Novartis receives FDA nod for malaria drug trial on COVID-19 patients
Category: #health  By Mateen Dalal  Date: 2020-04-21
  • shareshare_icon
  • Twitter
  • Facebook
  • LinkedIn

Novartis receives FDA nod for malaria drug trial on COVID-19 patients

Novartis has received approval from the U.S. Food and Drug Administration for clinical trials to study the efficacy of hydroxychloroquine, which is essentially a drug for malaria, for the treatment of hospitalized patients suffering from COVID-19. The trial has nearly 440 patients and is expected to be conducted at over a dozen locations all across the U.S.

Apparently, the FDA has issued an authorization for emergency use to let the doctors use the drug on patients with COVID-19 under particular conditions. However, there has been no availability of any official product that has been approved by the FDA in order to treat coronavirus.

U.S. President, Trump has consistently supported hydroxychloroquine as a drug that can prove to be a game-changer across the battle against the new coronavirus. An international poll held recently, that had over 6,200 doctors, found out that the drug was the most effective way to treat COVID-19 out of a list having over a dozen options.

There have been several experts from the health field who have warned against the impulsive decision regarding the drug and have also cautioned against the potential side effects. A recent study on chloroquine in Brazil, a similar drug, had been halted in a group of patients early after it was noticed that some had developed heart rhythm issues.

The Chief Medical Officer and Global Drug Development at Novartis, John Tsai commented that the company identifies the importance of giving answers to the scientific questions demanding if hydroxychloroquine will benefit the patients suffering from COVID-19.  The company mobilized immediately to be able to address the question in a double-blind, placebo-controlled and randomized study.

Various firms such as Roche, Gilead Sciences and Novartis have been testing older medicines that were originally developed to treat various other diseases, looking for any signs that they could be repurposed to fight coronavirus pandemic. Gilead has expanded its trial for Ebola drug remdesivir.

 

Source Credit- https://www.washingtontimes.com/news/2020/apr/20/novartis-wins-approval-fda-start-hydroxychloroquin/

 

 

  • shareshare_icon
  • Twitter
  • Facebook
  • LinkedIn


About Author

Mateen Dalal     twitter

Mateen Dalal

A qualified electronics and telecommunication engineer, Mateen Dalal embarked on his professional journey working as a quality and test engineer. Harnessing his passion for content creation however, Mateen pens down industry-rich articles for ReportsGO.com and a few o...

Read More..

More News By Mateen Dalal

General Motors to recoup USD 1.9 Bn from LG spent on Bolt EV recall

General Motors to recoup USD 1.9 Bn from LG spent on Bolt EV recall

By Mateen Dalal

GM will recover almost all the costs from the recall of its Bolt EV models. Despite the EV battery manufacturing mishap from LG, the two companies will continue to work together. General Motors (GM) has agreed to recover around USD 1.9 billion f...

Tata Motors records 25% jump in global sales in second quarter of 2021

Tata Motors records 25% jump in global sales in second quarter of 2021

By Mateen Dalal

The automaker’s annual wholesale growth has been around 24%. The company saw a 10% rise in passenger car sales during Q2 2021, as compared to the same period in 2020. Tata Motors Limited reported substantial growth in Q2 2021, with its glo...

Carbon Budgets for corporate business travels to hit airlines: Report

Carbon Budgets for corporate business travels to hit airlines: Report

By Mateen Dalal

With major companies considering ways to reduce carbon emissions from corporate travel, airlines are preparing for a setback in business-class travel, which is an important revenue driver according to industry experts and executives. The airline ind...