Scientists reprogram T Cells to target autoimmune diseasesThe non-viral technique is promising more specific therapies. By K. Filippidis, 07.11.2018
First human CRISPR study in the US could begin soonThe University of Pennsylvania has listed it in a medical trials directory.By D. Lumb, 01.18.2018
Gene therapy treatment for hereditary eye disease will cost $850,000The treatment’s developer is exploring a payment plan option.By M. Locklear, 01.03.2018
FDA OKs first gene therapy for hereditary diseaseLuxturna can treat a rare form of inherited blindness.By M. Moon, 12.20.2017
Gene therapy gives 'bubble babies' immune systemsThe new treatment restored all three major immune cell types in the babies.By S. Shah, 12.11.2017
New gene therapy technique saves boy's life by growing new skinEngineering and growing large amounts of skin this way could help others with the rare disease.By R. LeFebvre, 11.08.2017
Gene therapy for advanced lymphoma gets FDA approvalIt's the second approved gene therapy in the US.By M. Moon, 10.19.2017
First FDA-approved genetic therapy fights leukemiaThe procedure modifies a patient's autologous cells to target the cancer.By D. Lumb, 08.30.2017
First gene therapy drug proves a flop in the marketGlybera's $1 million price tag likely doomed it from the start.By J. Fingas, 04.23.2017
Stem cell-based cartilage could fix your broken hipThe living joint can even release anti-inflammatory molecules.By S. Dent, 07.21.2016
Blind woman may see thanks to gene therapy and lightOptogenetics are getting their first proper test in humans.By J. Fingas, 03.20.2016