From Surf Wiki (app.surf) — the open knowledge base
Rilonacept
Medication
Medication
| Field | Value | ||||
|---|---|---|---|---|---|
| type | |||||
| Verifiedfields | changed | ||||
| verifiedrevid | 464382495 | ||||
| tradename | Arcalyst | ||||
| Drugs.com | |||||
| licence_EU | yes | ||||
| DailyMedID | Rilonacept | ||||
| licence_US | |||||
| routes_of_administration | Subcutaneous | ||||
| ATC_prefix | L04 | ||||
| ATC_suffix | AC04 | ||||
| legal_AU | |||||
| legal_BR | |||||
| legal_CA | |||||
| legal_DE | |||||
| legal_NZ | |||||
| legal_UK | |||||
| legal_US | Rx-only | ||||
| legal_US_comment | |||||
| legal_EU | Rx-only | ||||
| legal_EU_comment | |||||
| legal_UN | |||||
| legal_status | |||||
| CAS_number_Ref | |||||
| CAS_number | 501081-76-1 | ||||
| DrugBank_Ref | |||||
| DrugBank | DB06372 | ||||
| ChemSpiderID_Ref | |||||
| ChemSpiderID | none | ||||
| UNII_Ref | |||||
| UNII | 8K80YB5GMG | ||||
| KEGG | D06635 | ||||
| ChEMBL_Ref | |||||
| ChEMBL | 1201830 | ||||
| synonyms | IL-1 Trap | ||||
| C | 9030 | H = 13932 | N = 2400 | O = 2670 | S = 74 |
| Drugs.com =
| elimination_half-life =
Rilonacept, sold under the brand name Arcalyst, is a medication used to treat cryopyrin-associated periodic syndromes, including familial cold autoinflammatory syndrome, and Muckle–Wells syndrome; deficiency of interleukin-1 receptor antagonist; and recurrent pericarditis. Rilonacept is an interleukin 1 inhibitor.
Rilonacept is a dimeric fusion protein consisting of the ligand-binding domains of the extracellular portions of the human interleukin-1 receptor component (IL-1R1) and IL-1 receptor accessory protein (IL-1RAcP) linked in-line to the fragment-crystallizable portion (Fc region) of human IgG1 that binds and neutralizes IL-1.
Rilonacept was given an orphan drug designation by the U.S. Food and Drug Administration (FDA) and is used for the treatment of cryopyrin-associated periodic syndromes (CAPS), including familial cold autoinflammatory syndrome, Muckle–Wells syndrome. Rilonacept is the first drug approved by the FDA to treat recurrent pericarditis. Rilonacept was approved for medical use in the United States in February 2008.
On May 8, 2012, an FDA Advisory Panel voted 11–0 against the approval of rilonacept for the treatment of gout, stating that the benefits did not outweigh the risks associated with the drug.
References
References
- "Arcalyst- rilonacept injection, powder, lyophilized, for solution".
- (17 September 2018). "Rilonacept Regeneron (previously Arcalyst) EPAR".
- (18 March 2021). "FDA Approves First Treatment for Disease That Causes Recurrent Inflammation in Sac Surrounding Heart".
- (October 2009). "The interleukin 1 inhibitor rilonacept in treatment of chronic gouty arthritis: results of a placebo-controlled, monosequence crossover, non-randomised, single-blind pilot study". Annals of the Rheumatic Diseases.
- (May 2008). "Molecule of the month. Rilonacept". Drug News & Perspectives.
- "Arcalyst FDA Approval History - Drugs.com".
- (2 May 2008). "Drug Approval Package: Arcalyst (Rilonacept) NDA #125249".
- (8 May 2012). "Medical News: FDA Panel Nixes Gout Drug - in Rheumatology, General Rheumatology from MedPage Today".
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Rilonacept — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report