Only days after the Food and Drug Administration cleared Diatide's acute venous thrombosis imaging agent AcuTect (SCAN 9/30/98), the Londonderry, NH, radiopharmaceutical firm received a $2 million milestone payment from marketing partner Nycomed Amersham
Only days after the Food and Drug Administration cleared Diatide's acute venous thrombosis imaging agent AcuTect (SCAN 9/30/98), the Londonderry, NH, radiopharmaceutical firm received a $2 million milestone payment from marketing partner Nycomed Amersham of Buckinghamshire, U.K. The cash is the second payment Diatide has received from Nycomed Amersham in the last two months: In August, Diatide received $2 million for filing a new drug application for NeoTect, its lung cancer imaging agent.
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Study Shows Enhanced Diagnosis of Coronary Artery Stenosis with Photon-Counting CTA
July 10th 2025In a new study comparing standard resolution and ultra-high resolution modes for patients undergoing coronary CTA with photon-counting detector CT, researchers found that segment-level sensitivity and accuracy rates for diagnosing coronary artery stenosis were consistently > 89.6 percent.
FDA Expands Approval of MRI-Guided Ultrasound Treatment for Patients with Parkinson’s Disease
July 9th 2025For patients with advanced Parkinson’s disease, the expanded FDA approval of the Exablate Neuro platform allows for the use of MRI-guided focused ultrasound in performing staged bilateral pallidothalamic tractotomy.