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Senhwa Biosciences, Inc. announced that their first patient has been successfully dosed in Taiwan Phase II Study of Silmitasertib in Hospitalized Adults with COVID-19.

Senhwa Biosciences, Inc. announced that Taiwan Food and Drug Administration has approved its Phase II IND application of Silmitasertib to treat patients with community-acquired pneumonia caused by viral infection.

Senhwa Biosciences, Inc. announced that U.S. Food and Drug Administration has approved its Phase II IND application of Silmitasertib to treat patients with community-acquired pneumonia caused by viral infection.

Senhwa Biosciences, Inc. (TPEx: 6492) announced today that it has submitted an Investigational New Drug (IND) application to U.S. Food and Drug Administration to evaluate its investigational drug, Silmitasertib(CX-4945), for treating patients with community-acquired pneumonia (CAP) caused by viral infection.

Senhwa Biosciences, Inc. announced today that Taiwan FDA has approved its Phase II IND application of Silmitasertib(CX-4945) to treat hospitalized patients with moderate to severe COVID-1.

Senhwa Biosciences, Inc. announced that their first in class new drug Pidnarulex (CX-5461) has been successfully selected to the anticancer pipeline of NIH-sponsored NExT Program (NCI Experimental Therapeutics Program), which will foster the exploration of its therapeutic potential in unmet medical needs and advancement to market.

Senhwa Biosciences, Inc. announced today that their first patient has been successfully dosed, in a phase I clinical study evaluating the combined treatment with Senhwa’s Pidnarulex.