EGT’s primary business is to address the unmet medical needs of patients with orphan diseases through the development of its technology and treatments. In addition, the company maintains a focused search for new therapeutic advancements that have the potential to be developed into future treatments. The company’s strong intellectual property position is the result of world-wide exclusive licensing agreements from prominent academic laboratories and the acquisition of proprietary technology.
Beta-thalassemia, also called Cooley’s Anemia, is a blood disease that effects thousands of Americans. In a major step toward a curative therapy, rare disease drug development firm Errant Gene Therapeutics, LLC (“EGT”) applauds the FDA approval of the Phase I Clinical Trial of a potentially curat...
Errant Gene Therapeutics, LLC (“EGT”), a pioneering boutique drug development firm specializing in Rare Diseases, applauds the FDA's approval of Phase I clinical trials for beta-thalassemia patients with autologous CD34+ cells transduced with TNS9.3.55. TNS9.3.55 is a cGMP vector technology previ...