FDA Approves Cablivi For Rare Blood Clotting Disorder essay is one as concers the Health and Medical Updates categories, posted at our publisher Linda Norton just as February 7, 2019, those article maybe want to search just after these tags approves, Bloodclotting, cablivi, disorder, FDA, rare. I am pleasant to glad you along with providing those anothers paper like health also I always updating the post daily.
(HealthDay)—Cablivi (caplacizumab-yhdp) injection has been approved by the U.S. Food and Drug Administration to treat adults with acquired thrombotic thrombocytopenic purpura (aTTP).
“Patients with aTTP endure hours of treatment with daily plasma exchange, which requires being attached to a machine that takes blood out of the body and mixes it with donated plasma and then returns it to the body,” Richard Pazdur, M.D., director of the FDA Oncology Center of Excellence, said in a statement. “Even after days or weeks of this treatment, as well as taking drugs that suppress the immune system, many patients will have a recurrence of aTTP.”
Cablivi is the first targeted treatment that inhibits blood clot formation and provides a new treatment option for patients that may reduce recurrences. Cablivi was evaluated in clinical studies involving 145 people. Those treated with Cablivi had fewer instances of aTTP-related death, the FDA said.
Common side effects include headache and bleeding of the nose or gums. Cablivi’s prescribing information includes a warning about the risk for severe bleeding. Health care providers should closely monitor patients who also take anticoagulants, the FDA said.
The drug is produced by Ablynx, based in Belgium.
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FDA approves cablivi for rare blood-clotting disorder (2019, February 7)
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