Advancing treatments for rare diseases together

February 2016

26Feb

EspeRare's innovative business model will be presented at the GPHI2 conference. On the 3rd and 4th March 2016, over 200 leaders from the business, humanitarian, health and academic sectors will gather at the IMD Business School in Lausanne to address priority issues in the field of health in Fragile Environments. Two key themes will take central stage of the event:

a) Ensuring and expanding access to health in fragile environments.
b) Enhancing the response to emerging and unmet needs.

For more follow this link 

23Mar

EspeRare Today achieves a significant milestone by enrolling patients with DMD in Rimeporide phase Ib trial:Our first DMD patient was recruited in France

Rimeporide, EspeRare's first programme reaches today a decisive clinical stage milestone. After encouraging preclinical results obtained in leading institutions and an orphan drug designation granted from the European Medicines Agency, the recruitment of patients with Duchenne Muscular Dystrophy from 6 to 14 years of age in a phase Ib study with Rimeporide started in Paris at the centre of I- Motion. Leading European neuro-paediatricians will be recruiting up to 20 patients with DMD in 2016 at the Armand Trousseau Hospital/ I-motion (Paris, France), the Great Ormond Street Hospital (London, UK), the Santa Creu i Sant Pau (Barcelona, Spain) and the San Raffaele Hospital (Milan, Italy).

This study is investigating the safety, tolerability, pharmacokinetics and pharmacodynamics of a 4-week treatment with rimeporide in these patients. In contrast to many therapeutics under development in DMD, rimeporide is indicated to all patients with DMD regardless of the causative mutations and age. To our knowledge, Rimeporide is one of the few clinical stage therapy intended to reduce inflammation and fibrosis both in skeletal muscles and in the heart.

 

Our hope is that Rimeporide may be a big step forward alone or in combination with other available treatments to address DMD including cardiomyopathy which at present is a progressive disease with very limited therapeutic options.

 

For more information see our website www.esperare.org/en/duchenne-programme and also www.clinicaltrials.gov