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Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

CERIANNA

FLUOROESTRADIOL F-18 Positron Emitting Activity
Oncology Approved 2020-05-20
1
Indication
--
Phase 3 Trials
5
Years on Market

Details

Status
Prescription
First Approved
2020-05-20
Routes
INTRAVENOUS
Dosage Forms
SOLUTION

Companies

Active Ingredient: FLUOROESTRADIOL F-18

CERIANNA Approval History

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What CERIANNA Treats

1 indications

CERIANNA is approved for 1 conditions since its original approval in 2020. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Breast Cancer
Source: FDA Label

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

CERIANNA FDA Label Details

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Indications & Usage

FDA Label (PDF)

CERIANNA is 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. CERIANNA 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. Limitations of Use Tissue biopsy should be used to confirm recurrence of breast cancer and to verify ER status by pathology. CERIAN...

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.