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Lerdelimumab is a human monoclonal antibody developed as an immunosuppressive agent targeting transforming growth factor beta 2 (TGF beta 2). Its primary mechanism of action is the inhibition of TGF beta 2, a cytokine involved in fibrotic processes. Lerdelimumab was investigated for reducing scarring after glaucoma drainage surgery and showed potential activity in other ocular diseases such as cataract, retinopathy, and connective tissue diseases. The drug was granted European orphan drug status for preventing scar formation post-glaucoma surgery but development was discontinued after unsuccessful clinical trial results[1][3][6][8].
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