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» FDA clears Chengdian (Suzhou) Biopharmaceutical’s IND for CD-001
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Immuno-oncology
FDA clears Chengdian (Suzhou) Biopharmaceutical’s IND for CD-001
Sep. 20, 2024
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Chengdian (Suzhou) Biopharmaceutical Co. Ltd. has received IND clearance from the FDA, allowing it to initiate a first-in-human phase I trial of CD-001.
BioWorld Science
Regulatory
Cancer
Antibody
Immuno-oncology
FDA
IND
