The FDA has approved sarilumab (Kevzara) for the treatment of active polyarticular juvenile idiopathic arthritis (pJIA) in patients weighing 63 kg or greater, manufacturer Regeneron announced in a news release. The approval brings a new treatment option to pediatric patients with pJIA, which is a form of arthritis affecting multiple joints.
“Polyarticular juvenile idiopathic arthritis can be a painful disease for children where multiple joints are impacted by this chronic infammation,” George D. Yancopoulos, MD, PhD, board cochair, president, and chief scientific officer at Regeneron, said in a statement. "Not only are their daily lives impacted, but their futures can be disrupted without adequate treatment. The approval of [sarilumab] in polyarticular juvenile idiopathic arthritis provides these vulnerable patients and their families a new FDA-approved treatment option to help navigate this disease.”
The approval was supported by data from adequate, well-controlled studies in addition to pharmacokinetic data from adults with rheumatoid arthritis and a pharmacokinetic, pharmacodynamic, dose finding, and safety study conducted in pediatric patients with pJIA, according to the release.
Those with pJIA can be affected by joint pain, stiffness, and swelling, potentially restricting their activity and making daily life more difficult. Additionally, the chronic inflammation associated with pJIA increases the risk of permanent joint damage, delayed growth, and delayed development.
There were no new adverse reactions or safety concerns in the pJIA population vs the rheumatoid arthritis population, and the most common adverse drug reactions were nasopharyngitis, neutropenia, upper respiratory tract infection, and injection site erythema among those with pJIA. Neutropenia was the most common adverse reaction leading to permanent discontinuation of sarilumab.
Reference
Kevzara (sarilumab) approved by FDA for the treatment of active polyarticular juvenile idiopathic arthritis (PJIA). News release. Regeneron. June 11, 2024. Accessed June 11, 2024. https://investor.regeneron.com/news-releases/news-release-details/kevzarar-sarilumab-approved-fda-treatment-active-polyarticular
FDA Approves Tislelizumab-jsgr as First-Line Therapy for HER2– Gastric Cancers
January 2nd 2025Tislelizumab-jsgr (Tevimbra) was approved in combination with chemotherapy for the treatment of unresectable or metastatic HER2-negative (HER–) gastric or gastroesophageal junction adenocarcinoma (G/GEJ) in adults whose tumors express PD-L1.
Read More
ICYMI: Highlights From SPD 2024
December 30th 2024The Society for Pediatric Dermatology (SPD) Annual Meeting took place in Toronto, Canada, July 11-15, with our top coverage including the hot topics of combating misinformation and improving care for children with dermatologic conditions.
Read More
5 Key Drug Approvals and CRLs in 2024
December 27th 2024In 2024, multiple drugs received complete response letters (CRLs), sometimes unrelated to the safety and efficacy of the drug, but patients with schizophrenia gained the first new treatment with a new mechanism of action in decades.
Read More
First Subcutaneous Prophylaxis for Hemophilia A and B With Inhibitors Approved by FDA
December 23rd 2024The approval of concizumab-mtci (Alhemo) injection marks a significant milestone in managing hemophilia A and B with inhibitors by preventing or reducing bleeding episodes in adults and children 12 years and older.
Read More