Remdesivir therapy, an fresh antiviral therapy that has been utilized to treat COVID-19 , has no considerable effect on a patient’s likelihood of survival, a study from the World Health Organization (WHO) has found.

The antiviral medication, produced by U. S. drugmaker Gilead Sciences , was one of several drugs used to treat Chief executive Donald Trump following their CCP (Chinese Communist Party) virus diagnosis earlier this particular month. It is among the first for use as a treatment for COVID-19, the disease caused by the virus.

WHO’s highly expected “Solidarity” trial examined the consequences of remdesivir and three additional potential drug regimens, which includes hydroxychloroquine , anti-HIV drug mixture lopinavir/ritonavir, and interferon, within 11, 266 adult individuals across more than 30 nations.

It discovered that the four regimens “appeared to have little or no effect on hospitalized” or reduce the duration associated with hospital stay or the have to ventilate patients.

“These Remdesivir, Hydroxychloroquine, Lopinavir and Interferon regimens seemed to have little effect on in-hospital mortality, ” the study discovered.

The WHO ALSO mentioned Thursday that will its study also found that every one of the treatments appeared to have got little or no effect on 28-day fatality or the length patients continued to be hospitalized. The study is however to be peer-reviewed.

Remdesivir was first developed like a treatment for Ebola, plus works by disrupting the virus’ ability to replicate.

“We are aware that preliminary data from the World Wellness Organization’s (WHO) SOLIDARITY Test has been made public prior to syndication in a peer-reviewed journal, ” Gilead told the Economic Times in a statement.

“The emerging information appear inconsistent with more powerful evidence from multiple randomized, controlled studies validating the particular clinical benefit of remdesivir.

“We are concerned the information from this open-label global test has not undergone the thorough review required to allow for helpful scientific discussion, particularly provided the limitations of the test design. ”

Daniel O’Day, Chairman & CEO of Gilead Sciences, said in an open letter upon Oct. 8 that according to a placebo-controlled Phase 3 study brought by the U. S Nationwide Institute of Allergy plus Infectious Diseases (NIAID) that will covered approximately 1, 060 hospitalized patients worldwide, sufferers receiving remdesivir recovered 5 days faster on average, and patients with severe illness, seven days faster.

Daniel O' Day

Daniel O' Day

Daniel O’Day, TOP DOG of Gillead Sciences Incorporation., speaks during a meeting with Leader Donald Trump in the Oblong Office of the White Home in Washington, on Might 1, 2020. (Jim Watson/AFP via Getty Images)

The treatment also reduced the possibilities of patients progressing to more serious stages of the disease exactly where they would require new or even additional oxygen support, the research found, said O’Day.

“In the largest number of patients in the study, those people on low-flow oxygen, there is a significant reduction in mortality within a post-hoc analysis. In the general population, the results showed the trend in mortality decrease, ” he added.

The WHO failed to immediately respond to a demand by The Epoch Times designed for comment.

Upon May 1, remdesivir had been granted emergency use consent by the Food and Drug Management, and its use has given that been approved or certified to treat COVID-19 in more than fifty countries worldwide .

The president started remdesivir therapy on April. 2, shortly after his COVID-19 diagnosis. White House doctor Dr . Sean Conley mentioned in a memorandum at the time that this experimental antiviral therapy has been chosen “in consultation along with specialists. ”

The president also acknowledged an experimental antibody beverage treatment from  Regeneron Pharmaceutical drugs Inc. for his recuperation.   Trump was able to get the treatment through a “compassionate use” exemption.

Regeneron’s polyclonal anti-viral antibody beverage includes a collection of antibodies made by B cells. The protection and effectiveness of the medication have not yet been set up through clinical trials.

Mimi Nguyen Ly and Reuters led to this report.