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seven drugs awaiting approval in 2025

Seven drugs slated for approval in 2025 could revolutionize treatment for various rare diseases. These include diazoxide choline for Prader-Willi syndrome, fitusiran for hemophilia, elamipretide for Barth syndrome, nipocalimab for myasthenia gravis, plozasiran for familial chylomicronemia syndrome, sebetralstat for hereditary angioedema, and taletrectinib for ROS1-positive non-small cell lung cancer. These drugs aim to improve the lives of those with rare conditions, demonstrating recent advancements in research, diagnosis, and treatment.

Source: www.labiotech.eu –

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