Paris, May 15, 2018 – Horama, a French biotech company based in Paris and Nantes, is a spin-off of Philippe Moullier’s laboratory and a member of Atlanpole Biotherapies Western France biocluster. Horama, which specialises in gene therapy for the treatment of rare, inherited retinal diseases, announces today the appointment of Dr Russell Greig, as Chairman of the Board of Directors. Dr Russell Greig will succeed Thierry Laugel who served as Chairman since the last Series B financing round in November 2017.
Dr Russell Greig worked at GlaxoSmithKline for three decades, most recently as President of SR One, GlaxoSmithKline’s corporate venture group. Prior to joining SR One, he served as President of GlaxoSmithKline’s Pharmaceuticals International from 2003 to 2008 as well as serving on the GlaxoSmithKline corporate executive team.
Currently, Dr Russell Greig serves as Chairman of Ablynx (Belgium), and of both AM Pharma and Mint Solutions in the Netherlands, eTheRNA in Belgium, and Sanifit in Spain.
He was previously Chairman of Isconova in Sweden (acquired by Novavax, United States), Novagali in France (acquired by Santen, Japan), Syntaxin in the United Kingdom (acquired by Ipsen, France) and Onxeo Pharma (previously BioAlliance Pharma) in France, and a venture partner at Kurma Partners (Paris, France). Finally, Dr Russell Greig was also a member of the Scottish Scientific Advisory Committee, reporting to the First Minister of Scotland.
Commenting on his appointment, Dr Russell Greig stated, “I am pleased to join Horama and contribute to making treatments available in the future for rare ophthalmological diseases. Horama is a very promising French company which, with its innovative approach in gene therapy, develops treatments for diseases such as retinitis pigmentosa for which there is currently no treatment.”
Christine Placet, CEO of Horama and Thierry Laugel, former Chairman of the Board added: “We are pleased that Russell Greig is joining us. His huge experience in the pharmaceutical industry will be invaluable in maximising the potential of our gene-therapy platform.”