FDA Approves Clinical Trials for South Korean COVID-19 Drug Candidate

The South Korean biopharmaceutical company Genexine Inc. announced on Thursday that it has obtained authorization in the United States to conduct clinical trials for its potential COVID-19 drug.
Clinical trials of the cancer drug GX-17, in the experimental phase for the treatment of COVID-19 patients, have been authorized by the Food and Drug Administration (FDA).
Jointly developed by the US-based biopharmaceutical company NeoImmuneTech Inc, GX-17 will be administered to adult COVID-19 patients with moderate symptoms, the company said.
GX-17 is an immunotherapy drug that targets interleukin-7, whose role is essential in the proliferation of T cells in the body.
Genexine is a member of a consortium of six companies, including SK Life Science Inc., a subsidiary of the country’s third-largest conglomerate SK, to develop new COVID-19 vaccines.
The consortium has successfully tested its vaccine on monkeys. Binex, a member of the consortium, has completed the production of a sample.
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