Supporting the Development of Nucleic Acid-Based Medicines
Oligonucleotide therapeutics—including antisense oligonucleotides (ASOs), small interfering RNA (siRNA), and aptamers—represent a rapidly maturing class of medicines designed to precisely modulate gene expression at the nucleic acid level. By directly targeting RNA through sequence specific interactions, these modalities enable therapeutic strategies that are not accessible with traditional small molecules or biologics, offering new paths to address genetic and metabolic diseases. Chemically synthesized oligonucleotides inherently generate closely related impurities - such as N‑1 and N+1, failure sequences, and protecting group variants - that can differ by a minor modification.