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Aflibercept
Clinical data
Trade names Eylea, Zaltrap
Licence data US FDA:link
Pregnancy cat. C (US)
Legal status -only (US)
Routes Injection
Identifiers
CAS number 862111-32-8 N
ATC code S01LA05
UNII 15C2VL427D YesY
KEGG D09574 YesY
Chemical data
Formula C4318H6788N1164O1304S32 
Mol. mass 96.90 kDa
 N (what is this?)  (verify)

Aflibercept is a fusion protein approved in the United States for the treatment of wet macular degeneration and metastatic colorectal cancer.

It is an inhibitor of vascular endothelial growth factor.[1][2] It is designed to bind to VEGF-A, VEGF-B, and placental growth factor (a.k.a PIGF, gene symbol PGF).[3]

Aflibercept is being co-developed by Sanofi-Aventis and Regeneron Pharmaceuticals.

Approvals and indications [edit]

In November 2011 the United States Food and Drug Administration approved aflibercept for the treatment of wet macular degeneration.[4]

On August 3, 2012 the United States Food and Drug Administration approved Zaltrap (ziv-aflibercept) for use in combination with 5-fluorouracil, leucovorin and irinotecan to treat adults with metastatic colorectal cancer that is resistant to or has progressed following an oxaliplatin‑containing regimen.[5]

In November 2012 the European Medicines Agency (EMA) approved aflibercept for the treatment of wet macular degeneration.[6]

Clinical trials [edit]

In March 2011 Regeneron reported that aflibercept failed its primary endpoint of overall survival in the Vital phase III trial for second-line treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC), although it improved the secondary endpoint of progression-free survival.[3][7]

In April 2011 Regeneron reported that aflibercept improved its primary endpoint of overall survival in the Velour phase III clinical trial for second-line treatment for metastatic colorectal cancer (mCRC).[3]

Aflibercept is also in a phase III trial for hormone-refractory metastatic prostate cancer.[3]

References [edit]


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