Key Facts

Framework

• Investigator-initiated registry hosted by non for profit organization (UNEV)
• Academia-driven (supported by GA²LEN, EADV and WAO, endorsed by GA²LEN, EAACI and EADV Task Forces for Chronic Urticaria)
• Cooperation with stakeholders (industry, patient organizations, payers, health authorities)
• Open to all urticaria-treating physicians
• International approach: The registry will be launched initially in Germany, Spain, France, Italy and UK. Later it will be extended to the rest of Europe, USA, Canada, Brazil, India, China and Japan, etc.

Key Features of CURE

• Web-based-registry
• Basic data (Physician module) – entered once (30 minutes)
• Follow up data (Physician module) – entered every 6 months (15 minutes)
• Patient module (in preparation)

Recruitment Plan

• 1^st year: 250-500 new patients
• 2^nd year: 500-1000 new patients
• 3^rd year: >1000 new patients