
Through the CTRM acquisition, Aastrom is acquiring global commercial rights to three marketed autologous cell therapy products. Carticel (autologous cultured chondrocytes) is an autologous chondrocyte implant (ACI) currently marketed in the United States for the treatment of articular cartilage defects. Epicel (cultured epidermal autografts) is a permanent skin replacement for full thickness burns greater than or equal to 30% of total body surface area, and is marketed in countries around the world. MACI (matrix-induced autologous chondrocyte implant) is a third-generation ACI product currently marketed in the European Union. Revenues of those three products were $44 million in 2013. Aastrom will also acquire global manufacturing and production centers located in the United States and Denmark.
“The acquisition of Sanofi’s CTRM business is a transformative transaction that positions Aastrom as a fully-integrated global regenerative medicine company,” said Nick Colangelo, president and chief executive officer of Aastrom. “The CTRM business brings us global manufacturing, marketing and sales capabilities that are structured to support the current portfolio of marketed products as well as our future product development plans. This transaction also provides us with a platform to generate operating income to support the development of our high-potential pipeline products and continued growth through additional strategic transactions.”
“Sanofi’s CTRM business, a pioneering organization with more than 20 years of experience in cell therapy and regenerative medicine, developed and marketed some of the first regenerative medicine products in the world,” continued Colangelo. “We look forward to working with the talented CTRM team to build Aastrom into the leading cell therapy company in the regenerative medicine field.”
Sanofi acquired the CTRM business in 2011 through the acquisition of Genzyme Corp.
Carticel was approved by the FDA in 1997 and has had more than 22,000 implants performed since that time. MACI is a third-generation ACI product commercially available in the European Union since 1998, with more than 10,000 patients treated to date. Epicel is approved for use as a humanitarian use device in the United States and supplied to patients outside the United States on a named-patient basis.
Date: April 21, 2014
Source: Aastrom