Health
New AI-generated COVID drug enters Phase I clinical trials: ‘Effective against all variants’
Artificial intelligence is increasingly moving into the health care arena and helping to streamline medical processes — including the creation of new drugs.
Insilico Medicine, an AI-driven biotech company based in Hong Kong and in New York City, recently announced that its new AI-designed drug for COVID-19 has entered Phase I clinical trials.
This oral drug is a treatment, not a vaccine. If approved, it would become the first-ever alternative to Paxlovid, noted Alex Zhavoronkov, PhD, founder and CEO of Insilico Medicine.
WHAT IS ARTIFICIAL INTELLIGENCE?
“Generative AI is transforming every area of human development,” said Zhavoronkov in a press release announcing the new discovery.
“We’re extremely happy to announce that our second small molecule therapeutic — generated using generative AI — is now entering human clinical trials.”
Paxlovid, which is currently the only medication available to treat COVID symptoms, has been linked to some undesirable side effects, Insilico noted.
One of these is “Paxlovid rebound,” which is when patients recover from COVID and test negative — but then test positive again a short time later.
Another documented side effect, “Paxlovid mouth,” occurs when the drug leaves an unpleasant taste in the mouth for those who take it.
“Generative AI is transforming every area of human development.”
An additional limitation of Paxlovid is that as COVID mutates, drug-resistant strains can emerge.
FIRST AI-GENERATED DRUG ENTERS HUMAN CLINICAL TRIALS, TARGETING CHRONIC LUNG DISEASE PATIENTS
Insilico’s new pill has been shown to be effective against variants that are resistant to Paxlovid, and is also more stable and works for a longer period of time, according to Zhavoronkov.
In preclinical studies, ISM3312 “significantly reduced” viral load in lung tissue and decreased lung inflammation, the company stated in the release.
To create its new drug, Insilico’s research team first used its target discovery platform, PandaOmics, to identify the target protein within the coronavirus.
Next, it used its in-house “generative chemistry platform,” Chemistry42, to generate new molecules that would attack that protein as a means of treating COVID and other coronaviruses.
One “hit molecule,” called ISM3312, was shown to be effective in February 2020.
The company then filed a patent application for the drug in April 2020.
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“The drug has been shown to be effective against all variants, as well as other types of coronaviruses that cause diseases, including severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS),” Zhavoronkov told Fox News Digital.
Insilico’s newly discovered molecule has been shown to have “broad antivirus activity against multiple strains and variants,” he said.
Another benefit is that the new drug will be easy to produce in large quantities, according to Zhavoronkov.
“Our molecule requires only a two-step process using simple, commercially available starting materials,” he said.
ISM3312 is currently being evaluated in a Phase 1 study to assess the safety and tolerability of the drug in healthy volunteers.
AI-DISCOVERED DRUG SHOWS ‘ENORMOUS POTENTIAL’ TO TREAT SCHIZOPHRENIA: ‘REAL NEED FOR BETTER TREATMENT’
The compound is also currently being tested against the EG.5 COVID variant.
The results of the clinical trials are expected to be released by the end of 2023.
“Following the completion of the Phase 1 healthy volunteer study, further decisions will be made about testing the compound in coronavirus-infected patients,” said Zhavoronkov.
Insilico’s research team believes its new drug is a prime example of how AI is helping to accelerate new, more effective treatments for COVID.
“We cannot afford to dismiss COVID as a problem of the past,” Zhavoronkov told Fox News Digital.
He added, “Generative AI offers us a powerful tool for accelerating the drug discovery process and allows us to quickly identify new solutions that we hope can provide more potent defenses against mutating COVID strains and prevent another pandemic.”
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Dr. Harvey Castro, a Dallas, Texas-based board-certified emergency medicine physician and national speaker on artificial intelligence in health care, was not involved in the research but agreed that ISM3312 represents a “significant step forward” in the fight against COVID-19 and the use of AI for drug discovery.
He pointed out, however, that “doctors should remain cautious.”
“For health care providers, the advent of AI-generated drugs like ISM3312 opens up new avenues for treatment — but it’s crucial to stay updated on the clinical trials and research data for ISM3312 and consider the patient’s existing medication regimen before prescribing a new drug,” he told Fox News Digital.
For patients, Castro said ISM3312 “represents hope.”
He said, though, that “it’s essential to consult health care providers for personalized advice and stay informed about the latest research and clinical trial results for the drug.”
Said Castro as well, “While this new drug offers a promising alternative to treating the virus, more extensive clinical trials and global regulatory approvals are needed to confirm its efficacy and safety.”
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Health
FDA bans red food dye due to potential cancer risk
The U.S. Food and Drug Administration (FDA) has officially banned red dye — called Red 3, or Erythrosine — from foods, dietary supplements and ingested medicines, as reported by the Associated Press on Wednesday.
Food manufacturers must remove the dye from their products by January 2027, while drug manufacturers will have until January 2028 to do so, AP stated.
Any foods imported into the U.S. from other countries will also be subject to the new regulation.
RED FOOD DYE COULD SOON BE BANNED AS FDA REVIEWS PETITION
“The FDA is taking action that will remove the authorization for the use of FD&C Red No. 3 in food and ingested drugs,” said Jim Jones, the FDA’s deputy commissioner for human foods, in a statement.
“Evidence shows cancer in laboratory male rats exposed to high levels of FD&C Red No.3,” he continued. “Importantly, the way that FD&C Red No. 3 causes cancer in male rats does not occur in humans.”
The synthetic dye, which is made from petroleum, is used as a color additive in food and ingested drugs to give them a “bright cherry-red color,” according to an online statement from the FDA.
The petition to ban the dye cited the Delaney Clause, which states that the agency cannot classify a color additive as safe if it has been found to induce cancer in humans or animals.
The dye was removed from cosmetics nearly 35 years ago due to potential cancer risk.
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“This is a welcome, but long overdue, action from the FDA: removing the unsustainable double standard in which Red 3 was banned from lipstick but permitted in candy,” said Dr. Peter Lurie, director of the group Center for Science in the Public Interest, which led the petition effort, as reported by AP.
Dr. Marc Siegel, clinical professor of medicine at NYU Langone Health and Fox News senior medical analyst, applauded the FDA’s ban.
“It was a long time coming,” he told Fox News Digital. “It’s been more than 30 years since it was banned from cosmetics in the U.S. due to evidence that it is carcinogenic in high doses in lab rats. There needs to be a consistency between what we put on our skin and what we put into our mouths.”
“There needs to be a consistency between what we put on our skin and what we put into our mouths.”
Siegel said he believes the FDA’s decision could be tied to the incoming new head of the Department of Health and Human Services, Robert F. Kennedy Jr.
“They knew it would have happened anyway under RFK Jr.,” he said. “It is already banned or severely restricted in Australia, Japan and the European Union.”
The food additive also “drew kids in” to a diet of empty calories and ultraprocessed foods, Siegel added.
“It has also been linked to behavioral issues in children, including ADHD.”
Nearly 3,000 foods are shown to contain Red No. 3, according to Food Scores, a database of foods compiled by the Environmental Working Group.
For more Health articles, visit www.foxnews.com/health
The National Confectioners Association provided the below statement to Fox News Digital.
“Food safety is the number one priority for U.S. confectionery companies, and we will continue to follow and comply with FDA’s guidance and safety standards.”
The petition to remove Red No. 3 from foods, supplements and medications was presented in 2022 by the Center for Science in the Public Interest and 23 other organizations and scientists.
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