MVR-T3011 IT Intratumoral Injection Receives FDA Fast Track Designation for HNSCC Treatment
“Attaining Fast Track designation from the FDA marks a pivotal milestone and underscores MVR-T3011 IT’s capacity to address the substantial unmet needs of HNSCC patients,” said Grace Guoying Zhou, Chairwoman and CEO of ImmVira. “We are encouraged by the FDA’s decision as it reflects the need for FDA approved and widely available treatments for these patients. This designation will allow us to work closely with the FDA to quickly advance MVR-T3011 IT, to make a meaningful difference for patients who require new treatment options.”
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