| 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 |
| ATC code | S01LA05 |
| UNII | 15C2VL427D |
| KEGG | D09574 |
| Chemical data | |
| Formula | C4318H6788N1164O1304S32 |
| Mol. mass | 96.90 kDa |
| |
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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.
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]
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]
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