Potential for once-daily oral administration
Data from prior preclinical and clinical studies in non-PV patients demonstrated consistent, dose-dependent, and reversible hematocrit reductions
Potential for red-cell selectivity, novel MOA, without additional cytotoxicity, pan-myelosuppression, or drug-drug interactions, with flexible titration
Polycythemia vera (PV) drives overproduction of red blood cells, raising hematocrit and the risk of thrombosis, cardiovascular events, and disease progression. The goal is straightforward: keep hematocrit controlled.

Epetraborole works through an entirely different pathway than existing therapies. It selectively modulates red cell production at the source — without broadly suppressing white cells, platelets, or other hematologic lineages. This erythroid selectivity is the core of its differentiation: targeted hematocrit control, not generalized cytoreduction.
Prior clinical data in non-PV patients consistently demonstrate dose-dependent, reversible hematocrit reductions beginning within weeks of treatment, with white cell and platelet counts remaining stable and within normal ranges throughout.