Comanche Biopharma Announces FDA Clearance of Investigational New Drug (IND) Application for CBP-4888, an siRNA Investigational Therapy for the Treatment of Preeclampsia
Excerpt from the Press Release:
CONCORD, Mass., March 30, 2023 /PRNewswire/ — Comanche Biopharma Corp., a biopharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) has cleared an investigational new drug (IND) application for Comanche’s novel, siRNA therapy to treat preeclampsia. Preeclampsia is a prevalent hypertensive disorder of pregnancy for which there is no existing therapy that can modify disease progression.
“The FDA’s clearance of CBP-4888 allows us to take another major step toward developing a treatment for preeclampsia,” said Scott Johnson, M.D., Co-Founder and CEO of Comanche Biopharma. “We will now move expeditiously into a first-in-human clinical trial to evaluate this potential therapy.”
CBP-4888 is a subcutaneously delivered siRNA therapeutic that decreases the production of soluble fms-like tyrosine kinase-1 (sFLT1) in the placenta.
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