Plus Therapeutics receives fast track designation from FDA for its novel glioblastoma treatment

Plus Therapeutics

15 September 2020 - Plus Therapeutics today announced that the U.S. FDA has granted the Company fast track designation for its lead investigational drug, Rhenium NanoLiposomes for the treatment of patients with recurrent glioblastoma. 

As previously reported, the Company also received orphan drug designation from the FDA for Rhenium NanoLiposomes for the treatment of patients with glioblastoma.

Read Plus Therapeutics press release

Michael Wonder

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Michael Wonder

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Cancer , Medicine , US , Fast track