Theratechnologies appoints new ceo
John-Michel Huss has more than 20 years’ experience in the pharmaceutical industry
Until recently, Huss was chief of staff, in the office of the ceo, at Sanofi-Aventis in Paris. He has more than 20 years’ experience in the pharmaceutical industry in various international positions and was responsible for various disease areas including diabetes and metabolism.
Huss began his career in 1990, at Merck & Co, primarily in sales and marketing in the US, Germany and Switzerland. In 1996, he was offered a position with F. Hoffman-La Roche as an internal product manager at its Basel headquarters in Switzerland. From there in 1999, he joined Sanofi-Synthélabo as business unit director and has held various positions of increasing responsibility in marketing and sales. He became general manager in Switzerland in 2007.
During his tenure at Sanofi-Aventis (Sanofi-Synthélabo merged with Aventis in 2004) Huss held positions in Germany, Canada, Switzerland and France.
‘I am honoured to have been chosen as Theratechnologies' president and ceo,’ said Huss.
‘The company has done an outstanding job of developing an exciting new compound, tesamorelin, and navigating it through the final regulatory stages of the drug development process.’
You may also like
Manufacturing
BD and Suttons Creek collaborate to streamline combination product development for pharma and biotech
The new strategic collaboration will help pharmaceutical and biotech companies reduce development risk and regulatory complexity across drug-device combination products, including biologics and GLP-1 therapies
You need to be a subscriber to read this article.
Click here to find out more.
Click here to find out more.
Regulatory
UK clinical trial reforms come into force in largest regulatory overhaul in 20 years
The MHRA and Health Research Authority are implementing the most significant package of clinical trial regulatory reforms in more than two decades, introducing faster assessment routes for lower-risk trials and mandatory registration of trial results
Regulatory
FDA grants Orphan Drug Designation to pegrizeprument for prevention of heart transplant rejection
The FDA has granted Orphan Drug Designation to pegrizeprument (VEL-101), a novel monoclonal antibody fragment licensed to Veloxis Pharmaceuticals, for the prevention of heart allograft rejection, following a similar designation granted for liver transplant rejection in January 2026
Research & Development
Epitopea receives MHRA approval for first-in-human trial of RNA vaccine for ovarian cancer
The company has received regulatory approval from the MHRA and Regional Ethics Committee to initiate its OVACT Phase I/Ib clinical trial of CryptiVax-1001, an off-the-shelf mRNA immunotherapy targeting high-grade serous ovarian cancer
Manufacturing
Cipla receives FDA approval for first AB-rated generic of Ventolin HFA in $1.5bn US albuterol market
Indian pharmaceutical company Cipla has secured final FDA approval for its Albuterol Sulfate Inhalation Aerosol, becoming the first AB-rated generic therapeutic equivalent of GlaxoSmithKline's Ventolin HFA