FDA clearance granted to begin Ph 1/2a trial in the U.S. for CKD-703
“With FDA approval to initiate this trial, we are accelerating global development to position CKD-703 as a best-in-class therapy,” a Chong Kun Dang spokesperson said. “This is our first ADC oncology candidate, developed by integrating our proprietary antibody technology with global ADC platform innovations.”
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