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The company’s proprietary assay effectively mitigates heterophilic antibody interference to precisely measure a critical impurity.
April 6, 2026
By: Patrick Lavery
Content Marketing Editor
GC Biopharma has developed and validated a proprietary enzyme-linked immunosorbent assay (ELISA) to lessen an impurity linked to thromboembolic risks. The ELISA effectively mitigates heterophilic antibody interference in order to precisely measure levels of the critical impurity Factor XI (FXI). GC Biopharma characterizes the assay’s validation as a significant step forward in safety monitoring of intravenous immunoglobulin (IVIG). Significance of Thromboembolic Events IVIG therapy may ...
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