Entry ID | 1958 |
INN | Pagibaximab |
Status | Terminated |
Drug code(s) | BSYX-A110, hu96-110 |
Brand name | None |
mAb sequence source | mAb chimeric |
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) | Staphylococcal lipoteichoic acid |
Indications of clinical studies | Staphylococcal Sepsis in very low birth weight neonates |
Primary therapeutic area | Infectious diseases |
Most advanced stage of development (global) | Terminated at Phase 2/3 |
Status | Inactive |
Start of clinical phase (IND filing or first Phase 1) | July 02, 2001 |
Start of Phase 2 | March 15, 2003 |
Start of Phase 3 | |
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 | Sunol Molecular |
Licensee/Partner | Biosynexus Incorporated, GSK |
Comments about company or candidate | None |
Full address of company | 2810 N COMMERCE PKY, MIRAMAR, FL 33025, United States North America United States of America https://www.sbir.gov/node/320095 |
Target is “Staphylococcal lipoteichoic acid” according to https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2704668/
Anticipated events | None |
Factor(s) contributing to discontinuation | None |