Entry ID | 2281 |
INN | Motavizumab |
Status | Terminated |
Drug code(s) | MEDI524 |
Brand name | Numax |
mAb sequence source | mAb humanized |
General Molecular Category | Naked monospecific |
Format, general category | Full length Ab |
Format details | None |
Isotype (Fc) | IgG1 |
Light chain isotype | kappa |
Linker | None |
Ave. DAR | None |
Conjugated/fused moiety | None |
Discovery method/technology | None |
Target(s) | RSV (F glycoprotein) |
Indications of clinical studies | Prevention of RSV infection in high risk infants |
Primary therapeutic area | Infectious diseases |
Most advanced stage of development (global) | Terminated at regulatory review |
Status | Inactive |
Start of clinical phase (IND filing or first Phase 1) | January 15, 2000 |
Start of Phase 2 | |
Start of Phase 3 | October 15, 2004 |
Date BLA/NDA submitted to FDA | |
Year of first approval (global) | None |
Date of first US approval | |
INN, US product name | None |
US or EU approved indications | None |
Company | AstraZeneca |
Licensee/Partner | None |
Comments about company or candidate | None |
Full address of company | Cambridge, United Kingdom Europe United Kingdom https://www.astrazeneca.com/our-company/contact-us.html |
Motavizumab, an affinity-optimized version of palivizumab, was developed to improve protection against RSV. These antibodies bind RSV F protein, which plays a role in virus attachment and mediates fusion. Described in J Virol. 2010 Aug;84(16):8132-40. doi: 10.1128/JVI.02699-09.
Anticipated events | None |
Factor(s) contributing to discontinuation | None |