SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Strategies & Market Trends : 2026 TeoTwawKi ... 2032 Darkest Interregnum
GLD 414.48+0.7%Jan 9 4:00 PM EST

 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext  
From: Julius Wong3/18/2022 3:12:39 PM
  Read Replies (3) of 219185
 
Ivermectin had no clinical benefit against COVID-19 in largest study to date - WSJ

Mar. 18, 2022 11:18 AM ET Merck & Co., Inc. (MRK), PFE By: Dulan Lokuwithana, SA News Editor 259 Comments

RafaPress/iStock via Getty Images

A group of researchers evaluating the effect of repurposed drugs against COVID-19 found that oral antiparasitic medication ivermectin did not improve patient outcomes in the largest trial of its kind to date, The Wall Street Journal reported on Friday.

Ivermectin marketed by Merck (NYSE: MRK) as Stromectol for parasitic infestations sparked controversy during the pandemic prompting the U.S. Food and Drug Administration (FDA) to issue warnings against its excessive use.

“There was no indication that ivermectin is clinically useful,” said Edward Mills, a lead investigator of the trial and a professor of health sciences at Canada’s McMaster University in Hamilton, Ontario.

The findings have been accepted for publication in a major peer-reviewed medical journal, and on Friday, Dr. Mills is scheduled to present the data at an event sponsored by the National Institutes of Health.

The latest trial conducted in Brazil involved 1,358 adults with COVID-19 symptoms. All study participants were at risk of developing the severe form of the disease with a history of pre-existing conditions such as diabetes, hypertension, cardiovascular disease, or lung disease. Half of them received Ivermectin pills for three days, and the other half received a placebo.

Dr. Mills and the team looked at their hospitalizations rates within 28 days. In addition, they gathered data on how fast the patients cleared the virus, how soon their symptoms improved, whether they were in hospital or were relying on ventilators for less time, and the differences in death rates.

For accuracy, they analyzed data in three different ways, and in each scenario, ivermectin was found to have no impact on the improvement of patient outcomes.

Last year, the FDA authorized oral COVID-19 pills, Paxlovid and molnupiravir, developed by Pfizer (NYSE: PFE) and Merck (MRK)/ Ridgeback Biotherapeutics LP, respectively, for at-home use.
Report TOU ViolationShare This Post
 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext