NICE has issued a positive recommendation for Sobi's Kineret (anakinra) to be used as a first-line biologic therapeutic option for Still’s disease.
The UK’s National Institute for Health and Care Excellence (NICE) has issued a positive recommendation for Kineret (anakinra) to be used as a first-line biologic therapeutic option for Still’s disease.
In a March 31, 2021 press release, Kineret drug company, Sobi, revealed the recommendation, which also covers systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s Disease (AOSD). Still’s disease is a rare, serious inflammatory disorder that can present in adults as AOSD or children up to 16 years old as sJIA.
“We are pleased to receive this positive news for anakinra,” said Michael Oliver, vice-president and general manager, Sobi UK and Republic of Ireland, in the press release. “As a company we are committed to improving the lives of people with rare diseases and this recommendation will provide earlier access to anakinra in patients with Still’s disease and help to enhance their quality of life.”
“I welcome this positive recommendation for anakinra in relation to sJIA, as it offers an effective, therapeutic option for a disease which can be associated with significant morbidity among patients,” commented Professor A Ramanan, consultant pediatric rheumatologist, Bristol Royal Hospital for Children, in the press release.
“This final NICE guidance endorses that clinicians have the flexibility to use anakinra earlier in the patient pathway, as a first-line biologic therapy, which is something specialists in this area welcome and brings us closer to quicker disease control that would prevent progressive joint and systemic damage,” added Paul Brogan, professor of vasculitis and speciality lead, Paediatric Rheumatology, Great Ormond Street Hospital Institute for Child Health, in the press release.
Source: Sobi
Regeneron Treatment for Multiple Myeloma Gets Conditional Marketing Approval from EC
April 29th 2025The indication is specific to patients who have received at least three prior therapies, including a proteasome inhibitor, immunomodulatory agent, and anti-CD38 monoclonal antibody, and have demonstrated disease progression on the last therapy.
MHRA Approves GSK Therapy Combinations for Multiple Myeloma
April 21st 2025Belantamab mafodotin is approved in combination with bortezomib plus dexamethasone in patients who have had at least one prior therapy, and in combination with pomalidomide plus dexamethasone for those who have had a prior therapy including lenalidomide.