Medicine & TechnologyA study recently showed that treatment for COVID-19 derived from a rare sea animal and historically used for cancer treatment is more efficient by 27.5 times than the popular COVID-19 drug remdesivir.
The results from WHO's Solidarity trial revealed that remdesivir has little to no effect on cutting the hospital days and mortality of COVID-19 patients.
Pharmaceutical giant Pfizer has signed a multi-year deal with Gilead Sciences Inc., to boost the production of its investigational antiviral remdesivir, a potential drug against COVID-19.
The price for remdesivir is out, and Gilead Sciences says it could cost up to $2,340 per patient for most wealthy nations. Some patient advocates contend that the price should be less, considering its development and trials received aid from the U.S. government. Click the link above to learn more.
Gilead's drug for coronavirus, remdesivir, once again shows its potential after a clinical trial reveals that it prevents lung damage in monkeys. Additionally, the results of the trial showed that the monkeys had minimal damage to their lungs in comparison with the control group.
Gilead Sciences just finished its phase 3 trials for remdesivir, and the results have been positive. As for the next step, the company seeks to explore making inhaled versions of the drug for early treatment of COVID-19 as well as easier treatment at home.
The trials for Gilead's remdesivir is said to end in May. With the drug only being used for COVID-19 patients under the emergency use authorization, many worry about their access to the drug that has proved to be helpful against the coronavirus. Click the link above to learn more.
Remdesivir is now finally the first drug to be approved by the US FDA to treat COVID-19. However, controversy has started regarding its price. Experts say that is could cost up to $4,500 despite requiring just $9.32 to make. Click the link to read more.
Remdesivir, the drug candidate of Gilead Sciences showed promising results from its two phase three trials. Experts believe the drug would most likely lead to fast approvals by the Food and Drug Administration as long as proven safe and effective.