Research Project
8925781
DESCRIPTION (provided by applicant): SCD affects approximately 90,000 individuals, primarily African-Americans, in the United States. SCD patients suffer frequent recurrent pain crises precipitated by vaso-occlusion. The pain crises often result in serious complications leading to high morbidity and mortality in moderately to severely affected SCD patients. The only treatment option currently available to SCD patients is the FDA approved drug hydroxyurea (HU). Selexys is developing SelG1, a first in class humanized anti-P-selectin antibody, for the prophylactic treatment of vaso-occlusive sickle cell-related pain crisis in patients with SCD. The treatment goal is to prevent or reduce the frequency and duration of sickle cell-related pain crises. According to the applicant, preclinical data in mouse models of SCD have demonstrated a P-selectin dependent mechanism of cell adhesion between sickled red cells, activated endothelium, leukocytes and platelets that precipitates vaso-occlusion. In these models, administration of an anti-P-selectin antibody, or genetic deletion of P-selectin, prevents vaso-occlusion, supporting the rationale for blocking P-selectin in SCD patients. The applicant has completed a Phase 1 study using SelG1 in normal human volunteers that demonstrated that SelG1 was safe and well tolerated up to a multi-dose cohort of 8mg/kg. SelG1 was shown to have pharmacologic properties that support a once-monthly dosing strategy. Selexys proposes a Phase 2 study to assess the efficacy of SelG1 at high and low doses compared to placebo and obtain important safety and tolerability data on the chronic dosing of SelG1. The primary aim of this Phase 2 safety and efficacy study is to evaluate SelG1 as a prophylactic therapy to reduce or prevent the ongoing frequency and duration of sickle cell-related pain crises. Selexys was granted orphan drug designation status in July 2008 for SelG1 for the treatment of vaso-occlusive crisis in patient with SCD.
