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COMPANY RESEARCH

Silence Therapeutics

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.

Company at a glance

Corporate information

Company entity
Silence Therapeutics
Headquarters / principal office
LondonSelf-reported location on the company LinkedIn page; regional scope may differ from the legal or global headquarters. ↗
Founded
1994 (listed legal predecessor); renamed 2007 ↗
Ownership / capital status
Publicly tradedPublicly traded (Nasdaq: SLN); public-market transactions tracked separately ↗
LinkedIn company page
LinkedIn ↗ ↗

Profile review: 2026-11-04 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.

Disease tags match recorded text mentions and require program-level verification.

Technology, programs & evidence

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.

Individual program detail is not recorded. Consult the original sources below.

Related news & literature

Company-name matches are discovery leads; verify entity identity and transaction roles in the original source.

No cataloged update explicitly mentions this company.

Same-field reading (not company-specific)
Phio Pharmaceuticals

Phio schedules final PH-762 Phase 1b findings and plans Phase 2b in 2027

Phio announced a November 7 SITC oral presentation of final Phase 1b findings for intratumoral PH-762, its PD-1-silencing siRNA candidate, in cutaneous carcinomas. The company described tolerability and potential tissue-sparing neoadjuvant use, while stating that additional safety and efficacy studies are needed. A Phase 2b study is planned for the first half of 2027.

Vir Biotechnology / Business Wire

Vir schedules Phase 3 elebsiran–tobevibart results for The Liver Meeting

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.

Nature Communications

Peptide–oligonucleotide nanohybrids deliver miRNA to injured bone in rats

A Nature Communications study reports a peptide–oligonucleotide nanohybrid for bone-targeted miR-26a-5p delivery. The original abstract describes reduced GSK-3β expression and stabilization of HIF-1α, supporting coupled bone formation and angiogenesis. Systemic administration limited skeletal and vascular injury in a rat glucocorticoid-induced bone-loss model. This is preclinical miRNA delivery, not oral cyclic peptide therapy or human efficacy evidence.

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Sources & open questions

  • Company-level scope; current candidate stages, financing, site qualifications, and project suitability require separate verification.
  1. Silence Therapeutics — official disclosure ↗Silence Therapeutics · 2026-11-04 retrieval; page undated
  2. Company-managed LinkedIn profile — self-reported location ↗Silence Therapeutics · Checked 2026-11-04; source publication date retained where stated
  3. Founding / incorporation disclosure — scope stated in field ↗Silence Therapeutics · Checked 2026-11-04; source publication date retained where stated

Inclusion is not endorsement or partner qualification. Assess company claims, clinical evidence, and project-specific capabilities separately.

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