Axumin

— THERAPEUTIC CATEGORIES —
  • Imaging agents

Axumin Generic Name & Formulations

General Description

Fluciclovine F 18; 335–8200MBq/mL (9–221mCi/mL); soln for IV inj; preservative-free.

Pharmacological Class

Radioactive diagnostic agent.

How Supplied

Multi-dose vial (30mL, 50mL)—1

Generic Availability

NO

Mechanism of Action

Fluciclovine F 18 is a synthetic amino acid transported across mammalian cell membranes by amino acid transporters, such as LAT-1 and ASCT2, which are upregulated in prostate cancer cells. Fluciclovine F 18 is taken up to a greater extent in prostate cancer cells compared with surrounding normal tissues.

Axumin Indications

Indications

For positron emission tomography (PET) in males with suspected prostate cancer recurrence based on elevated blood prostate specific antigen (PSA) levels following prior treatment. 

Axumin Dosage and Administration

Adult

See full labeling. Give 370MBq (10mCi) as an IV bolus inj. Initiate imaging 3–5mins post-inj. 

Children

Not established.

Axumin Contraindications

Not Applicable

Axumin Boxed Warnings

Not Applicable

Axumin Warnings/Precautions

Warnings/Precautions

Have resuscitation equipment readily available. Risk for radiation exposure. Should only be used by trained and experienced physicians in the safe use and handling of radioactive materials to minimize radiation exposure. Risk for image misinterpretation and other errors. Not for use in females. 

Axumin Pharmacokinetics

Elimination

Renal. Half-life: 109.7 minutes.

Axumin Interactions

Not Applicable

Axumin Adverse Reactions

Adverse Reactions

Inj site pain, erythema, dysgeusia; hypersensitivity reactions. 

Axumin Clinical Trials

See Literature

Axumin Note

Not Applicable

Axumin Patient Counseling

See Literature