FDA clears IND application for cancer therapeutic IMT-009
1 day ago - By Healio
FDA cleared an investigational new drug application for IMT-009, a fully human monoclonal antibody that combats inhibitory T-cell target CD161, according to a company press release.
The IND clearance applies to patients who are refractory to standard-of-care therapy, or ineligible for or refused another existing treatment option.
The clearance of IMT-009 indicates the continuation of recent developments of cell therapy in cancer treatment.
“We are thrilled to advance IMT-009 to the clinic as we believe it represents a new wave of immuno-oncology agents with
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Target Time and Superquiz, Monday, September 26
Trivia buffs: test your knowledge with today's interactive superquiz and target.
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