Home World Wide News Trump admin’s botched pandemic response detailed in whistleblower complaint

Trump admin’s botched pandemic response detailed in whistleblower complaint

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Trump admin’s botched pandemic response detailed in whistleblower complaint

Closeup photograph of a coach's whistle on a blue background.

A new whistleblower complaint by a former US health official details how the Trump administration’s COVID-19 response was hampered by cronyism and denial about the virus’s severity. The 89-page complaint filed by Rick Bright, an immunology expert who led the Biomedical Advanced Research and Development Authority (BARDA) until he says he was forced out of his position, provides an inside look at the Trump administration’s approach to public health before and during the pandemic.

From spring 2017 until his “involuntary removal” last month, “HHS [Health and Human Services] leadership pressured Dr. Bright and BARDA to ignore expert recommendations and instead to award lucrative contracts based on political connections and cronyism,” the complaint said. “Dr. Bright repeatedly clashed with [Assistant Secretary for Preparedness and Response Robert] Kadlec and other HHS leaders about the outsized role played by John Clerici, an industry consultant to pharmaceutical companies with a longstanding connection to Dr. Kadlec, in the award of government contracts.”

For example, Bright in 2017 objected to a push “to extend a contract with Mr. Clerici’s client, Aeolus Pharmaceuticals, which an IPR [in-process review] had concluded should be allowed to expire without further funding. In attempting to justify the extension of this failed contract, Mr. Clerici emphasized that Aeolus’s Chief Executive Officer was a ‘wildcard’ and a friend of Jared Kushner, President Trump’s son-in-law and a Senior Advisor to the President. Dr. Bright stood his ground on this contract, which led to some discord between him and HHS leadership.”

In fall 2019, Bright says he “rejected pressure by Dr. Kadlec to invest millions of dollars in EIDD-2801, a drug developed at Emory University by a longtime friend of Dr. Kadlec. EIDD-2081 was presented as a ‘miracle cure’ for influenza, Ebola and nearly every other virus, even though the developer had not yet conducted clinical trials and no data had been compiled to demonstrate either the efficacy or safety of the drug in humans.”

Rick Bright.

In February 2020, EIDD-2801 makers “were once again seeking funding for the drug—this time, as a treatment for COVID-19.” Bright says he fought the request for $100 million in part because “Emory still had not completed the clinical trials for which it had received nearly $30 million in NIH and DOD funds.” Ultimately, “the award was not made prior to Dr. Bright’s departure from BARDA.”

In a statement to The New York Times, Clerici said he “unequivocally” denied any wrongdoing and that “it’s sad that during a pandemic, Dr. Bright and his team have chosen to distract people like Dr. Kadlec, who are critical to the response, with politically motivated allegations. The record is clear that his allegations are false and will be proven so.”

Trump’s push for chloroquine

Bright’s whistleblower complaint, which cites many internal emails and events from in-person meetings, was filed with the US Office of Special Counsel. Among other things, the complaint delves into the curious case of hydroxychloroquine, a malaria drug President Donald Trump repeatedly promoted as a coronavirus treatment despite a lack of evidence. (The FDA has since issued a warning about the drug, saying it “should be limited to clinical trial settings or for treating certain hospitalized patients.”)

“In an apparent effort to score a short-term political victory for the Administration during the escalating health crisis, the Office of the ASPR [Assistant Secretary for Preparedness and Response] pressured BARDA to promote the malaria drug chloroquine as a therapeutic for COVID-19, despite a clear lack of scientific support,” the whistleblower complaint said.

Bright and another concerned colleague brokered a compromise in which the drug would remain “in the hands of healthcare professionals, and out of the hands of the public,” ensuring that “the drugs were administered to patients only under close physician supervision and who were known to be infected with the virus.”

“Despite the brokered compromise, the Administration nevertheless continued to push for expanded, unsupervised access to chloroquine and hydroxychloroquine, in blatant violation of the EUA [Emergency Use Authorization] issued by its own FDA and regardless of the risk to the American public,” the complaint said.

Bright’s complaint continued:

On April 4, 2020, hours after President Trump once again touted hydroxychloroquine as a treatment for COVID-19 during a White House press conference, HHS Assistant Secretary for Health Adm. Brett Giroir, M.D., instructed FEMA Administrator Peter Gaynor, Vice Director for Logistics of the Joint Chiefs of Staff Rear Adm. John Polowczyk, and Dr. Kadlec to mobilize the nation’s supply chain to “flood NY and NJ with treatment courses [of hydroxychloroquine].” Admiral Giroir issued this instruction based on orders from the White House. Mr. Gaynor likewise had received instructions from FDA Commissioner Dr. Stephen Hahn to distribute hydroxychloroquine to pharmacies nationwide, even though the EUA did not provide for outpatient use of the drug.

HHS announced its acceptance of a donation of 3 million hydroxychloroquine pills from Bayer, and the drug was “imported from factories in Pakistan and India that had not been inspected by the FDA,” the complaint said.

Bright revealed details to journalist

Bright eventually concluded that “he had exhausted all avenues to alert government officials, who refused to listen or take appropriate action to accurately inform the public” and that “his only remaining avenue was to share his concerns with a journalist who had contacted him and understood the specific issue and risks associated with these drugs and who had already gathered substantial information from multiple sources.”

Bright “provided information to a reporter about the specific danger to the public health and safety caused by the Administration’s decision to release these untested drugs for use by the general public,” the complaint said. The journalist was Katherine Eban, whose Reuters article on April 16 revealed internal emails about the Trump administration’s chloroquine push.

“HHS leadership, including [HHS] Secretary [Alex] Azar and Dr. Kadlec, were already gunning for Dr. Bright’s removal because of other issues he had raised about fraud, waste, and abuse, but they chose to remove him as BARDA Director within days of publication of the article about chloroquine because they suspected that he was the source,” Bright’s complaint said.

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