Lanadelumab demonstrates rapid and sustained prevention of hereditary angioedema attacks

التفاصيل البيبلوغرافية
العنوان: Lanadelumab demonstrates rapid and sustained prevention of hereditary angioedema attacks
المؤلفون: Jonathan A. Bernstein, Aleena Banerji, Marcus Maurer, Peng Lu, Salome Juethner, H. Henry Li, Hilary Longhurst, James Hao, Marc A. Riedl, William R. Lumry, Help Study Investigators
المصدر: Allergy
Allergy, vol 75, iss 11
بيانات النشر: Wiley, 2020.
سنة النشر: 2020
مصطلحات موضوعية: medicine.medical_specialty, Allergy, onset of action, Immunology, Attack rate, Atopic Dermatitis, Urticaria and Skin Disease, HELP Investigators, Lanadelumab, Antibodies, Monoclonal, Humanized, Placebo, Antibodies, long‐term prophylaxis, symbols.namesake, Internal medicine, Monoclonal, Humans, Immunology and Allergy, Medicine, Poisson regression, Time to onset, Adverse effect, Humanized, business.industry, Angioedemas, Hereditary, Angioedemas, medicine.disease, hereditary angioedema, long-term prophylaxis, Hereditary, Treatment Outcome, Hereditary angioedema, symbols, Original Article, durable efficacy, Onset of action, ORIGINAL ARTICLES, business, Complement C1 Inhibitor Protein
الوصف: Background Lanadelumab demonstrated efficacy in preventing hereditary angioedema (HAE) attacks in the phase 3 HELP Study. Objective To assess time to onset of effect and long‐term efficacy of lanadelumab, based on exploratory findings from the HELP Study. Methods Eligible patients with HAE type I/II received lanadelumab 150 mg every 4 weeks (q4wks), 300 mg q4wks, 300 mg q2wks, or placebo. Ad hoc analyses evaluated day 0‐69 findings using a Poisson regression model accounting for overdispersion. Least‐squares mean monthly HAE attack rate for lanadelumab was compared with placebo. Intrapatient comparisons for days 0‐69 versus steady state (days 70‐182) used a paired t test for continuous endpoints or Kappa statistics for categorical endpoints. Results One hundred twenty‐five patients were randomized and treated. During days 0‐69, mean monthly attack rate was significantly lower with lanadelumab (0.41‐0.76) vs placebo (2.04), including attacks requiring acute treatment (0.33‐0.61 vs 1.66) and moderate/severe attacks (0.31‐0.48 vs 1.33, all P ≤ .001). More patients receiving lanadelumab vs placebo were attack free (37.9%‐48.1% vs 7.3%) and responders (85.7%‐100% vs 26.8%). During steady state, the efficacy of lanadelumab vs placebo was similar or improved vs days 0‐69. Intrapatient differences were significant with lanadelumab 300 mg q4wks for select outcomes. Lanadelumab efficacy was durable—HAE attack rate was consistently lower vs placebo, from the first 2 weeks of treatment through study end. Treatment emergent adverse events were comparable during days 0‐69 and 70‐182. Conclusion Protection with lanadelumab started from the first dose and continued throughout the entire study period.
During days 0‐69, lanadelumab‐treated patients had a significantly lower mean monthly hereditary angioedema (HAE) attack rate vs placebo and were more likely to be responders and attack free. Protection starts early and is sustained; during steady state, lanadelumab efficacy was similar or improved vs days 0‐69. Prophylactic agents with rapid onset, sustained effect, and convenient dosing frequency can improve HAE management plans. Abbreviations: HAE, hereditary angioedema; q2wks, every 2 weeks.
وصف الملف: application/pdf
تدمد: 1398-9995
0105-4538
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa6235c902377cd5373f0ecd7b907e6a
https://doi.org/10.1111/all.14416
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....aa6235c902377cd5373f0ecd7b907e6a
قاعدة البيانات: OpenAIRE