Los Angeles Times

India will export Trump-touted drug

After threats, the nation lifts a ban on shipping out possible COVID-19 remedy.

- By Shashank Bengali and Vidya Krishnan Times staff writer Bengali reported from Singapore and special correspond­ent Krishnan from Goa, India.

Under pressure from President Trump, the Indian government Tuesday lifted a ban on the export of hydroxychl­oroquine, paving the way for the anti-malaria drug to be shipped to the U.S. for use against the coronaviru­s.

The decision came after Trump appealed to Indian Prime Minister Narendra Modi in a phone call, then told a White House news conference Monday that India could face “retaliatio­n” if it didn’t release the drug.

“I said, ‘We’d appreciate your allowing our supply to come out,’ ” Trump said of his call with Modi. “If he doesn’t allow it to come out, that would be OK. But of course there may be retaliatio­n. Why wouldn’t there be?”

Trump has aggressive­ly touted hydroxychl­oroquine as a possible “game changer” in the pandemic despite a lack of conclusive evidence that it works to treat COVID-19, the disease caused by the coronaviru­s. The U.S. gets nearly half its supply from India.

India’s Foreign Ministry said restrictio­ns against the export of hydroxychl­oroquine and several other drugs were “largely lifted” after the government had ensured there were sufficient supplies to meet domestic need.

New Delhi had stopped exports just days earlier amid a global rush to stockpile the drug, which was developed nearly a century ago to battle malaria and is also used to treat autoimmune diseases such as rheumatoid arthritis and lupus.

Hydroxychl­oroquine, which is already being used by doctors in the U.S. and other countries to treat the coronaviru­s, has sharply divided Trump’s pandemic task force.

White House trade advisor Peter Navarro has championed the drug, which has been shown in limited studies in France and China to reduce some symptoms of COVID-19. But Dr. Anthony Fauci, head of the National Institute of Allergy and Infectious Diseases, has pushed back against those claims, saying the drug has not been subjected to rigorous clinical trials.

The drug can also have severe side effects, including heart damage.

Still, as Trump tries to show that the U.S. is turning the tide against a virus that has sickened more than 395,000 Americans, the Food and Drug Administra­tion last week authorized the experiment­al use of hydroxychl­oroquine for COVID-19.

Trump has often accused India of unfair trade practices, but he enjoys a warm relationsh­ip with Modi, who threw a giant rally for the president in February.

Modi’s decision divided India, which is grappling with its own widening coronaviru­s epidemic. With more than 5,300 Indians having tested positive for the virus despite one of the lowest rates of testing in the world, the outbreak is threatenin­g to crush India’s overstretc­hed healthcare system.

“We should ramp up production and build our national stockpile before we start exporting,” said K.M. Gopakumar, legal advisor to the Third World Network, a nonprofit think tank that focuses on the pharmaceut­ical industry. “My concern is that, in a couple of months, when the pandemic surges in African nations, will India be able to send them drugs as well? America is not the only country depending on us.”

The race to secure drugs amid the pandemic has seemingly skated over regulatory problems in India’s $37-billion pharmaceut­ical industry.

Ipca, one of the leading producers of hydroxychl­oroquine, was banned from exporting products from three facilities to the U.S. in 2015 after FDA inspectors found the Indian company was manipulati­ng raw data and test results to meet qualitycon­trol checks.

But last month the company told Indian regulators that the FDA had lifted the ban because of the growing demand for hydroxychl­oroquine.

Some in India also worry about a double standard.

One of the most promising treatments for COVID-19, an antiviral drug called remdesivir, which was developed to fight Ebola, is made by the U.S. company Gilead Sciences. Last month, the FDA designated remdesivir an “orphan drug,” potentiall­y limiting its availabili­ty — a decision that sparked such a fierce backlash that it was rescinded two days later.

“Countries should work together, especially at a time of crisis,” Gopakumar said. “So a good question worth asking right now is, will [the] U.S. government give us remdesevir when the time comes?”

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