EMA Proposes Guidance On Oligonucleotide Drugs Amid Growing Role In Personalized Medicine

The draft guidance addresses specific requirements for oligonucleotide-based medicines that are not answered in existing guidance documents, and has been two years in the making.

Guidelines
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The European Medicines Agency has drafted scientific guidance for the development and manufacture of oligonucleotide drugs, on which it is seeking feedback via a public consultation that is open until 31 January 2025.

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