Celularity Gets FDA Clearance of IND Application for CYNK-101 in Gastric Cancer
November 29 2021 - 8:58AM
Dow Jones News
By Michael Dabaie
Celularity Inc. said the U.S. Food and Drug Administration
cleared its Investigational New Drug application for CYNK-101 in
combination with standard chemotherapy, trastuzumab and
pembrolizumab in advanced Her2/neu positive gastric and
gastroesophageal junction cancer.
CYNK-101 is an investigational genetically engineered natural
killer cell therapy designed to synergize with antibody
therapeutics, the company said.
The Phase 1/2a clinical trial will evaluate safety and
preliminary efficacy.
"Gastric cancer represents the fifth most common cancer
worldwide, and in advanced stages of the disease, continues to be
associated with less than desirable survival outcomes despite
recent advances," said Chief Executive Robert Hariri.
Write to Michael Dabaie at michael.dabaie@wsj.com
(END) Dow Jones Newswires
November 29, 2021 08:43 ET (13:43 GMT)
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