<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="After weeks of polarizing debate over the use of two generic anti-malarial drugs, hydroxychloroquine and chloroquine, the Food and Drug Administration this week warned they were not “safe and effective” when used on COVID-19 patients.” data-reactid=”16″>After weeks of polarizing debate over the use of two generic anti-malarial drugs, hydroxychloroquine and chloroquine, the Food and Drug Administration this week warned they were not “safe and effective” when used on COVID-19 patients.

However, the hydroxychloroquine debate is far from over, as the drug gets qualified support from others deeply involved in the war against the coronavirus, and is used to treat COVID-19 patients in controlled settings.

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="President Donald Trump sparked a furor recently, when he floated hydroxychloroquine as a potential game-changer in the battle against the pathogen, which has sickened over 2.7 million globally — nearly 900,000 in the U.S. alone.” data-reactid=”18″>President Donald Trump sparked a furor recently, when he floated hydroxychloroquine as a potential game-changer in the battle against the pathogen, which has sickened over 2.7 million globally — nearly 900,000 in the U.S. alone.

Yet according to Henry Miller, founding director of the FDA’s Office of Biotechnology and a Senior Fellow at the Pacific Research Institute, Trump’s public advocacy of the treatment — and the FDA’s initial decision to authorize an emergency use order — gave the debate a needlessly political veneer.

“It’s an example of an FDA action that in a sense was unnecessary…probably politically motivated,” Miller told Yahoo Finance in a recent interview. He also blasted the FDA’s emergency use authorization as unnecessary, because the drug is already approved for off-label uses like lupus and rheumatoid arthritis.

Miller charged that much of the discussion surrounding coronavirus treatments has been tainted by “politically motivated happy talk” that is affecting how officials should interpret the data.

“I’m a Republican, but I resent happy talk, I resent misrepresentation and I resent lies,” Miller added.

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="The agency’s guidance issued on Thursday stopped short of banning its use altogether. Instead, the FDA recommended consumers do not use it independently, and said health professionals should their judgement when prescribing it for a coronavirus patient.” data-reactid=”23″>The agency’s guidance issued on Thursday stopped short of banning its use altogether. Instead, the FDA recommended consumers do not use it independently, and said health professionals should their judgement when prescribing it for a coronavirus patient.

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="Trump’s effusiveness was stoked by a couple of inconclusive early studies, one of which was conducted in France. Yet the decision amplified the findings of other studies, including a preliminary report from the Department of Veterans Affairs, that suggest the drug may be more dangerous when used to treat COVID-19 patients.” data-reactid=”24″>Trump’s effusiveness was stoked by a couple of inconclusive early studies, one of which was conducted in France. Yet the decision amplified the findings of other studies, including a preliminary report from the Department of Veterans Affairs, that suggest the drug may be more dangerous when used to treat COVID-19 patients.

“It’s upsetting because there is only anecdotal data, except for the extremely questionable French studies and there are real holes in that,” Miller said, adding the study has “puzzling flaws.”

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="While there haven’t been any reported deaths linked to the French study, there are concerns about toxicity and what the tradeoff of benefits and risks are.” data-reactid=”26″>While there haven’t been any reported deaths linked to the French study, there are concerns about toxicity and what the tradeoff of benefits and risks are.

<h2 class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="A drug with anecdotal promise, and risks” data-reactid=”27″>A drug with anecdotal promise, and risks

The U.S. now has just over 900,000 confirmed cases, and over 50,000 deaths.The U.S. now has just over 900,000 confirmed cases, and over 50,000 deaths.
The U.S. now has just over 900,000 confirmed cases, and over 50,000 deaths.

Despite the debate at the federal level, hydroxychloroquine has some prominent advocates involved in the fight against the pandemic.

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="Recently, Novartis (NVS) CEO Vas Narasimhan told a German newspaper that pre-clinical data in animals and initial clinical studies show the drug actually kills the virus. The drug is produced by Novartis’ Sandoz division as well as Bayer— both of which have donated millions of doses to the national stockpile.” data-reactid=”40″>Recently, Novartis (NVS) CEO Vas Narasimhan told a German newspaper that pre-clinical data in animals and initial clinical studies show the drug actually kills the virus. The drug is produced by Novartis’ Sandoz division as well as Bayer— both of which have donated millions of doses to the national stockpile.

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="Meanwhile, New York state has been allowing the use of hydroxychloroquine in hospitals, anticipating better data as the drug is used in empirical settings. Gov. Andrew Cuomo has cited its anecdotal effectiveness, but said this week that initial studies show its results to be neutral at best.” data-reactid=”41″>Meanwhile, New York state has been allowing the use of hydroxychloroquine in hospitals, anticipating better data as the drug is used in empirical settings. Gov. Andrew Cuomo has cited its anecdotal effectiveness, but said this week that initial studies show its results to be neutral at best.

Dr. Anthony Fauci, the leading White House coronavirus task force member, has previously expressed more caution about using hydroxychloroquine in COVID-19 treatment protocols, saying there has only been “anecdotal evidence,” about its effectiveness.

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="Dr. Ezekiel Emanuel, who served as special advisor for health policy to the director of the White House Office of Management and Budget during the Obama administration echoed those remarks in a recent talk with Yahoo Finance in which he said “we need to rely on data.”” data-reactid=”47″>Dr. Ezekiel Emanuel, who served as special advisor for health policy to the director of the White House Office of Management and Budget during the Obama administration echoed those remarks in a recent talk with Yahoo Finance in which he said “we need to rely on data.”

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="As the public debate ramps up, its sparked increased demand for hydroxychloroquine — something that’s prompted other states — such as Ohio, Texas and Nevada — to protect access for patients who need the drug for off-label uses. Reports of doctors ordering it for themselves, friends and family, have resulted in supply shortages.” data-reactid=”48″>As the public debate ramps up, its sparked increased demand for hydroxychloroquine — something that’s prompted other states — such as Ohio, Texas and Nevada — to protect access for patients who need the drug for off-label uses. Reports of doctors ordering it for themselves, friends and family, have resulted in supply shortages.

Miller, however, hopes the FDA’s rush to validate hydroxychloroquine doesn’t spill over into approvals of other COVID-19 treatments and vaccines in the pipeline.

“I hope that [FDA Commissioner Steven Hahn]… won’t be rushed unnecessarily or inappropriately for insufficient evidence of data,” he said, citing vaccines as a particular worry.

Public officials have cited a timeline of 12 to 18 months for a potential coronavirus cure. However, Miller blasted that as “politically motivated happy talk” and “off by a factor of two, at least.” Fauci is among those who have floated that optimistic time frame, given the urgency of the crisis.

Yet Miller stated that “Fauci has qualified it in a clever way. He says a vaccine that you make and start testing in a year is not a vaccine that is deployable. You can have a candidate, but can’t complete all required testing in a year.”

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="Anjalee Khemlani is a&nbsp;reporter&nbsp;at Yahoo Finance. Follow her on Twitter:&nbsp;@AnjKhem” data-reactid=”53″>Anjalee Khemlani is a reporter at Yahoo Finance. Follow her on Twitter: @AnjKhem

<p class="canvas-atom canvas-text Mb(1.0em) Mb(0)–sm Mt(0.8em)–sm" type="text" content="Read the latest financial and business news from Yahoo Finance” data-reactid=”54″>Read the latest financial and business news from Yahoo Finance

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