Active Ingredient(s): Olaratumab
FDA Approved: * October 19, 2016
Pharm Company: * ELI LILLY AND CO
Category: Cancer

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

Lartruvo Overview

Olaratumab, sold under the brand name Lartruvo, is a monoclonal antibody medication developed by Eli Lilly and Company for the treatment of solid tumors. It is directed against the platelet-derived growth factor receptor alpha.[1] It was removed from the United States and European Union markets in 2019, due to insufficient proof of its medical advantage (see below "Medical uses"). Contents 1 Medical uses 2 Contraindications 3 Side effects 4 Interactions 5 Pharmacology 5.1 M...

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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:

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Possible Dosages for this and Related Drugs:

  • Injection: 500mg/50ml, 500mg/50ml(10mg/ml)
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Lartruvo: (2 results)

Sorted by National Drug Code
  • 0002-7190 Lartruvo 10 mg/ml Intravenous Injection, Solution by Eli Lilly and Company
  • 0002-8926 Lartruvo 10 mg/ml Intravenous Solution by Eli Lilly and Company

Other drugs which contain Olaratumab or a similar ingredient: (1 result)