Errant Gene Therapeutics, LLC
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.
POSTED
11-13-12
Beta-Thalassemia Treatment Approved For FDA's Clinical Phase I Trials
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...
POSTED
08-14-12
EGT Welcomes FDA Clinical Phase I Trial Approval
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...
