FDA “Study May Proceed” Letter for (Z)-Endoxifen IND Application for Metastatic Breast Cancer Received
“This letter marks an important regulatory milestone for Atossa and to potentially expand the use of (Z)-endoxifen for metastatic ER+/HER2- Breast Cancer. We believe its activity, even in tumors that have developed resistance to other endocrine therapies and in the oncogenic signaling pathway, protein kinase C beta 1 (PKCβ1), may offer a new tool in treating this disease.,” said Dr. Steven Quay, M.D., Ph.D., Atossa Therapeutics President and Chief Executive Officer. “We appreciate the FDA’s review and look forward to advancing this clinical investigation.”
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