FDA Clearance for Ph I Clinical Trial of CD-001 Announced
“The FDA’s clearance of this IND reinforces our unwavering commitment to advancing groundbreaking immunotherapies.” said Dr. Jian Xu, CEO of CDBiopharma. “CD-001 shows promise as a first-in-class and best-in-class treatment, and preclinical studies have demonstrated its effectiveness in various mouse tumor models, with excellent tolerance observed in non-human primates. We are excited to move forward with patient enrollment and expect initial clinical data in the upcoming months.”
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