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6 company, guide, and curated content matches · plus news and online publication results
…tions Research guide ↗ Oligonucleotide Therapeutics & Delivery Follow siRNA, ASOs, splice modulation, conjugation, delivery, analytics, and manufacturing. Research questions & evidence boundaries Research guide ↗ In Vivo Cell Engineering & Gene Editing Explore in vivo CAR-T, nonviral editing deliver…
…tions Research guide ↗ Oligonucleotide Therapeutics & Delivery Follow siRNA, ASOs, splice modulation, conjugation, delivery, analytics, and manufacturing. Research questions & evidence boundaries Research guide ↗ In Vivo Cell Engineering & Gene Editing Explore in vivo CAR-T, nonviral editing deliver…
Silence Therapeutics develops siRNA medicines through its mRNAi GOLD platform. The name refers to RNA interference and gene silencing; it should not be classified as an mRNA-expression platform. Silence Therapeutics develops siRNA medicines through its mRNAi GOLD platform. The name refers to RNA int…
…ctober 27, 2026 update describes WVE-007 as an investigational GalNAc-siRNA and WVE-006 as an investigational RNA-editing oligonucleotide. These are distinct modalities, not mRNA products. Wave develops RNA-targeting medicines using RNA interference and RNA editing approaches. Its October 27, 2026 u…
… registrational WVE-006 RNA-editing study in AATD and ongoing WVE-007 siRNA Phase 2a work. The company also reports FDA support for its LC-MS assay in the planned WVE-006 program. Regulatory feedback and trial plans do not constitute marketing approval or comparative efficacy evidence. Wave季度更新介绍AAT…
Vir Biotechnology announced that Phase 3 ECLIPSE 1 results for elebsiran plus tobevibart in chronic hepatitis delta will be presented on November 8, with an investor discussion on November 9. Elebsiran is an HBV-targeting siRNA; tobevibart is an antibody. The release announces the forthcoming readout and expanded Phase 2 presentations but does not disclose the Phase 3 numerical results.
An AAPS Open perspective surveys conjugation strategies for antisense oligonucleotides and siRNAs, including small-molecule ligands, cell-penetrating peptides, antibodies, and aptamers. The abstract contrasts clinically established GalNAc delivery with emerging approaches to extrahepatic tissues and discusses translation challenges. This is a synthesis of delivery platforms and clinical progress, rather than a new experimental or clinical efficacy study.
Wave's quarterly update describes planning for a registrational WVE-006 RNA-editing study in AATD and ongoing WVE-007 siRNA Phase 2a work. The company also reports FDA support for its LC-MS assay in the planned WVE-006 program. Regulatory feedback and trial plans do not constitute marketing approval or comparative efficacy evidence.