When she was born, doctors informed Opal Sandy’s parents that their child would never hear. At the age of 11 months, she had ...

Elania is one of 59 children born with ADA-SCID who have been cured using this gene therapy, which will soon be submitted for ...

A new study has brought scientists one step further in the direction of developing a cure for a brutal group of rare brain ...

Long-term follow-up shows 95% success rate, no serious complications in largest ADA-SCID gene therapy study to date ...

The goal of gene therapy is to permanently cure hereditary diseases. One of the most promising technologies for this is the ...

AGC Biologics, your friendly CDMO expert, announced an agreement to provide comprehensive development and manufacturing for Rarity PBC's gene therapy.

A one-time gene therapy using a patient’s own stem cells has effectively cured a deadly immune disorder in 95% of treated ...

Oncologists' experience with CGT has increased, with more patients treated and earlier lines of therapy being utilized.

Endocrine therapy typically slows cell cycle progression by reducing cyclin D1, which partners with CDK4/6 to promote cell ...

Researchers at Texas A&M’s Health Science Center have developed a photo-inducible binary interaction tool, or PhoBIT, system ...

Dr. Singh underscored India’s remarkable progress in the biotechnology and pharmaceutical sectors, calling it a key driver of ...