Flotufolastat F-18

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Short description: Medication
Flotufolastat F-18
Flotufolastat F-18 gallium
Clinical data
Trade namesPosluma
Other names18F-rhPSMA-7.3
License data
Routes of
administration
Intravenous
ATC code
  • None
Legal status
Legal status
Identifiers
CAS Number
PubChem CID
DrugBank
UNII
KEGG
Chemical and physical data
3D model (JSmol)

Flotufolastat F-18, sold under the brand name Posluma, is a radioactive diagnostic agent for use with positron emission tomography (PET) imaging for prostate cancer.[1] The active ingredient is flotufolastat F-18 gallium.[1]

Flotufolastat F-18 was approved for medical use in the United States in May 2023.[1][2]

Medical uses

Flotufolastat F-18 is indicated for positron emission tomography of prostate-specific membrane antigen positive lesions in men with prostate cancer.[1][3]

References

  1. 1.0 1.1 1.2 1.3 1.4 "Posluma- flotufolastat f-18 injection". 2 June 2023. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=907ac4a4-a088-4826-ab50-cfc31985c9d4. 
  2. "U.S. FDA Approves Blue Earth Diagnostics' Posluma (Flotufolastat F 18) Injection, First Radiohybrid PSMA-targeted PET Imaging Agent for Prostate Cancer" (Press release). Blue Earth Therapeutics. 30 May 2023. Retrieved 25 June 2023 – via Business Wire.
  3. "Flotufolastat F 18: Diagnostic First Approval". Molecular Diagnosis & Therapy 27 (5): 631–636. September 2023. doi:10.1007/s40291-023-00665-y. PMID 37439946. https://figshare.com/articles/online_resource/Flotufolastat_F_18_Diagnostic_First_Approval/23631417. 
  • Clinical trial number NCT04186819 for "Imaging Study to Investigate the Safety and Diagnostic Performance of rhPSMA 7.3 (18F) in Newly Diagnosed Prostate Cancer (LIGHTHOUSE)" at ClinicalTrials.gov
  • Clinical trial number NCT04186845 for "Imaging Study to Investigate Safety and Diagnostic Performance of rhPSMA 7.3 (18F) PET Ligand in Suspected Prostate Cancer Recurrence (SPOTLIGHT)" at ClinicalTrials.gov






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