I-Remdesivir

Incazelo emfushane:

Igama le-API Inkomba Umsunguli Idethi yokuphelelwa yisikhathi kwelungelo lobunikazi(e-US)
I-Remdesivir Ama-Antivirus (Ebola, Covid-19) IGileyadi  

 


Imininingwane Yomkhiqizo

Omaka bomkhiqizo

IMINININGWANE YOMKHIQIZO

I-Remdesivir umuthi we-antiviral oqondise uhla lwamagciwane. Yasungulwa ekuqaleni eminyakeni eyishumi edlule ukuze yelaphe i-hepatitis C kanye negciwane elifana nokubanda elibizwa ngokuthi i-respiratory syncytial virus (RSV). I-Remdesivir ibingeyona indlela yokwelapha esebenzayo yanoma yisiphi isifo. Kodwa yabonisa isithembiso ngokumelene namanye amagciwane.

Abacwaningi bahlole i-remdesivir ezivivinyweni zomtholampilo ngesikhathi sokuqubuka kwe-Ebola. Eminye imithi yophenyo yayisebenza kangcono, kodwa kwaboniswa ukuthi iphephile ezigulini. Ucwaningo kumaseli nasezilwaneni luphakamise ukuthi i-remdesivir ibisebenza ngempumelelo ekulweni namagciwane emndenini we-coronavirus, njenge-Middle East Respiratory Syndrome (MERS) kanye ne-Severe Acute Respiratory Syndrome (SARS).

I-Remdesivir isebenza ngokuphazamisa ukukhiqizwa kwegciwane. AmaCoronavirus anezakhi zofuzo ezenziwe i-ribonucleic acid (RNA). I-Remdesivir iphazamisa enye yama-enzyme abalulekile igciwane eliwadingayo ukuze liphindaphinde i-RNA. Lokhu kuvimbela igciwane ukuthi lingaphindaphindeki.

Abaphenyi baqale isivivinyo esingahleliwe, esilawulwayo se-antiviral ngoFebhuwari 2020 ukuze bahlole ukuthi i-remdesivir ingasetshenziswa yini ukwelapha i-SARS-CoV-2, i-coronavirus ebangela i-COVID-19. Ngo-April,imiphumela yokuqalaiveze ukuthi i-remdesivir isheshise ukululama ezigulini ezilaliswe esibhedlela ezine-COVID-19 enzima. Kube umuthi wokuqala ukuthola imvume yokusebenzisa izimo eziphuthumayo kwa-US Food and Drug Administration (FDA) ukwelapha abantu abalaliswe esibhedlela nge-COVID-19.

Abacwaningi manje sebeqedile ukuhlola, okwaziwa nge-Adaptive COVID-19 Treatment Trial (ACTT-1). Lolu cwaningo beluxhaswe yiNational Institute of Allergy and Infectious Diseases (NIAID). Umbiko wokugcina uvele kuI-New England Journal of Medicinengo-Okthoba 8, 2020.

ISItifiketi

2018 GMP-2
原料药GMP证书201811 (captopril,thalidomide njll)
I-GMP-of-PMDA-in-Chanyoo-平成28年08月03日 Nantong-Chanyoo-Pharmatech-Co
I-FDA-EIR-Letter-201901

UKUPHATHWA KWEKHWALITHI

Ukuphathwa kwekhwalithi1

Isiphakamiso18Amaphrojekthi Wokuhlola Ukuvumelana Kwekhwalithi asegunyaziwe4, futhi6amaphrojekthi angaphansi kokugunyazwa.

Ukuphathwa kwekhwalithi2

Uhlelo lokuphatha ikhwalithi yamazwe ngamazwe oluthuthukile lwenze isisekelo esiqinile sokuthengisa.

Ukuphathwa kwekhwalithi3

Ukugadwa kwekhwalithi kusebenza kuwo wonke umjikelezo wempilo womkhiqizo ukuze kuqinisekiswe ikhwalithi nomphumela wokwelapha.

Ukuphathwa kwekhwalithi4

Ithimba Lezindaba Zokulawula Ochwepheshe lisekela izimfuno zekhwalithi ngesikhathi sokufaka isicelo nokubhaliswa.

UKUPHATHWA KOMKHIQIZO

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