FDA clearance to commence Ph 2 trial of leronlimab in patients with R/R microsatellite stable CRC
“We have appreciated the opportunity to work constructively with the FDA on the review and finalization of our CRC protocol,” said Dr. Jacob Lalezari, CEO of CytoDyn Inc. “With the agency’s input and our partnership with Syneos Health, we are well positioned to advance our clinical evaluation of leronlimab for oncology and make real strides towards developing the treatment paths of tomorrow.”
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