Lutathera

Active Ingredient(s): Lutetium Lu 177 Dotatate
FDA Approved: * January 26, 2018
Pharm Company: * ADVANCED ACCELERATOR APPLICATIONS USA INC
Category: Cancer

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Lutathera Overview

DOTA-TATE (DOTATATE,[1] DOTA-octreotate, oxodotreotide, DOTA-(Tyr3)-octreotate,[2] and DOTA-0-Tyr3-Octreotate) is an eight amino acid long peptide, with a covalently bonded DOTA bifunctional chelator. DOTA-TATE can be reacted with the radionuclides gallium-68, lutetium-177 and copper-64 to form radiopharmaceuticals for positron emission tomography (PET) imaging or radionuclide therapy. 177Lu DOTA-TATE therapy is a form of peptide receptor radionuclide therapy (...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/DOTA-TATE

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Possible Dosages for this and Related Drugs:

NDC Database Records for Lutathera: (1 result)

Sorted by National Drug Code

• 69488-003 Lutathera 10 mci/Ml Intravenous Injection by Advanced Accelerator Applications USA, Inc

Other drugs which contain Lutetium Lu 177 Dotatate or a similar ingredient: (1 result)

• LUTETIUM LU 177 DOTATATE