USFDA halts Sun Pharma trials on dermatological drug Deuruxolitinib
The company said it would work closely with the FDA to address the agency's concerns, which the drugmaker expected to be communicated within the next 30 days.
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Bengaluru: The U.S. Food and Drug Administration (FDA) has asked India's Sun Pharmaceutical Industries Ltd to halt tests on one dose of an experimental dermatological drug due to the potential of blood clots, the company said on Tuesday.
The FDA has also said that patients with alopecia areata - an autoimmune condition that results in patchy hair loss - on the 12 mg dose of the drug deuruxolitinib should discontinue its use, Sun Pharma said.
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