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Lumicell shines a light on residual breast cancer with FDA approvals

Lumicell Inc. sees a brighter future now that it has secured U.S. FDA approval for both its new drug application for Lumisight (pegulicianine) optical imaging agent and premarket approval for the Lumicell direct visualization system . The company markets the two together as the Lumisystem to detect and resect residual breast cancer. Newton, Mass.-based Lumicell expects the Lumisystem will be available in the fourth quarter of 2024, Lumicell President and Chief Operating Officer Howard Hechler told BioWorld. ....

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FDA delivers approval to Lumicell's fluorescent system for highlighting residual breast cancer tissue

FDA delivers approval to Lumicell's fluorescent system for highlighting residual breast cancer tissue
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FDA Approves Drug-Device Combo to Detect Residual Cancer After Lumpectomy

The FDA has approved Lumisight (pegulicianine), an optical imaging agent, to illuminate residual breast cancer. ....

Howard Hechler , Drug Administration , Lumicell Direct Visualization System , Chief Operating Officer ,

Lumicell's Cutting-Edge Imaging Platform Receives Historic FDA Approval to Illuminate Residual Breast Cancer

Lumicell's Cutting-Edge Imaging Platform Receives Historic FDA Approval to Illuminate Residual Breast Cancer
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FDA Approves Lumisight and Lumicell DVS for Residual Breast Cancer Detection

The FDA has approved the optical imaging agent Lumisight and the Lumicell Direct Visualization System for use in fluorescence imaging in breast cancer. ....

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