FDA Fast-Tracks KST-6051 for Advanced Solid Tumors
“FDA Fast Track designation for KST-6051 is an important regulatory milestone for Kestrel, based on the strength of our preclinical data package. This designation will allow us to work more closely with the FDA as we advance KST-6051 through our ongoing Phase 1 study, with the goal of bringing a much needed treatment option to patients with KRAS-mutant tumors as efficiently as possible,” said Frank Haluska, MD, PhD, President and Chief Executive Officer of Kestrel Therapeutics.
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