Belatacept
Appearance
Clinical data | |
---|---|
Trade names | Nulojix |
AHFS/Drugs.com | Consumer Drug Information |
MedlinePlus | a606016 |
License data |
|
Routes of administration | Intravenous |
ATC code | |
Legal status | |
Legal status | |
Identifiers | |
ChemSpider |
|
UNII | |
(what is this?) (verify) |
Belatacept (trade name Nulojix) is a fusion protein composed of the Fc fragment of a human IgG1 immunoglobulin linked to the extracellular domain of CTLA-4,[2] which is a molecule crucial in the regulation of T cell costimulation, selectively blocking the process of T-cell activation. It is intended to provide extended graft and transplant[3] survival while limiting the toxicity generated by standard immune suppressing regimens, such as calcineurin inhibitors. It differs from abatacept (Orencia) by only 2 amino acids.
Belatacept was developed by Bristol-Myers-Squibb and approved by the U.S. Food and Drug Administration on June 15, 2011.[4]
References
- ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
- ^ "Healthvalue.net: CTLA-4 Strategies". Archived from the original on 5 December 2008. Retrieved 2008-10-24.
{{cite web}}
: Unknown parameter|deadurl=
ignored (|url-status=
suggested) (help) - ^ Vincenti, Flavio; Rostaing, Lionel; Grinyo, Joseph; Rice, Kim; Steinberg, Steven; Gaite, Luis; Moal, Marie-Christine; Mondragon-Ramirez, Guillermo A.; Kothari, Jatin; Polinsky, Martin S.; Meier-Kriesche, Herwig-Ulf; Munier, Stephane; Larsen, Christian P. (2016). "Belatacept and Long-Term Outcomes in Kidney Transplantation | NEJM". New England Journal of Medicine. 374 (4): 333–343. doi:10.1056/NEJMoa1506027. PMID 26816011.
- ^ "FDA approves Nulojix for kidney transplant patients" (Press release). U.S. Food and Drug Administration. 2011-06-15. Archived from the original on 19 June 2011. Retrieved 2011-06-16.
{{cite press release}}
: Unknown parameter|deadurl=
ignored (|url-status=
suggested) (help)