions, and caused no serious adverse effects.
“The drug was well tolerated, produced clinically meaningful increases in hemoglobin levels, and precluded the need for transfusions, even in patients for whom multiple prior therapies had failed,” said senior author Bernd Jilma, MD, of the Medical University of Vienna.
Cold agglutinin disease is thought to affect about 10,000 people in the United States and Europe. Most patients with the disease are over 50 years old.
To date, there are no U.S. Food and Drug Administration (FDA)-approved treatments for cold agglutinin disease, though rituximab— a treatment for certain blood cancers — has been used with or without chemotherapy with limited success.
This study included 10 patients 56-76 years old. Patients had cold agglutinin disease for a median of five years, and many had received multiple prior treatments that had been unsuccessful. At enrollment, all patients had below-normal levels of hemoglobin, a component of red blood cells that is responsible for transporting oxygen to cells and organs throughout the body. Six patients were receiving regular blood transfusions to control their symptoms.
Of those patients who responded, within the first week of treatment with a full dose of sutimlimab, destruction of red blood cells stopped and patients’ hemoglobin levels significantly increased, said Dr. Jilma. Seven patients responded and had a median increase in hemoglobin levels of 4 grams per deciliter (g/dL) over a baseline of 7.5 g/dL within six weeks. Four patients had their hemoglobin levels return to normal.
When sutimlimab treatment was discontinued and the drug had left the patients’ blood, hemoglobin levels dropped and destruction of red blood cells began again. However, when treatment resumed, these effects were once again reversed. The six patients who had been sustained by regular blood transfusions remained transfusion-free for up to 18 months while receiving sutimlimab treatment.
“Provided that safety results remain positive, sutimlimab could become the first approved treatment for cold agglutinin disease,” Dr. Jilma said. “The drug clearly addresses an unmet medical need, as we have seen rapid, strong responses in patients for whom multiple prior therapies have failed.”
Sutimlimab has been given Breakthrough Therapy Designation by the U.S. Food and Drug Administration. Phase III studies are ongoing to determine its safety and efficacy in primary cold agglutinin disease patients.
This study was supported by True North Therapeutics, Inc. (now part of Bioverativ Inc., a Sanofi company). For more information about the sutimlimab phase III studies, visit clinicaltrials.gov (study numbers: NCT03347396 and NCT03347422).
Blood (www.bloodjournal.org), the most cited peer-reviewed publication in the field of hematology, is available weekly in print and online. Blood is a journal of the American Society of Hematology (ASH) (www.hematology.org), the world’s largest professional society concerned with the causes and treatment of blood disorders.
ASH’s mission is to further the understanding, diagnosis, treatment, and prevention of disorders affecting blood, bone marrow, and the immunologic, hemostatic, and vascular systems by promoting research, clinical care, education, training, and advocacy in hematology.
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