Horama Joins Race To Develop Gene Therapies For Eye Diseases

Initial VC and institutional funding from a French syndicate will support further drug development at Paris-based Horama, which aims to put two targeted gene therapies for hereditary retinitis pigmentosa in the clinic by 2018.

Vision

The French company, Horama, which is working with specific serotypes of adeno-associated virus (AAV) that may have potential benefits as vectors for novel gene therapy approaches to retinopathies, has just appointed an experienced CEO Christine Placet and completed a smallish Series A to move two promising gene therapies into clinical studies, and to build up its drug development team.

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