First conditional marketing authorization approval in the European Union for hemophilia "A" gene therapy
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New European Consortium - AGORA - launches to ensure access to life-saving gene therapies for children with rare diseases
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ERC Horizon Europe 2023 Submission Dates
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Review on ex vivo HSC gene therapy for Nature Rev Genetics
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Educational Resource: New Horizons in the Management of ADA-SCID
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Obituary Notice: Professor Shigetaka Asano
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Online Resource: New Horizons in the Management of ADA-SCID
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VIVEbiotech makes a capital increase of 3.5 million euros to complete its expansion plan
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This week in gene and cell therapy - 26 July 2019
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This week in gene and cell therapy - 19 July 2019
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This week in gene and cell therapy - 12 July 2019
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This week in gene and cell therapy - 5 July 2019
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This week in gene and cell therapy - 28 June 2019
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VIVEbiotech receives an issue notification of the patent grant for the LENTISOMA technology from the United States Patent and Trademark Office
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This week in gene and cell therapy - 21 June 2019
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This week in gene and cell therapy - 7 June 2019
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This week in gene and cell therapy - 31 May 2019
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This week in gene and cell therapy - 24 May 2019
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This week in gene and cell therapy - 17 May 2019
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This week in gene and cell therapy - 10 May 2019
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This week in gene and cell therapy - 3 May 2019
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This week in gene and cell therapy - 26 April 2019
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This week in gene and cell therapy - 12 April 2019
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This week in gene and cell therapy - 5 April 2019
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John Bell and Lisa Riedmayr win inaugural ESGCT PPE Award
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This week in gene and cell therapy - 8 March 2019
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This week in gene and cell therapy - 22 February 2019
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This week in gene and cell therapy - 15 February 2019
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This week in gene and cell therapy - 1 February 2019
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This week in gene and cell therapy - 25 January 2019
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This week in gene and cell therapy - 18 January 2019
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This week in gene and cell therapy - 4 January 2019
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This week in gene and cell therapy - 14 December 2018
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This week in gene and cell therapy - 7 December 2018
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Consensus statement of European Societies of Gene and Cell Therapy on the reported birth of genome-edited babies in China
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This week in gene and cell therapy - 23 November 2018
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This week in gene and cell therapy - 16 November 2018
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This week in gene and cell therapy - 9 November 2018
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This week in gene and cell therapy - 2 November 2018
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This week in gene and cell therapy - 7 September 2018
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This week in gene and cell therapy - 31 August 2018
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This week in gene and cell therapy - 24 August 2018
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This week in gene and cell therapy - 10 August 2018
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This week in gene and cell therapy - 20 July 2018
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This week in gene and cell therapy - 13 July 2018
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This week in gene and cell therapy - 6 July 2018
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This week in gene and cell therapy - 22 June 2018
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This week in gene and cell therapy - 15 June 2018
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This week in gene and cell therapy - 8 June 2018
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This week in gene and cell therapy - 1 June 2018
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This week in gene and cell therapy - 25 May 2018
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This week in gene and cell therapy - 18 May 2018
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This week in gene and cell therapy - 4 May 2018
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This week in gene and cell therapy - 27 April 2018
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This week in gene and cell therapy - 20 April 2018
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This week in gene and cell therapy - 6 April 2018
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Promising results of stem cell therapy for MS
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This week in gene and cell therapy - 9 March 2018
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This week in gene and cell therapy - 16 February 2018
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This week in gene and cell therapy - 2 February 2018
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This week in gene and cell therapy - 19 January 2018
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This week in gene and cell therapy - 12 January 2018
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This week in gene and cell therapy - 5 January 2018
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2017 breakthroughs in medicine dominated by gene and cell therapy
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FDA approved Luxturna, a gene therapy product for inherited blindness
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This week in gene and cell therapy - 8 December 2017
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This week in gene and cell therapy - 1 December 2017
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This week in gene and cell therapy - 24 November 2017
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This week in gene and cell therapy - 3 November 2017
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This week in gene and cell therapy - 27 October 2017
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New base editor extends machinery to correct single base pair mutations
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First FDA approval for CAR-T cell therapy
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First report of JCAR017 trial: CAR-T cell activity observed in the brain
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Gene addition of micro-dystrophin improves Duchenne muscular dystrophy symptoms in dogs
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Proof of concept for new strategy of genome editing to correct splice-site mutations
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Step forward for precision medicine - personalised anti-cancer vaccine tested in patients
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Genome editing used to treat Huntington's disease in mice
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Using genome editing to treat chronic inflammation
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New genome editing resources for patients and families
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First report from diabetes islet transplantation trial NCT02213003
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First clinical trial with in vivo genome editing
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Phase I trial of gene therapy for age-related macular degeneration completed
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ESGCT welcomes two Student Board Members
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Feng Zhang Discusses CRISPR and Future of Gene Editing in Interview in Human Gene Therapy
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