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Find Clinical Drug Pipeline Developments & Deals by Keros Therapeutics
KER-050 (elritercept) is an engineered ligand trap comprised of a modified ligand-binding domain of the TGF-ß receptor known as activin receptor type IIA. It is being developed for Lower-Risk Myelodysplastic Syndromes.
The net proceeds will be used to advance the development of KER-050, an investigational, modified activin receptor type IIA ligand, in two Phase 2 clinical trials, one in patients with myelodysplastic syndromes and one in patients with myelofibrosis.
The net proceeds will be used to advance the development of KER-050, an investigational, modified activin receptor type IIA ligand, in two Phase 2 clinical trials, one in patients with myelodysplastic syndromes and one in patients with myelofibrosis.
KER-065 is a novel ligand trap designed to bind to and inhibit TGF-ß ligands, including myostatin (GDF8) and activin A. It is being evaluated for the treatment of obesity.
KER-047, is designed to selectively and potently inhibit ALK2, a TGF-β receptor. KER-047 is being developed for the treatment of functional iron deficiency which is a consequence of elevated ALK2 signaling, including the Company’s initial target, IRIDA.
KER-047, is designed to selectively and potently inhibit activin receptor-like kinase-2, a TGF-β superfamily receptor. KER-047 is being developed for the treatment of functional iron deficiency which is a consequence of elevated ALK2 signaling.
KER-012 is designed to bind to and inhibit the signaling of transforming growth factor-beta (“TGF-β”) ligands that suppress bone growth, including activin A and activin B.
Keros believes that KER-012 (“RKER-012”) has the potential to increase the signaling of bone morphogenic protein (“BMP”) pathways through this inhibition of activin A and activin B signaling, and consequently treat diseases.
KER-050, is an engineered ligand trap comprised of a modified ligand-binding domain of the transforming growth factor-beta receptor known as activin receptor type IIA that is fused to the portion of the human antibody known as the Fc domain.
KER-012 is designed to bind to and inhibit the signaling of TGF-ß ligands that suppress bone growth, including activin A and activin B. KER-012 is being developed for the treatment of PAH and for the treatment of disorders associated with bone loss.
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