Fluorodopa F 18

(Fluorodopa F 18®)

Fluorodopa F 18

Drug updated on 9/5/2024

Dosage Forminjectable (intravenous; 15.5 MBq/mL to 308.2 MBq/mL [0.42 mCi/mL to 8.33 mCi/mL])
Drug ClassRadioactive diagnostic agents
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for use in positron emission tomography (PET) to visualize dopaminergic nerve terminals in the striatum for the evaluation of adult patients with suspected Parkinsonian syndromes (PS). Fluorodopa F 18 PET is an adjunct to other diagnostic evaluations.

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Summary
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  • Fluorodopa F 18 (fluorodopa F 18) is indicated for use in positron emission tomography (PET) to visualize dopaminergic nerve terminals in the striatum for the evaluation of adult patients with suspected Parkinsonian syndromes (PS). Fluorodopa F 18 PET is an adjunct to other diagnostic evaluations.
  • This summary is based on the review of four systematic review(s)/meta-analysis(es). [1-4]
  • Juvenile Parkinsonism (JP) and Dopamine Responsive Dystonia (DRD): Fluorodopa (FD) PET scans showed significantly decreased uptake in the putamen and caudate nucleus in JP patients, while DRD patients exhibited uptake patterns similar to normal subjects with only slight reductions.
  • Brain Tumors (Gliomas): 18F-FDOPA PET was more effective than 18F-FDG PET/CT in managing gliomas, demonstrating utility across stages, including diagnosis, grading, treatment assessment, and prognosis. The studies focused on glioma patients without detailed subgroup analysis.
  • Recurrent Medullary Thyroid Carcinoma (MTC): F-DOPA PET outperformed FDG PET and other radiopharmaceuticals in detection rates for recurrent MTC, showing the highest effectiveness regardless of serum calcitonin or CEA levels and calcitonin doubling time.
  • There is no safety information available in the reviewed studies.
  • There is no population types or subgroups information available in the reviewed studies.