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  • Celltrion announced results of external clinical trials
  • by Lee, Tak-Sun | translator Choi HeeYoung | Jan 18, 2021 06:13am
for COVID-19 tx on the 18th
The MFDS holds a verification advisory group meeting to evaluate the suitability of clinical trials on the 18th
Final Conditional Marketing Authorization (CMA) decision
The MFDS will hold a verification advisory group meeting on the 17th to evaluate the appropriateness of the clinical trial results for COVID-19 treatment Rekirona developed by Celltrion. And it plans to announce the results on the 18th.

After the verification advisory group meeting, the Central Pharmaceutical Affairs Review Committee and the final review committee decide whether to grant CMA through internal and external verification.

The MFDS is currently operating the Central Pharmacy Review Committee on matters related to the safety and effectiveness of new drugs in accordance with the Pharmaceutical Affairs Law and is undergoing a procedure to seek advice.

Taking into account the severe situation of COVID
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