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It was developed by Novo Nordisk in 2012
Phase 3 trials are planned for 2025
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Ongoing investments in new production facilities, peptide synthesis reactors, purification systems, and key raw materials such as Fmoc amino acids, resins, and coupling reagents are expected to further strengthen global manufacturing capacity and support the long-term growth of the market
People who use these products are therefore at a very high risk of treatment failure, unexpected and serious health problems and dangerous interactions with other medicines. This week, the EMA reminded consumers that prescription medicines should be taken under the supervision of a healthcare professional and that their online sale is barred in many member states
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