What’s New
Explore latest events, medical insights and trends.
AAD 2026: Dermatology Updates Denver
AAD 2026 post-congress: Complete systemic therapy update. Multi-indication clinical data for inflammatory dermatological conditions.
Beyfortus® Real-World Effectiveness: Meta-Analysis
Systematic review shows Beyfortus® reduces RSV hospitalizations by 83% and ICU admissions by 81% in real-world infant immunization programs.
Expert consensus on the burden of RSV disease and the utility of nirsevimab for disease prevention and
protection of infants
Dupilumab in Chronic Spontaneous Urticaria: Evidence from the Phase 3 LIBERTY-CSU CUPID Trials
Chronic spontaneous urticaria (CSU) creates substantial patient burden through persistent wheals, angioedema, and debilitating itch that severely disrupts daily functioning. Emerging evidence positions type 2 inflammation as a driver of CSU pathogenesis. IL-4 plays a particularly crucial role by stimulating excessive IgE production and promoting formation of IgG anti-IgE autoantibodies—both pathways that trigger mast cell degranulation and subsequent CSU symptoms. This mechanistic understanding has opened therapeutic opportunities targeting type 2 inflammatory pathways for patients who remain symptomatic despite standard antihistamine therapy.
United in RARE: Advancing LSDs Care Across ASIA
The United in Rare: Advancing LSDs Care across Asia event was held on the 22nd to 23rd November 2025 in Bangkok, Thailand. The event aimed to provide a platform for experts across Thailand, Malaysia, Singapore, Taiwan, South Korea and India to share their experiences in management of LSDs by discussing challenges cases and best practices to improve diagnosis and treatment pathways for LSDs.
Attenuating the atopic march: Meta Analysis of The Dupilumab Atopic Dermatitis Database for Incident Allergic Events
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Rare diseases are more common than most people imagine
Rare Disease Day raises awareness for the 300 million people worldwide living with a rare disease, along with their families and carers. Over 6,000 rare diseases are characterized by a wide range of conditions and symptoms that can vary not only between diseases but also among individuals with the same condition. Take the opportunity to support equitable access to diagnosis, treatment, healthcare, social support for those affected by rare diseases.
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