Trial using Regeneron’s antibody drug – which was given to Trump – to treat severely ill COVID-19 patients paused over ‘potential safety concern’
- Outside monitors have advised Regeneron to pause its test of its coronavirus antibody drug in hospitalized patients, the company said Friday
- Regeneron cited a ‘potential safety concern’ but did not give any specifics
- Its trials of the antibody cocktail – which was given to President Trump – to treat less severely ill patients can continue
- Competitor Eli Lilly had to pause its trial of its antibody therapy in severely ill COVID-19 patients earlier this month
Regeneron’s highly-anticipated coronavirus antibody drug faced a setback Friday when an outside panel recommended its trial of the antibody cocktail to treat severely-ill COVID-19 patients be paused over a ‘potential safety concern.’
Trials for the antibody cocktail – the same experimental treatment given to President Trump shortly after he tested positive for COVID-19 earlier this month – to treat coronavirus patients with milder illness can continue, however.
It’s the second antibody drug trial paused in the span of a couple of weeks. Eli Lilly’s trial of its antibody treatment, combined with remdesivir, to treat hospitalized was also paused on October 13.
Regulators say that trial pauses are to be expected, even characterizing them as encouraging signs that the process of testing drugs is and vaccines is working as it should be flagging safety concerns ahead of approvals.
Nonetheless it’s a blow to President Trump, who has been pushing for the approval of therapeutics to be approved by Election Day since changes to the Food and Drug Administration’s (FDA) requirements for authorizing coronavirus vaccines thwarted his hopes of having a vaccine by November 3.
Trials for Regeneron’s coronavirus antibody drug (pictured) to treat hospitalized COVID-19 patients have been paused over a ‘potential safety concern,’ the firm said Friday (file)
Regeneron said Friday that independent monitors had recommended placing on hold enrollment of the most severely ill patients – those who need intense oxygen treatment or breathing machines – because of a potential safety problem and unfavorable balance of risks and benefits.
Neither the company nor its safety monitors have offered any specifics on the nature of the ‘safety concern.’
The study can continue to test the two-antibody drug combo in hospitalized patients who need little or no extra oxygen, the monitors said. Other studies in mild or moderately ill people also are continuing.
Antibodies are proteins the body makes when an infection occurs; they attach to a virus and help it be eliminated.
But it can take several weeks for the most effective ones to form. The experimental drugs aim to help immediately, by supplying concentrated versions of one or two antibodies that worked best against the coronavirus in lab and animal tests.
Earlier this month, a different group of monitors recommended pausing enrollment in a U.S. National Institutes of Health (NIH) study testing an Eli Lilly antibody drug to investigate a possible safety issue in hospitalized patients.
On Monday, the NIH said no safety problem had been verified, but they stopped the study because the drug didn’t seem to work in that situation.
‘These kinds of results are informing us about the timing of the benefit,’ said Dr. Myron Cohen, a University of North Carolina virologist who advises the government on COVID-19 treatments.
Tests in animals suggest that antibody drugs work best when given early in infection to lower the amount of virus, he said. Once someone is very sick, the drugs may not help, but it’s too soon to know if that’s the case, he said.
Doctors already know that timing can matter when it comes to COVID-19 treatments.
Studies suggest that dexamethasone and other steroids can lower the risk of death when given to very sick patients to tamp down an over-active immune system, but they may be harmful for those who are only mildly ill.
Lilly and Regeneron have asked the Food and Drug Administration to allow emergency use of their experimental antibody drugs for mild and moderately ill patients who don´t need hospitalization.
Regeneron said it would share Friday’s advice from independent monitors with the FDA and leaders of a separate study in the United Kingdom testing its drug in hospitalized patients.
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