FDA Approves Pediatric Risankizumab - Report - MDSpire
Advertisement
FDA Approves Pediatric Risankizumab
Approval expands risankizumab use to pediatric plaque psoriasis and psoriatic arthritis and includes a new 55-mg prefilled syringe for weight-based dosing in patients weighing less than 40 kg.
Clinical Report: FDA Approves Pediatric Risankizumab
Overview
The FDA has approved risankizumab for pediatric patients aged 6 years and older with moderate to severe plaque psoriasis and active psoriatic arthritis. This approval includes a new 55-mg prefilled syringe for patients weighing less than 40 kg.
Background
Psoriasis and psoriatic arthritis can significantly impact the quality of life in pediatric patients, with approximately 30% of psoriasis cases beginning before age 18.
Data Highlights
The pediatric plaque psoriasis indication is supported by the phase 3 OptIMMize clinical trial program, which included various cohorts of patients aged 6 to 18 years.
Key Findings
Risankizumab is the first IL-23 inhibitor approved for pediatric patients aged 6 years and older in the US.
The approval includes a 55-mg prefilled syringe for patients weighing less than 40 kg.
Approximately 20,000 children under 10 years are diagnosed with psoriasis annually in the US.
The safety profile in pediatric patients is consistent with that observed in adults.
At Week 16, risankizumab demonstrated clinically meaningful improvements in psoriasis severity measures.
Clinical Implications
Healthcare providers should monitor patients for infections and tuberculosis prior to initiating treatment.
Conclusion
The FDA has approved risankizumab for pediatric use.