Asset Manager

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Eliem Therapeutics

Eliem Therapeutics is a Redmond-based clinical-stage biotech led by CEO Aoife Brennan, developing ETX-155 for depression after a 2024 pipeline reset.

Eliem Therapeutics

Eliem Therapeutics is a US-based company founded in 2018 in Redmond. It focuses on developing treatments for nervous system disorders. The company has secured $291.3 million in total funding.

General information

Firm type

Asset Manager

Year founded

2018

AUM

Undisclosed

Location

Region

North America

Country

United States

City

Redmond

Corporate office

Redmond, WA, United States

Additional offices

Cambridge, United Kingdom

Principals

Aoife Brennan

Chief Executive Officer

Sector focus

Digital HealthHealthcare Services

Frequently asked questions

Who runs investment and strategic decisions at Eliem Therapeutics?

CEO Aoife Brennan leads all strategic and capital-allocation decisions. She was appointed to the role in 2024 following the company's pipeline restructure and the $120 million private placement. Brennan previously served as CEO of Synlogic, a synthetic biology company, and has an MD from Trinity College Dublin. The board, reshaped after the 2024 financing, includes representatives from RA Capital and other life-science investors who influence capital planning.

What is Eliem Therapeutics' current pipeline?

Eliem's clinical pipeline consists of a single asset: ETX-155, an oral prodrug of allopregnanolone. The company is initially developing ETX-155 for perimenopausal depression, with a Phase 2 clinical trial that dosed its first patient in January 2025. Allopregnanolone is a neuroactive steroid that modulates GABA-A receptors, a well-validated mechanism in mood disorders. Prior pipeline programs in neuronal excitability, including a depression candidate that failed a Phase 2 trial, were discontinued in 2024.

How is Eliem Therapeutics funded?

Eliem completed a $120 million private placement in April 2024, led by RA Capital Management, which recapitalized the company following the failure of its previous lead program. The company is publicly traded on Nasdaq under the ticker ELYM, but the private placement brought in a largely new institutional shareholder base. As a clinical-stage company with no approved products, Eliem does not generate revenue and relies entirely on equity financing to fund operations.

Does Eliem Therapeutics collaborate with external research partners?

Eliem acquired the global rights to ETX-155 through a research collaboration, though the company has not publicly named the originating partner. The firm maintains a research presence in Cambridge, UK, which suggests ongoing ties to the European neuroscience research community. Beyond this, Eliem has not disclosed active academic or industry partnerships as of 2025.

What is the relationship between Eliem Therapeutics and RA Capital Management?

RA Capital Management led the $120 million private placement that recapitalized Eliem in April 2024 and subsequently gained representation on the company's board. The relationship is that of a lead institutional investor, not a parent or controlling entity. The financing essentially re-founded the company around a new strategy, new CEO, and new board, with RA Capital as the anchor investor.

Is Eliem Therapeutics a family office, venture firm, or operating company?

Eliem Therapeutics is a publicly traded clinical-stage biotechnology company, not a family office or investment firm. It develops its own drug candidates and does not invest in external companies or manage third-party capital. The firm's Nasdaq listing (ELYM) and single-asset focus distinguish it from diversified asset managers or venture platforms.

What are the key binary events for Eliem Therapeutics?

The single most consequential event is the Phase 2 readout for ETX-155 in perimenopausal depression. The trial began dosing patients in January 2025, and the company has not yet guided on a data readout timeline. A positive result would likely trigger a follow-on financing or partnership discussions; a negative result would challenge the company's viability. No other clinical catalysts are publicly disclosed.

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