Chemistry:Lampalizumab
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Short description: Monoclonal antibody
Monoclonal antibody | |
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Type | Fab fragment |
Source | Humanized (from mouse) |
Target | CFD |
Clinical data | |
Routes of administration | Intravitreal |
ATC code |
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Identifiers | |
CAS Number | |
IUPHAR/BPS | |
ChemSpider |
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UNII | |
KEGG | |
Chemical and physical data | |
Formula | C2068H3214N546O676S13 |
Molar mass | 46958.39 g·mol−1 |
Lampalizumab (INN) is an antigen-binding fragment of a humanized monoclonal antibody that binds to complement factor D; it was developed as a potential treatment of geographic atrophy (atrophy of the retinal cells, retinal pigment epithelium, and choriocapillaris) secondary to age-related macular degeneration.[1][2]
One of the two Phase 3 clinical trials (Spectri) was interrupted on September 8, 2017 due to failure to meet primary end point.[3] The second Phase 3 clinical trial (Chroma) also failed to meet its primary end point.[4]
These two failures have called into question whether complement inhibition is a sound strategy for geographic atrophy.[5]
References
- ↑ World Health Organization (2012). "International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 107". WHO Drug Information 26 (2). https://www.who.int/medicines/publications/druginformation/innlists/Final_PL107.pdf.
- ↑ "Statement On A Nonproprietary Name Adopted By The USAN Council - Lampalizumab". American Medical Association. http://www.ama-assn.org/resources/doc/usan/lampalizumab.pdf.
- ↑ "Roche provides update on first lampalizumab phase III study for geographic atrophy, an advanced form of age-related macular degeneration" (in en). http://www.roche.com/investors/updates/inv-update-2017-09-08b.htm.
- ↑ "Statement on Chroma Study" (in en). https://www.roche.com/media/store/statements.htm.
- ↑ "Age-related macular degeneration foils drugmakers". Nature Biotechnology 35 (11): 1000–1001. November 2017. doi:10.1038/nbt1117-1000. PMID 29121027.
Original source: https://en.wikipedia.org/wiki/Lampalizumab.
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