FDA grants Fast Track Designation to MYTX-011 for Patients with NSCLC with cMET Overexpression
“Receiving Fast Track designation from the FDA reinforces our focus on addressing the unmet need of patients living with cMET-positive NSCLC, who currently have few effective treatments,” said Brian Fiske, PhD, Chief Scientific Officer and Co-Founder at Mythic Therapeutics. “We are proud of this significant milestone as it highlights the potential of MYTX-011, which is enabled by our FateControl™ platform, to expand ADC therapy to more NSCLC patients.”
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