Chemistry:Diridavumab: Difference between revisions

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Latest revision as of 09:12, 8 February 2024

Short description: Monoclonal antibody

Diridavumab
Monoclonal antibody
Type	?
Source	Human
Target	hemagglutinin
Clinical data
Other names	CR6261
ATC code	none
Identifiers
CAS Number	1393659-46-5
ChemSpider	none
UNII	JFC86A9HL9
Chemical and physical data
Formula	C₆₄₀₀H₉₉₃₄N₁₇₀₂O₁₉₉₆S₄₈
Molar mass	144196.67 g·mol⁻¹

Diridavumab (CR6261) (INN^[1]) is a monoclonal antibody designed for the treatment of influenza A.^[2]

This drug was developed by Janssen Pharmaceutical Companies of Johnson & Johnson.

References

↑ World Health Organization (2014). "International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 111". WHO Drug Information 28 (2). https://www.who.int/medicines/publications/druginformation/innlists/PL111.pdf.
↑ Statement On A Nonproprietary Name Adopted By The USAN Council - Diridavumab, American Medical Association.

Monoclonal antibodies for infectious disease and toxins

Fungal ("-fung-")

Human ("-fungu-")	Efungumab^†

Viral ("-v(i)[r]-")

Human ("-viru-")	Diridavumab^§ Exbivirumab^§ Foravirumab^§ Libivirumab^§ Rafivirumab^§ Regavirumab^§ Sevirumab^† Suptavumab Tuvirumab^§
Chimeric ("-vixi-")	Cosfroviximab Larcaviximab Porgaviximab
Humanized ("-vizu-")	Felvizumab^§ Lenvervimab^† Motavizumab^† Palivizumab Suvizumab^§

Bacterial ("-ba(c)-")

Human ("-bacu-")	Nebacumab Panobacumab^§ Raxibacumab
Mouse ("-baco-")	Edobacomab^§
Chimeric ("-baxi-")	Pagibaximab^†
Humanized ("-bazu-")	Tefibazumab^†

Toxin ("-tox(a)-")

Human ("-toxu-")	Actoxumab^§ Bezlotoxumab Suvratoxumab
Chimeric ("-toxaxi-")	Obiltoxaximab
Humanized ("-toxazu-")	Urtoxazumab^§

^#WHO-EM
^‡Withdrawn from market
Clinical trials:
- ^†Phase III
- ^§Never to phase III

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