Celularity (CELU) Receives Orphan Drug Designation from U.S. FDA for its NK Cell Therapy CYNK-101
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Celularity Receives Orphan Drug Designation from U.S. FDA for its NK Cell Therapy CYNK-101 in Development for the First-Line Treatment of Advanced HER2/neu Positive Gastric and Gastroesophageal Juncti
February 15, 2022 4:05 PM ESTCYNK-101 is an investigational genetically modified NK cell therapy designed to synergize with antibody therapeutics for difficult to treat cancers of high unmet medical need
Phase 1/2a clinical trial will evaluate the safety and preliminary efficacy of CYNK-101 in combination with standard chemotherapy, trastuzumab and pembrolizumab as a first-line treatment in advanced HER2/neu positive gastric and gastroesophageal junction cancer
Fifth designation received by Celularity within twelve months from the FDA
FLORHAM PARK, N.J., Feb. 15, 2022 (GLOBE... More
