Only half of cancer medicines approved by the European Medicines Agency in 20202023 are available in EU countries (on average) Average time from EMA approval to patient access: 586 days, with major variation between Member States Access to biomarker testing, essential for personalised cancer treatment, is inconsistent across Europe Reducing disparities in access to medicines and diagnostics is essential to ensure innovation benefits all patients, wherever they live
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Current clinical trials and future directions Several clinical trials are expanding the potential uses of GLP-1 drugs
It supports healthy skin, may improve skin complexion, pigmentation and help with skin brightening
