Clinical development failure
KER-065 and elritercept are still in clinical trials, so efficacy or safety setbacks could eliminate value.
- Scope
- KER-065, elritercept, and other pipeline assets
- Materiality
- high
Keros Therapeutics is a clinical-stage biopharmaceutical company developing protein therapeutics for disorders driven by dysfunctional TGF-β family signaling. Its pipeline is centered on KER-065 for neuromuscular disease and elritercept for cytopenias such as anemia and thrombocytopenia in MDS and myelofibrosis.
28,3 %
35,7 %
15.45
15.45
| % | |
|---|---|
| Clinical-stage product candidates | 0% Protein therapeutics in human trials, including KER-065 and elritercept. |
| Discovery and preclinical programs | 0% Earlier-stage programs such as cibotercept and related pipeline research. |
| Collaboration and license revenue | 100% Upfront, milestone, and potential royalty income from partners such as Takeda. |
| Contracted manufacturing and supply chain services | 0% CMO-based manufacturing, labeling, packaging, and distribution for clinical supply. |
Keros does not sell approved commercial products; its current counterparties are pharmaceutical partners and clinical...
Partners such as Takeda pay upfronts, milestones, and future royalties to access Keros assets and development rights.
Sites and patients participate in trials for KER-065, elritercept, and other programs to generate clinical data.
Patients with neuromuscular disease, MDS, or myelofibrosis would be the eventual users if products are approved.
Hospitals, specialists, and reimbursement systems would influence adoption and access after commercialization.
Keros is headquartered in Lexington, Massachusetts and operates as a U.S.-based development company...
Keros is focused on advancing its clinical pipeline while using partnerships to fund development and broaden reach...
The program is a key value driver and needs human data to support future partnering or approval.
The deal provides non-dilutive capital and external development capacity while preserving royalty upside.
If any candidate is approved, Keros will need manufacturing, sales, and distribution capabilities.
Patent and know-how protection are central to exclusivity and partnering leverage in biotech.
Keros remains a development-stage biotech with no approved products, so its value depends on clinical success,...
KER-065 and elritercept are still in clinical trials, so efficacy or safety setbacks could eliminate value.
The company has a limited operating history and expects substantial ongoing R&D spending.
Clinical and future commercial supply depend on CMOs with no redundant supply arrangements in place.
Large biotech and pharma companies can outspend Keros and regulatory requirements may change.
A meaningful portion of revenue is tied to the Takeda collaboration and its milestone/royalty path.
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: 28/04/2026