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Patients Rush to Virus Test Studies    04/06 06:09

   (AP) -- The new coronavirus made Dr. Jag Singh a patient at his own 
hospital. His alarm grew as he saw an X-ray of his pneumonia-choked lungs and 
colleagues asked his wishes about life support while wheeling him into 
Massachusetts General's intensive care unit.

   When they offered him a chance to help test remdesivir, an experimental drug 
that's shown promise against some other coronaviruses, "it did not even cross 
my mind once to say 'no,'" said Singh, a heart specialist. 

   Coronavirus patients around the world have been rushing to join remdesivir 
studies that opened in hospitals in the last few weeks.

   Interest has been so great that the U.S. National Institutes of Health is 
expanding its study, which has nearly reached its initial goal of 440 patients. 
The drug's maker, California-based Gilead Sciences, is quickly ramping up its 
own studies, too.

   "I would enroll my family in a heartbeat" if the need arose, said Dr. Libby 
Hohmann, who placed Singh and nearly 30 others in the NIH one at Mass General. 
To have no approved medicines for COVID-19 now is "kind of terrifying," she 

   For most people, the new coronavirus causes mild or moderate symptoms, which 
can include fever and cough but sometimes pneumonia requiring hospitalization. 
The risk of death is greater for older adults and people with other health 

   Remdesivir is given through an IV. It's designed to interfere with an enzyme 
that reproduces viral genetic material. 

   In animal tests against SARS and MERS, diseases caused by similar 
coronaviruses, the drug helped prevent infection and reduced the severity of 
symptoms when given early enough in the course of illness. It's farther along 
in testing than many other potential therapies and the current studies could 
lead to regulatory approval.

   Gilead has given remdesivir to more than 1,700 patients on a case-by-case 
emergency basis, but more people ultimately will be helped if the company does 
the needed studies to prove safety and effectiveness, chief executive Dan O'Day 
wrote in a recent letter to the public. 

   "Many people have reached out to Gilead to advocate for access to remdesivir 
on behalf of friends and loved ones. I can only imagine how it must feel to be 
in that situation," he wrote. "We are taking the ethical, responsible approach."

   In another letter on Saturday, O'Day said the company has 1.5 million doses, 
which could mean more than 140,000 treatment courses, depending on how long 
treatment needs to last. The company is providing the drug for free for now and 
has set a goal of making 500,000 treatment courses by October and more than a 
million by the end of the year. 

   Gilead supplied remdesivir for two studies in China expected to give results 
by the end of the month. It also launched two studies for hospitalized patients 
in the U.S., Asia, Europe and elsewhere. One in severely ill patients tests 
five versus 10 days of treatment. Another in moderately sick patients compares 
those two options to standard care alone. 

   "There's so much anxiety about the disease that the patients are quite 
interested" and no one offered the chance has refused, said Dr. Arun Sanyal, 
the study leader at Virginia Commonwealth University in Richmond.

   The first patient he enrolled was a previously healthy middle-aged man who 
had an out-of-state visitor a few days before his symptoms began. What started 
as mild illness escalated to profound shortness of breath requiring 
supplemental oxygen.

   At University Hospitals Cleveland Medical Center, Dr. Grace McComsey has 
enrolled roughly half a dozen patients.

   "We're seeing more and more younger people, like 30, really sick," she said.

   The NIH study is the most rigorous test. It compares remdesivir to placebo 
infusions, and neither patients nor doctors know who is getting what until the 
end of the study. Besides the U.S., it's open in Japan, Korea and Singapore.

   In Chicago, an 89-year-old man was Northwestern Memorial Hospital's first 
participant and "the family was very excited" to have him included, said 
infectious diseases chief Dr. Babafemi Taiwo.

   At the University of California, Irvine, Dr. Alpesh Amin has enrolled 
several patients. All are getting standard care even if they wind up getting a 
placebo rather than remdesivir, Amin said.

   The Boston cardiologist, Singh, said he was willing to take that chance to 
advance science even if he personally winds up not benefiting. He's now 
recovering at home after spending a week in the hospital.

   "The word 'placebo' freaks some people out," but rigorous testing is needed 
to avoid giving false hope or using something unsafe. Still, it's tough to face 
patients with no proven therapy now, Hohmann said.

   "The worst thing is seeing some really young people who are really, really 
sick," such as a 49-year-old man with three young children on life support, she 
said. "That's pretty awful."


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