Showing posts with label Drug. Show all posts
Showing posts with label Drug. Show all posts

Tuesday, May 19, 2020

Scientists in China believe new drug can stop pandemic 'without vaccine'


A Chinese laboratory has been developing a drug it believes has the power to bring the coronavirus pandemic to a halt.

The outbreak first emerged in China late last year before spreading across the world, prompting an international race to find treatments and vaccines.

A drug being tested by scientists at China's prestigious Peking University could not only shorten the recovery time for those infected, but even offer short-term immunity from the virus, researchers say.

Sunney Xie, director of the university's Beijing Advanced Innovation Center for Genomics, told AFP that the drug has been successful at the animal testing stage.

"When we injected neutralising antibodies into infected mice, after five days the viral load was reduced by a factor of 2,500," said Xie.


"That means this potential drug has (a) therapeutic effect."

The drug uses neutralising antibodies -- produced by the human immune system to prevent the virus infecting cells -- which Xie's team isolated from the blood of 60 recovered patients.

A study on the team's research, published Sunday in the scientific journal Cell, suggests that using the antibodies provides a potential "cure" for the disease and shortens recovery time.

Xie said his team had been working "day and night" searching for the antibody.

"Our expertise is single-cell genomics rather than immunology or virology. When we realised that the single-cell genomic approach can effectively find the neutralising antibody we were thrilled."

He said he hopes that the drug will be ready for use later this year and in time for any potential winter outbreak of the virus, which has infected 4.8 million people around the world and killed more than 315,000.

"Planning for the clinical trial is underway," said Xie, adding it will be carried out in Australia and other countries since cases have dwindled in China, offering fewer human guinea pigs for testing.

"The hope is these neutralising antibodies can become a specialised drug that would stop the pandemic," he said.

China already has five potential coronavirus vaccines at the human trial stage, a health official said last week.

But the World Health Organization has warned that developing a vaccine could take 12 to 18 months.

Scientists have also pointed to the potential benefits of plasma -- a blood fluid -- from recovered individuals who have developed antibodies to the virus enabling the body's defences to attack it.

More than 700 patients have received plasma therapy in China, a process which authorities said showed "very good therapeutic effects".

"However, it (plasma) is limited in supply," Xie said, noting that the 14 neutralising antibodies used in their drug could be put into mass production quickly.

- Prevention and cure -

Using antibodies in drug treatments is not a new approach, and it has been successful in treating several other viruses such as HIV, Ebola and Middle East Respiratory Syndrome (MERS).

Xie said his researchers had "an early start" since the outbreak started in China before spreading to other countries.



Ebola drug Remdesivir was considered a hopeful early treatment for COVID-19 -- clinical trials in the US showed it shortened the recovery time in some patients by a third -- but the difference in mortality rate was not significant.

The new drug could even offer short-term protection against the virus.

The study showed that if the neutralising antibody was injected before the mice were infected with the virus, the mice stayed free of infection and no virus was detected.

This may offer temporary protection for medical workers for a few weeks, which Xie said they are hoping to "extend to a few months".

More than 100 vaccines for COVID-19 are in the works globally, but as the process of vaccine development is more demanding, Xie is hoping that the new drug could be a faster and more efficient way to stop the global march of the coronavirus.

"We would be able to stop the pandemic with an effective drug, even without a vaccine," he said.

Agence France-Presse

Friday, January 25, 2019

Blink-182, All Time Low frontmen form new band, drops first single ‘Drug’


MANILA, Philippines — Pop-punk band Blink-182’s Mark Hoppus and rock band All Time Low’s Alex Gaskarth have joined forces to form a new band called Simple Creatures and have released their first single “Drug.”

The pair announced the news on Thursday through a tweet on their new official Twitter account.


"Hi. We are Simple Creatures. We just woke up from a very long sleep. We have so much to tell you, but for the moment, all we can say is that we are glad you are here,” the tweet read.

Simple Creatures also dropped their first single titled “Drug” with a lyric video posted on Youtube.

Gaskarth expressed excitement to unveil this new band, saying: “This has been an insane journey. So unbelievably proud and excited to get this into the world. @markhoppus and I are here for you.”

Hoppus, on the other hand, said their debut EP is already on its way and will be released in March 2019.

“People!! So stoked to finally share this secret with the world. Alex and I started a band called @simplecreatures and our first single “Drug” is out Friday everywhere but you can listen to it here now! http://SimpleCreaturesMusic.com. EP1 out in March,” Hoppus said in a tweet.

Hoppus is the bassist, vocalist and last remaining original member of Blink-182, while Gaskarth is the lead vocalist and rhythm guitarist of All Time Low. /kga

source: entertainment.inquirer.net

Saturday, October 26, 2013

US approves more powerful, pure hydrocodone drug


WASHINGTON  — The U.S. Food and Drug Administration has approved a stronger, single-ingredient version of the painkiller hydrocodone, the widely-abused prescription medicine for chronic pain.

The agency said Friday it approved the pill Zohydro for patients with pain that requires “daily, around-the-clock, long-term treatment” that cannot be addressed with other drugs.

Hydrocodone is currently sold in combination pills like Vicodin to treat pain from injuries, surgery, arthritis, migraines and other ailments. The new drug from Zogenix is the first pure, non-combination form of the drug approved in the U.S.

The approval came as a surprise since the agency’s own panel of outside advisers gave the drug an overwhelmingly negative review last year. The agency’s panel of pain specialists voted 11-2, with one abstention, against approving the drug last December, questioning the need for a new form of one of most widely-abused prescription painkillers in U.S.

Zohydro’s approval was quickly criticized by patient safety advocates who had urged the FDA to reject the drug at a public meeting last year.

“We’re just going to kill more kids and then the FDA is going to come back and say, ‘oh, we made a mistake,’” said Avi Israel. Israel’s son Michael committed suicide in 2011 while struggling with painkiller addiction. Israel is the founder of a group called, Save the Michaels of the World, which aims to combat painkiller abuse in young people.

In 2011, U.S. doctors wrote more than 131 million prescriptions for hydrocodone, making it the most prescribed drug in the country, according to government figures. Hydrocodone pills also consistently rank among most-abused medicines in the U.S., according to the DEA.

The drug belongs to a family of medicines known as opiates or opioids because they are chemically similar to opium. They include morphine, heroin, oxycodone, codeine and methadone.

Friday’s news was also blasted by lawmakers in Congress who have been trying to rein in prescription drug abuse in their home states.

Rep. Bill Keating, a Democrat, said the FDA should have required the drug to contain anti-abuse design features that would make it harder for users to crush the pills and snort or inject them.

“FDA not only approves this dangerous drug, but does so without requiring any abuse-deterrent features. This is outrageous,” Keating said in a statement. “Abuse-deterrent technologies should not be the anomaly, they must be the norm.”

In recent years, Purdue Pharma, Pfizer Inc., Endo Health Solutions Inc. and other drugmakers have developed tamper-resistant versions of popular opioid drugs.

The timing of the FDA announcement also drew criticism from safety advocates and lawmakers. Only one day earlier the FDA said it would support stronger restrictions on combination drugs containing hydrocodone, including Vicodin and dozens of other generic formulations.

The drugs currently available mix hydrocodone with non-addictive pain relievers like aspirin and acetaminophen. For decades these drugs have been subject to less rigorous prescribing limits than other prescription painkillers like oxycodone.

Late Thursday, the FDA said it would recommend moving hydrocodone drugs from the schedule III class to the schedule II class of medications, a move that will limit the number of refills patients can receive and how many health professionals can prescribe the drugs.

The Drug Enforcement Administration had first asked the agency to take that step a decade ago, and lawmakers and safety advocates had increased their pressure on the agency in recent years.

Shares of Zogenix, Inc. jumped in trading Friday, climbing 80 cents, or 36 percent, to $3.04. Earlier shares set a 52-week high of $3.45.

source: business.inquirer.net