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82 results for "fda"
Scientists discovered an existing FDA-approved medication could prevent the deadliest part of breast cancer: when it spreads to other organs. The breakthrough offers new hope for patients with aggressive triple negative breast cancer.
A new artificial intelligence platform designed to improve post-surgical recovery just earned a major stamp of approval from federal regulators. RecovryAI's breakthrough designation from the FDA could accelerate how quickly patients get access to smarter recovery care.
The FDA just gave breakthrough status to its first generative AI chatbot for patients recovering from joint replacement surgery. This marks a major step forward in how artificial intelligence could help millions heal at home.
A new AI-powered virtual assistant that helps patients recover safely at home after surgery just earned FDA breakthrough status. The physician-prescribed tool could transform post-op care for millions of Americans now recovering outside hospitals.
The FDA just gave breakthrough status to the first generative AI chatbot designed to guide patients through recovery after joint replacement surgery. The move signals how AI could soon help millions of people heal better at home.
A groundbreaking gene-editing treatment could reach patients faster than ever before, as Prime Medicine asks the FDA to approve their therapy after just two successful treatments. The drug uses a revolutionary CRISPR technique to fix a genetic disorder that leaves patients vulnerable to deadly infections.
Children with a rare genetic disorder are developing normally thanks to an enzyme therapy crossing the blood-brain barrier. The FDA could approve the treatment this spring, offering hope to families worldwide.
After two decades of setbacks, scientists have achieved a major breakthrough with Lecanemab, the first fully approved treatment that actually slows Alzheimer's progression. Over 200 more potential treatments are now racing through clinical trials, bringing real hope to millions of families.
Scientists discovered that an FDA-approved cold plasma device triggers the body's natural healing process, speeding up surgical recovery while reducing fat tissue formation. Patients report firmer skin and faster healing after treatment.
The FDA just unveiled a breakthrough framework that could bring life-saving gene therapies to thousands of children with rare diseases in a fraction of the time. For families who've watched their kids suffer while treatments stall, this changes everything.
A heart condition once called a death sentence now has multiple FDA-approved treatments that are keeping patients alive and out of hospitals. Cardiac amyloidosis patients are being diagnosed earlier and living longer thanks to breakthrough medications approved in the past year.
Nigeria's food safety agency is proving that protective systems work when it matters most. While European formula brands face contamination concerns, Nigerian parents can breathe easy knowing local products remain safe.
Nemours Children's Hospital in Wilmington can now offer a groundbreaking one-time gene therapy that could give children with sickle cell disease a chance at a transformed life. The FDA-approved treatment addresses the root genetic cause of the disease that affects 100,000 Americans and shortens life expectancy by more than 20 years.
Families battling ultra-rare diseases just got a major breakthrough: the FDA announced a new pathway that will speed life-saving treatments to patients who've been told for decades "there aren't enough of you to study." A baby boy's miraculous CRISPR therapy inspired the change.
After decades of slow progress, ALS researchers at VCU Health say they're more optimistic about finding a cure than at any point in history. The Richmond team is combining new FDA-approved treatments with cutting-edge research to extend lives and find solutions.
The FDA just announced a new pathway that could bring life-saving gene editing treatments to patients with rare diseases in record time. For families battling conditions once considered untreatable, this could change everything.
A breakthrough artificial meniscus could help millions avoid painful knee replacement surgery. The FDA just gave it priority status to speed it toward patients.
The FDA just unveiled a new approval process that could bring life-saving treatments to millions of Americans with rare diseases in months instead of years. Families who've heard "wait for the science to catch up" finally have reason to hope.
The FDA just made it easier for life-saving gene therapies to reach patients with ultra-rare diseases who previously had few treatment options. The new pathway means families won't have to wait years for cures when the science shows real promise.
A newly approved medication could help people with Prader-Willi syndrome control the constant, overwhelming hunger that defines their daily lives. One mother shares why she's hopeful this treatment will give her son Robert a chance at greater independence and happiness.
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