Treatment seems to have been effective, but it is not clear whether such bespoke therapies can be widely applied.

An infant in Philadelphia has been successfully treated with a customized Crispr gene-editing therapy for a rare and deadly ...

An infant with a severe genetic condition has shown signs of improvement after receiving a gene-editing treatment tailored to ...

Health camp certifies 35 sickle cell patients for disability benefits, emphasizing prevention, early detection, and community support.

Experts make case for early testing, prevention and care In this report, VINCENT KURAUN explores the groundbreaking ...

Editas Medicine reports successful gene editing levels in stem cells, supporting potential treatment for sickle cell disease and beta thalassemia. Editas Medicine announced promising new data on ...

Despite making significant clinical progress, CRISPR Therapeutics (NASDAQ: CRSP) has been struggling financially in the past ...

The Michigan Sickle Cell Data Collection Program has been tracking information from the estimated 4,000 Michigan residents ...

Beam to Host Investor Webcast on Friday, June 13, 2025, at 4:00 p.m. ET ...

A baby born with a rare and dangerous genetic disease is growing and thriving after getting an experimental gene editing ...

The technique used on a 9½-month-old boy with a rare condition has the potential to help people with thousands of other ...