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Keros Therapeutics

Keros Therapeutics, founded in 2015 by Jasbir Seehra, targets TGF-beta signaling to treat rare blood disorders and pulmonary arterial hypertension.

Keros Therapeutics

Keros Therapeutics launched in 2015, emerging from the discovery that controlled modulation of transforming growth factor-beta (TGF-beta) ligands could address the root causes of hematologic and musculoskeletal diseases. Founder Jasbir Seehra, a biochemist who previously held senior roles at Acceleron Pharma, structured the company around protein therapeutics engineered to bind specific TGF-beta family members without the off-target toxicities that derailed earlier industry attempts. The founding scientific insight — targeting activin receptor type IIA and IIB signaling — shaped a pipeline now centered on rare blood disorders and cardiovascular disease. Keros' most advanced program is KER-050, or elritercept, an activin receptor type IIA-Fc fusion protein designed to treat cytopenias by promoting late-stage red blood cell and platelet production. It is in Phase 2 trials for myelodysplastic syndromes and myelofibrosis, including a registrational trial initiated in 2023 for transfusion-dependent anemia. A second candidate, KER-012, targets activin receptor type IIB to reduce the elevated TGF-beta signaling that drives vascular remodeling in pulmonary arterial hypertension, with Phase 2 data expected in 2025. The pipeline also includes KER-065, a dual inhibitor of activin A and myostatin, in Phase 1 for Duchenne muscular dystrophy and obesity-related muscle loss. Keros operates discovery and clinical operations from its Lexington, Massachusetts headquarters. In December 2021, the company entered a licensing agreement with Hansoh Pharmaceutical Group for development and commercialization across Greater China, securing an upfront payment and potential milestones exceeding $1 billion. The company reported 166 full-time employees at year-end 2023 and has funded operations through public equity offerings and the Hansoh partnership rather than private venture rounds. Its 2020 IPO on Nasdaq raised $96 million, followed by a $160 million follow-on offering in February 2023 that extended the cash runway into 2027. Keros is not a family office, fund, or asset allocator — it is a clinical-stage biopharmaceutical company that raises capital through equity markets and partnership agreements, with R&D expense representing the primary use of proceeds. Founder Seehra and the scientific leadership maintain deep ties to the Dana-Farber Cancer Institute and the broader Boston biotech ecosystem where the original TGF-beta biology was elucidated. Keros occupies a specific structural niche in TGF-beta drug development: while large pharmaceutical companies have largely abandoned broad TGF-beta inhibition due to cardiac toxicity, Keros' approach targets individual ligands with engineered Fc-fusion proteins that act as decoy receptors rather than blocking antibodies. This ligand-trap architecture, developed by Seehra and his co-founders from Acceleron, offers a cleaner selectivity profile than predecessor molecules. The company has not established related investment vehicles or philanthropic foundations separate from its corporate structure, and its governance follows a standard public-company model with a five-member board that included CEO Seehra and representatives from Orbimed Advisors and Foresite Capital at the time of the company's IPO.

General information

Firm type

Asset Manager

Year founded

2015

AUM

Undisclosed

Location

Region

North America

Country

United States

City

Lexington

Corporate office

Lexington, MA, United States

Principals

Jasbir S. Seehra

President and Chief Executive Officer

Sector focus

BiotechnologyHealthcare Services

Frequently asked questions

How does Keros Therapeutics' drug design differ from previous TGF-beta inhibitors?

Keros develops engineered Fc-fusion proteins that act as decoy receptors, selectively binding individual TGF-beta family ligands like activin A and GDF-11. This ligand-trap approach avoids the broad TGF-beta receptor blockade that caused cardiac toxicity in earlier antibody programs from large pharmaceutical companies. The selectivity profile was inherited from the intellectual property and scientific team Seehra developed at Acceleron Pharma.

What is Keros' lead clinical asset and what does it treat?

Keros' lead candidate is KER-050, or elritercept, an activin receptor type IIA-Fc fusion protein. It targets cytopenias — dangerously low blood cell counts — in myelodysplastic syndromes and myelofibrosis by promoting late-stage red blood cell and platelet production. A registrational Phase 2 trial in transfusion-dependent anemia initiated in late 2023.

What was the Hansoh Pharmaceutical partnership structure?

In December 2021, Keros granted Hansoh Pharma exclusive rights to develop and commercialize KER-050 in Greater China. Keros received an undisclosed upfront payment and is eligible for development and commercial milestone payments potentially exceeding $1 billion, plus tiered royalties on net sales. The deal does not cover global territories outside Greater China, which Keros retains.

How is Keros financed and what is its capital runway?

Keros is a publicly traded biotech that raised $96 million in its April 2020 IPO and completed a $160 million follow-on equity offering in February 2023. At year-end 2023, the company reported cash and cash equivalents sufficient to fund operations through 2027. It has not raised private venture rounds since the public listing.

Does Keros operate as a family office or investment vehicle?

No. Keros Therapeutics is a clinical-stage biopharmaceutical company incorporated in Delaware and operated from Lexington, Massachusetts. It is not structured as a family office, fund, or family investment vehicle. Its capital comes from public equity markets and corporate partnerships, deployed entirely toward drug development operations.

What are the next clinical data catalysts for Keros?

Keros expects to report Phase 2 data from the KER-012 program in pulmonary arterial hypertension during 2025 and from the KER-050 registrational trial in transfusion-dependent anemia on an ongoing basis. The Phase 1 trial of KER-065 in Duchenne muscular dystrophy is also advancing, with initial data anticipated in 2025.

Who are the key scientific leaders behind Keros Therapeutics?

Founder and CEO Jasbir Seehra led discovery research at Acceleron Pharma, where the foundational TGF-beta superfamily biology was developed. The scientific team includes individuals with deep ties to Dana-Farber Cancer Institute and the Boston biotech cluster. The company's approach builds directly on the ligand-trap engineering that Acceleron deployed before its acquisition by Merck in 2021.

Profile maintained by 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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