Phase 1 Study of the E-Selectin Inhibitor GMI 1070 in Patients with Sickle Cell AnemiaReport as inadecuate




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Background

Sickle cell anemia is an inherited disorder of hemoglobin that leads to a variety of acute and chronic complications. Abnormal cellular adhesion, mediated in part by selectins, has been implicated in the pathophysiology of the vaso-occlusion seen in sickle cell anemia, and selectin inhibition was able to restore blood flow in a mouse model of sickle cell disease.

Methods

We performed a Phase 1 study of the selectin inhibitor GMI 1070 in patients with sickle cell anemia. Fifteen patients who were clinically stable received GMI 1070 in two infusions.

Results

The drug was well tolerated without significant adverse events. There was a modest increase in total peripheral white blood cell count without clinical symptoms. Plasma concentrations were well-described by a two-compartment model with an elimination T1-2 of 7.7 hours and CLr of 19.6 mL-hour-kg. Computer-assisted intravital microscopy showed transient increases in red blood cell velocity in 3 of the 4 patients studied.

Conclusions

GMI 1070 was safe in stable patients with sickle cell anemia, and there was suggestion of increased blood flow in a subset of patients. At some time points between 4 and 48 hours after treatment with GMI 1070, there were significant decreases in biomarkers of endothelial activation sE-selectin, sP-selectin, sICAM, leukocyte activation MAC-1, LFA-1, PM aggregates and the coagulation cascade tissue factor, thrombin-antithrombin complexes. Development of GMI 1070 for the treatment of acute vaso-occlusive crisis is ongoing.

Trial Registration

ClinicalTrials.gov NCT00911495



Author: Ted Wun , Lori Styles, Laura DeCastro, Marilyn J. Telen, Frans Kuypers, Anthony Cheung, William Kramer, Henry Flanner, Seungshin

Source: http://plos.srce.hr/



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