Lartruvo

Product manufactured by Eli Lilly And Company

Application Nr Approved Date Route Status External Links
BLA761038 None Intravenous None Google , Wikipedia , PubMed , DailyMed , Raw OpenFDA , ECHA , ToxNet , JECFA , FAO , 21 CFR

Indications and Purposes

1 Indications And Usage Lartruvo™ Is Indicated, In Combination With Doxorubicin, For The Treatment Of Adult Patients With Soft Tissue Sarcoma (sts) With A Histologic Subtype For Which An Anthracycline-Containing Regimen Is Appropriate And Which Is Not Amenable To Curative Treatment With Radiotherapy Or Surgery. This Indication Is Approved Under Accelerated Approval [see Clinical Studies ( 14 )] . Continued Approval For This Indication May Be Contingent Upon Verification And Description Of Clinical Benefit In The Confirmatory Trial. Lartruvo™ Is A Platelet-Derived Growth Factor Receptor Alpha (pdgfr-Α) Blocking Antibody Indicated, In Combination With Doxorubicin, For The Treatment Of Adult Patients With Soft Tissue Sarcoma (sts) With A Histologic Subtype For Which An Anthracycline-Containing Regimen Is Appropriate And Which Is Not Amenable To Curative Treatment With Radiotherapy Or Surgery. ( 1 ) This Indication Is Approved Under Accelerated Approval. Continued Approval For This Indication May Be Contingent Upon Verification And Description Of Clinical Benefit In The Confirmatory Trial. ( 14 )

All Formulated Excipients (0 Total)

None

Active Ingredients ( 1 Total)

Name Structure ZINC ID(s)
1. Olaratumab

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