Prosensa is supported by a group of first-class venture capitalist as well as by a variety of other organizations. Funding from patient organizations as well as government subsidies have been an essential part in the growth of Prosensa as well and these organizations are seen as key partners of our company.

  • Other Investors

    • Aktion Benni & Co e.v.

      After Conny and Claus Over (Kreis Neuwied, Rheinland-Pfalz, Germany), parents of Benni, had been confronted with the diagnosis of their son´s disease, they decided to take action against this desperate situation. They founded "Aktion Benni & Co" in June 1996, in order to intensify investigation to cure Duchenne Muscular Dystrophy and to provide financial support. Many affected families from the whole of Germany have joined them from that moment.

      Aktion Benni & Co e.v. logo

    • Charley's Fund

      Charley’s Fund directs resources into the hands of researchers who have the best shot at developing a treatment or cure for Duchenne Muscular Dystrophy. Their goal is to cure DMD in time to save Charley’s life and the lives of thousands of boys like him.

      Charley's Fund logo

    • Villa Joep!

      Villa Joep is a Dutch foundation, started by the parents of Joep, which supports the research into therapeutic solutions for neuroblastoma in children, a very deadly and aggressive form of cancer.

      Villa Joep! logo

    • Senter Novem

      Senter Novem, an agency of the Ministry of Economical Affairs accomplishes professional execution of government policy in the range of innovation, environment, energy, sustainability, and provides links and synergy in between these items. Senter Novem supports and encourages companies, foundations and governments to reach social targets in these areas, both in national and international liaisons.

      Senter Novem logo

    • Duchenne Parent Project

      A Dutch foundation founded by parents of children that suffer from Duchenne Muscular Dystrophy in the Netherlands, aiming at research acceleration in order to heal or to find a treatment for Duchenne Muscular Dystrophy and to provide information to everybody involved with Duchenne Muscular Dystrophy patients.

      Duchenne Parent Project logo

    • Parent Project Muscular Dystrophy

      Parent Project Muscular Dystrophy’s mission is to improve the treatment, quality of life, and long-term outlook for all individuals affected by Duchenne Muscular Dystrophy (Duchenne) through research, advocacy, education, and compassion.

      Parent Project Muscular Dystrophy logo

    • CureDuchenne

      CureDuchenne is a non-profit organization founded in 2003 by Debra and Paul Miller, parents of a Duchenne boy. CureDuchenne’s vision is to cure Duchenne Muscular Dystrophy. CureDuchenne aggressively seeks the most promising, leading edge research breakthroughs and expedites them to the clinical trial process. The ultimate goal is give the boys that have Duchenne now a chance to live a normal life by expediting the cure and/or the availability of therapies that can give quality of life to Duchenne boys, much like insulin does for diabetics.

      CureDuchenne logo

    • AFM

      Created in 1958 by a group of patients and their families, and recognized as being of public utility in 1976, AFM (French Muscular Dystrophy Association) has a single objective: to defeat neuromuscular diseases which are devastating muscle-wasting diseases. It has set itself two missions: curing neuromuscular diseases and reducing the disabilities they cause.

      AFM logo