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Silence Therapeutics
Silence Therapeutics was founded in 1994 as a spinout from research into RNA interference, a field then in its earliest infancy.
Silence Therapeutics
Silence Therapeutics was founded in 1994 as a spinout from research into RNA interference, a field then in its earliest infancy. It originally listed on the London Stock Exchange's AIM market in 2005 before moving to the main market and, in 2020, securing a Nasdaq listing. Craig Tooman became CEO in 2021, replacing Mark Rothera, whose tenure had navigated a complex merger with InteRNA Technologies that consolidated the Berlin research site. The wealth origin is not a single-family source; the firm is a publicly traded clinical-stage company whose equity is held by institutional investors, not a family office. The firm's strategy is concentrated: develop short interfering RNA (siRNA) therapies that silence disease-causing genes in the liver. Its platform, mRNAi GOLD, uses GalNAc conjugation for targeted delivery to hepatocytes. The pipeline spans hematology and cardiovascular conditions. The lead asset, zerlasiran, is in Phase 3 for elevated lipoprotein(a) — a genetically-driven risk factor for atherosclerotic cardiovascular disease with no approved therapies. Silence out-licensed regional rights to zerlasiran to AstraZeneca for an upfront payment of $20 million in 2020, and to Hansoh Pharma for Greater China in 2021, each deal carrying milestone payments up to $1.3 billion and $1.3 billion respectively. Other disclosed programs include divesiran for polycythemia vera, a Phase 1/2 asset wholly owned, and an earlier-stage iron-chelation program targeting thalassemia and myelodysplastic syndromes. The geographic footprint is European R&D with an American capital base: the Berlin lab drives discovery science, while the London and New York listings fund it. Total deployment is not measured by AUM but by cash runway and R&D spend. As of its 2024 annual report, the firm held over £100 million in cash and equivalents, with a research and development burn rate of approximately £30 million annually. The team size is not publicly fixed in a single portrait, but operations span the London headquarters and the Berlin laboratory. In January 2025, Silence announced a $10 million equity investment from a leading institutional healthcare investor to extend the runway for divesiran's Phase 2 readout. This was not a fund close but a strategic equity placement — a signal that the firm finances itself through public-market raises and licensing deals rather than drawing from a single family's pool of capital. The genuine structural differentiator is Silence's embedded relationship with the largest pharma licensing machine in RNA therapies — AstraZeneca, which itself bet big on the modality through the Alexion acquisition. A small-cap biotech running a Phase 3 program with a top-10 pharma partner while holding full US rights to a wholly owned Phase 2 asset is a rare posture. This is not a family office; it's a publicly traded drug developer whose governance rests with a board and shareholders, not a family council. The company's survival has always depended on proving its siRNA chemistry can be industrialized against materially larger competitors like Alnylam — a pressure that shapes every budget decision and partnership term sheet.
General information
Firm type
Asset Manager
Year founded
1994
AUM
Undisclosed
Location
Region
Europe
Country
United Kingdom
City
London
Corporate office
London, United Kingdom
Additional offices
Berlin, Germany
Principals
Craig Tooman
CEO
Sector focus
Frequently asked questions
Is Silence Therapeutics structured as a family office?
No. Silence Therapeutics is a publicly traded clinical-stage biopharmaceutical company listed on both the Nasdaq and the London Stock Exchange. It develops RNA interference therapies using its own proprietary platform and is funded by equity markets, licensing partnerships, and institutional investors. It does not manage the wealth of a single family or individual.
Who controls investment and strategic decisions at Silence Therapeutics?
Strategic and capital-allocation decisions are made by CEO Craig Tooman and the board of directors, with ultimate accountability to public shareholders under UK and US securities regulations. The firm is not governed by a family council or a single principal. Major pipeline moves and partnership terms are disclosed per London and Nasdaq listing rules.
What is Silence Therapeutics' most advanced drug asset and who partners on it?
The lead asset is zerlasiran, a siRNA therapy that targets the LPA gene to reduce lipoprotein(a) levels. It is currently in Phase 3 clinical trials. Silence out-licensed regional rights to AstraZeneca for most global markets and to Hansoh Pharma for Greater China, retaining rights in certain territories while earning milestone payments and royalties on future sales (per the firm, 2020–2021).
How does Silence Therapeutics source its drug candidates?
Silence generates its own pipeline internally using the mRNAi GOLD platform, a proprietary technology for designing and delivering GalNAc-conjugated siRNAs to hepatocytes. The firm does not acquire external programs; preclinical and clinical assets come from internal discovery work run out of its Berlin laboratory (per the firm's scientific publications and pipeline disclosures).
Does Silence Therapeutics deploy capital into funds or co-invest in other companies?
No. Silence is an operating biotechnology company. It deploys its cash into its own drug discovery, clinical trials, and platform science — not into venture capital funds, private equity, or direct co-investments alongside external GPs. Its treasury serves to fund research and development and general corporate purposes.
What does the licensing structure with AstraZeneca and Hansoh Pharma mean for Silence's balance sheet?
The partnership structures provide non-dilutive capital through upfront payments and potential milestone payments. The $20 million upfront from AstraZeneca in 2020 and subsequent economics from the Hansoh deal supplement equity raises. Future clinical, regulatory, and sales milestones could total up to $1.3 billion per deal, with tiered royalties on net sales in licensed territories (per the firm, 2020–2021).
Which diseases does Silence Therapeutics explicitly not target?
The firm focuses exclusively on diseases with validated liver-expressed gene targets where GalNAc-mediated siRNA delivery applies. It does not pursue central nervous system disorders, solid tumors outside hepatocyte biology, or non-genetic targets. Its public pipeline is confined to hematology, cardiovascular disease, and iron-overload disorders — a deliberate exclusion of wider therapeutic areas (per the firm's pipeline disclosures).
Profile maintained by Altss using OSINT (open-source intelligence), regulatory filings, licensed data partners, and verified direct submissions. Read the methodology. Last updated: . Continuous refresh with full update cycles at least every 30 days.
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