Trump Administration Reaches Deal to Manufacture Drugs, Ingredients Needed to Treat COVID-19

The Trump administration is providing $354 million to a company that will head efforts to manufacture key drugs and drug ingredients for use against COVID-19.

Virginia-based Phlow Corporation is heading a team that will provide manufacturing of active pharmaceutical ingredients and the chemical compounds for those ingredients, as well as generic drugs that are in short supply because of surges in hospitalized patients due to the COVID-19 pandemic.

The ingredients and drugs will be manufactured in the United States, including a new facility that will be erected in Virginia. The specific drugs weren’t named but doctors have warned of shortages of hydroxychloroquine because of its widespread use against COVID-19. Hydroxychloroquine is usually used against malaria, lupus, and rheumatoid arthritis.

Shortages of the related chloroquine, the antibiotic azithromycin, and the sedative fentanyl have also seen large increases in use during the pandemic, according to Premier Inc.

The federal government is awarding $354 million to Phlow in a contract that includes an additional $458 million as potential options. Phlow is a start-up founded this year “to help our nation secure its own strategic drug reserve.”

Phlow CEO Dr. Eric Edwards said America needs a reliable source of domestically manufactured pharmaceuticals and key drug ingredients in the midst of the pandemic.

An arrangement of hydroxychloroquine pills in Las Vegas, Nev., on April 6, 2020. (John Locher/AP Photo)

“This advanced manufacturing capability will significantly fortify our nation’s pharmaceutical supply chain for critical medicines, including many required to treat patients hospitalized with COVID-19,” he added in a statement, referring to a disease caused by the CCP (Chinese Communist Party) virus, a novel coronavirus from China.

Rosemary Gibson, a Phlow board member, told The Epoch Times last month that many countries, including the United States, are dependent on China for thousands of medicines.

“If China shut the door on exports of the core chemicals, and other ingredients to make them, we’ll see, the countries waiting in line to get vital medicines to care for their populations. We’re already beginning to see the pricing rivalry for certain drugs that are now becoming more scarce because global demand has increased with coronavirus. It’s a very serious situation that we’re approaching,” she said.

The new project Phlow is heading will be seen in the future “as a defining moment and inflection point for protecting American families—and our country—from current and future public health threats,” Peter Navarro, director of the White House Office of Trade and Manufacturing Policy, said in a statement Tuesday.

The past decades have seen a decline in the manufacturing of generic medicines and drug ingredients in the United States. Over 80 percent of active pharmaceutical ingredients and chemical ingredients used in the United States to manufacture generics and over-the-counter drugs are produced abroad. The majority come from China and India.

Phlow is partnering with Civica Rx, a non-profit pharmaceutical company aimed at bringing down the cost of drugs; the Medicines for All Institute at the Virginia Commonwealth University; and AMPAC Fine Chemicals, a Las Vegas-based manufacturing company that produces active pharmaceutical ingredients. The group has already begun manufacturing chemical ingredients, active ingredients, and finished forms for over a dozen medicines to treat patients hospitalized with COVID-19.

NTD Photo
Researchers at the Microbiology Research Facility work with CCP virus samples as a trial begins to see whether hydroxychloroquine can prevent or reduce the severity of the COVID-19, at the University of Minnesota in Minneapolis, Minnesota, on March 19, 2020. (Craig Lassig/Reuters)

The team is using a technique called “flow” chemistry, or the mixing of chemical reactions in a tube or pipe, which enables faster reactions and other benefits.

“This technology has not been widely adopted in the generic pharmaceutical industry but when used, it can increase the quality, safety, and volume of medicines, yielding lower costs for Americans,” the team said in a press release.

The government funds come from the Biomedical Advanced Research and Development Authority, which is part of the Department of Health and Human Services.

“America has the capabilities, resources, and expertise to secure our medical supply chains; now the Trump Administration is providing the leadership to make it happen,” Health Secretary Alex Azar said in a statement.

“Working with the private sector, HHS is taking a significant step to rebuild our domestic ability to protect ourselves from health threats by utilizing American-made ingredients and creating new American jobs in the process.”

From The Epoch Times