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See today's BioWorld MedTech
Home » US FDA resets review clock for Cyclopharm’s Technegas for pulmonary embolism
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US FDA resets review clock for Cyclopharm’s Technegas for pulmonary embolism

April 25, 2023
By Tamra Sami
After receiving a U.S. FDA complete response letter nearly two years ago, Cyclopharm Ltd. said the agency has accepted its response and reset the clock for the NDA review of its Technegas combination product for pulmonary embolisms, with a new PDUFA date set for Sept. 29.
BioWorld MedTech Cardiovascular Diagnostics U.S.

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