Recently, according to the relevant provisions of the Drug Administration Law, the State Food and Drug Administration carried out emergency review and approval in accordance with the special approval procedure for drugs, and conditionally approved the combined packaging of the Class 1 innovative drug Xiannuotevir Tablets/Litonavir Tablets (trade name: Xiannuoxin) The first class innovative drug, Remivvir deuterium hydrobromide tablets (trade name: Mindwell), declared by Shanghai Wangshi Biomedical Technology Co., Ltd. was listed.
The above two drugs are oral small molecule neocoronavirus infection treatment drugs, which are used to treat adult patients with mild to moderate neocoronavirus infection. Patients should use drugs strictly according to the instructions under the guidance of doctors. The State Food and Drug Administration requires the holder of the marketing license to continue the relevant research work, complete the conditional requirements within a time limit, and submit the follow-up research results in a timely manner.
Beijing Municipal Medical Insurance Bureau publicized the initial offer for the combined packaging of Xianotevir Tablets/Litonavir Tablets: 750/box.
Xiannuoxin oral small molecule anti COVID-19 innovative drug uses 3CL protease as the target to inhibit viral replication, and Mindevi oral nucleoside antiviral drug inhibits the activity of viral RNA polymerase to block viral replication. Xiannuoxin: accelerate the recovery of symptoms and shorten the course of disease. The antiviral effect is remarkable, and the time of nucleic acid turning negative is shortened. Mindwell: Compared with the PAXLOVIDVV116 group, the clinical recovery time is shorter, and there are fewer concerns about safety.
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