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Actinium faces potential securities fraud investigation after FDA deems Phase 3 trial insufficient, causing stock drop.
Actinium Pharmaceuticals faces a potential securities fraud investigation by Pomerantz LLP following a negative FDA update on its planned BLA filing for Iomab-B in r/r AML.
The Phase 3 SIERRA trial was deemed insufficient for BLA filing.
After the announcement, Actinium's stock dropped 59.81%.
Pomerantz LLP advises investors to contact them for further info.
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Actinium enfrenta una posible investigación de fraude de valores después de que la FDA considere que el ensayo de Fase 3 es insuficiente, causando una caída de las existencias.