_plus-therapeutics-receives-fda-orphan-drug-designation-for-its-novel-glioblastoma-treatment.jpg "Plus Therapeutics Receives FDA Orphan Drug Designation for its Novel Glioblastoma Treatment from said benefits rates Video Screenshot Preview")
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⏲ Duration: 37 sec
✓ Published: 21-Nov-2020
✓ Published: 21-Nov-2020
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Austin, Texas, Sept. 01, 2020 -- Plus Therapeutics, Inc. (Nasdaq: PSTV) (the “Company”), today announced that the U.S. Food and Drug Administration (FDA) has granted the Company orphan drug designation (https://www.accessdata.fda.gov/script...) for its lead investigational drug, Rhenium NanoLiposomes (RNL™) for the treatment of patients with recurrent glioblastoma. nnRNL is being evaluated in the NIH/NCI-supported, multi-center ReSPECT™ Phase 1 dose-finding clinical trial (NCT01906385)(h
Austin, Texas, Sept. 01, 2020 -- Plus Therapeutics, Inc. (Nasdaq: PSTV) (the “Company”), today announced that the U.S. Food and Drug Administration (FDA) has granted the Company orphan drug designation (https://www.accessdata.fda.gov/script...) for its lead investigational drug, Rhenium NanoLiposomes (RNL™) for the treatment of patients with recurrent glioblastoma. nnRNL is being evaluated in the NIH/NCI-supported, multi-center ReSPECT™ Phase 1 dose-finding clinical trial (NCT01906385)(h
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