摘要:
The present invention relates to a solid composition comprising amorphous sofosbuvir and amorphous daclatasvir and to a process for the preparation of the solid composition. The pre- sent invention further relates to a pharmaceutically acceptable composition comprising the solid composition. Yet further, the present invention relates the use of the solid composition and the pharmaceutically acceptable composition comprising the solid composition for use in the treatment of hepatitis C.
摘要:
The invention pertains to the use of soluble sodium in the manufacture of a composition or kit of parts for (therapeutically) improving and prolonging blood plasma uridine levels and tissue availability of uridine, and/or for treating or preventing impaired blood plasma uridine levels and tissue availability of uridine, and/or for preventing/treating disorders associated with impaired blood plasma and tissue availability of uridine, in a mammal, preferably a human being, by orally co-administering soluble sodium and uridine in a molar ratio of soluble sodium to uridine of more than 1 : 1, preferably more than 1.5: 1, more preferably more than 2: 1, even more preferably at least 2.5: 1, even more preferably at least 2.8: 1, more preferably 3 : 1 - 15: 1, most preferably 3 : 1 - 10: 1, particularly 3 : 1 - 5: 1.
摘要:
In some aspects, the present disclosure provides compounds of the formula: Formula (I) wherein the variables are defined herein are provided, which may be used to inhibit viral replication. In some embodiments, these compounds may be used to treat an infection of hepatitis B virus.
摘要:
Provided herein are methods of treating long-chain fatty acid disorders, conditions, such as rhabdomyolysis, associated with inflammation and/or long-chain fatty acid disorders, and inflammation associated with long-chain fatty acid disorders.
摘要:
The present invention features compounds effective in inhibiting active against Hepatitis C virus ("HCV") polymerase. The invention also features processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.
摘要:
The present invention features compounds effective in inhibiting active against Hepatitis C virus ("HCV") polymerase. The invention also features processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.