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4532 results for "cell therapy"
A groundbreaking quality certification for cutting-edge immune cell therapies just passed its first inspection, opening the door for safer treatment expansion beyond cancer into autoimmune diseases. The framework ensures patients receive consistent, high-quality care as these life-changing therapies reach more people.
Children as young as 2 can now access a breakthrough gene therapy that could eliminate the need for lifelong blood transfusions. The FDA just expanded approval of Casgevy, a one-time CRISPR treatment that edits a patient's own cells to fight sickle cell disease.
Two researchers just won a $3 million Breakthrough Prize for discoveries that led to gene therapies functionally curing sickle cell disease and beta-thalassemia. Their work identified a genetic switch that helps patients' bodies produce healthy blood cells again.
A 41-year-old mother who spent her life battling sickle cell disease just became the first adult in Maryland to receive a potentially curative gene therapy using her own cells. After decades of hospital stays and missing family moments, Jessica Ceja now has hope for a life without the painful disease.
Two scientists just won a $3 million prize for discovering how to switch on healthy blood cells in people with sickle cell disease. Their breakthrough has led to gene therapies that functionally cure patients who once faced lifelong pain.
A breakthrough gene editing treatment has achieved what doctors call a "functional cure" for sickle cell disease, with 27 out of 28 patients experiencing zero painful crises after receiving the therapy. The one-time treatment edits patients' own blood cells to correct the genetic mutation, offering new hope for 100,000 Americans living with this painful disease.
Chinese scientists used stem cell therapy to completely reverse type 2 diabetes in a patient for the first time ever. The breakthrough treatment eliminated the patient's need for insulin injections by regrowing healthy pancreatic cells.
AstraZeneca is partnering with robotics company Multiply Labs to automate the complex process of making cell therapies, potentially making these breakthrough treatments accessible to more patients. The collaboration could transform how these powerful medicines reach people who need them.
Scientists have successfully reversed heart failure damage using engineered immune cells, offering hope to millions. The therapy reduced scarring and restored heart function in both animal and primate studies without harmful side effects.
A breakthrough cell therapy cut the death rate in half for patients with advanced liver disease, offering hope beyond transplants. After four years, 70% of patients treated were alive without needing a transplant, compared to just 40% who received standard care.
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.
Scotland just approved a groundbreaking gene therapy that lets sickle cell patients get treatment without needing a matching donor. Four other life-changing treatments for cancer and blood disorders also got the green light.
After decades of research, gene therapy is bringing lasting relief to sickle cell patients after just one treatment. UCLA researchers are leading the charge to cure a disease that affects 100,000 Americans.
A Louisiana man just became the first person in the state to be functionally cured of sickle cell disease using advanced gene therapy. The breakthrough offers hope to thousands living with the painful genetic blood disorder.
A 24-year-old who lost his sister to sickle cell disease just became the first Michigan patient cured by groundbreaking gene therapy. Chantez Sanford is heading back to college healthier than he's ever been.
A boy with autism who grew up unsure if he'd eat the next day now runs a global stem cell therapy network helping patients once told "there's nothing more we can do." Prof Dr Mike Chan's Malaysian facility is reversing conditions from Parkinson's to kidney failure. ---
Scientists at Harvard Medical School built an AI system that could finally make lab-grown cell therapies predictable enough for widespread use. The breakthrough tackles the biggest obstacle keeping regenerative medicine from reaching patients who need it.
A Louisiana man with lifelong sickle cell disease received groundbreaking gene therapy that eliminated his symptoms and opened the door to his dream career as a pilot. His story represents hope for thousands living with this painful genetic condition.
Twenty-seven out of 28 patients with severe sickle cell disease are now living pain-free after a groundbreaking gene editing treatment. The one-time therapy is offering new hope to people living with a genetic disorder that typically shortens life expectancy to the mid-40s.
A Maryland mother who spent years in and out of hospitals every month is now living pain-free after becoming the first woman in her state to receive groundbreaking gene therapy for sickle cell disease. Clinical trials show up to 93% of patients stopped experiencing severe pain crises.
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