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Cerianna FDA Approval History

Last updated by Judith Stewart, BPharm on June 24, 2020.

FDA Approved: Yes (First approved May 20, 2020)
Brand name: Cerianna
Generic name: fluoroestradiol F18
Dosage form: Injection
Company: Zionexa USA
Treatment for: Diagnosis and Investigation

Cerianna (fluoroestradiol F18) is a radioactive diagnostic agent indicated for use with positron emission tomography (PET) imaging for the detection of estrogen receptor (ER)-positive lesions as an adjunct to biopsy in patients with recurrent or metastatic breast cancer.

Development timeline for Cerianna

May 27, 2020Approval FDA Approves Cerianna (fluoroestradiol F18) PET Imaging Agent for Use in Patients with Recurrent or Metastatic Breast Cancer

Further information

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