AbstractBackground and methodsWorkpackage 4 of EuroCareCF brought together a group of small and middle-size companies (SMEs) with strong interest in drug development for cystic fibrosis (CF). The common interest of SMEs and patient organizations (PO) in mutually beneficial cooperation was assessed. This was achieved by identifying critical unmet medical needs of CF patients and by analyzing fields of cooperation between SMEs and POs.ResultsOver and above all, finding a cure for the disease is considered the most important unmet medical need by POs. However, preventing or slowing down any further deterioration of health and the alleviation of symptoms are also considered valuable objectives. Areas of co-operation with SMEs include the prepar...
The first regulatory approval for a drug developed specifically for cystic fibrosis (CF) occurred in...
Introduction: For the optimal management of children with cystic fibrosis, there are currently no ef...
This is the second in a series of four papers updating the European Cystic Fibrosis Society (ECFS) s...
AbstractBackground and methodsWorkpackage 4 of EuroCareCF brought together a group of small and midd...
AbstractBackgroundSeveral guidelines for cystic fibrosis (CF) caregivers exist, but information abou...
AbstractThe care and condition of people with cystic fibrosis (CF) in 34 European countries is repor...
AbstractA significant increase in life expectancy in successive birth cohorts of people with cystic ...
Cystic fibrosis, the most common of rare diseases, has been mobilizing healthcare professionals and ...
AbstractWe describe the rationale for disease specific research networks in general as well as the a...
A significant increase in life expectancy in successive birth cohorts of people with cystic fibrosis...
Aims Cystic Fibrosis (CF) is a rare, chronic, progressive, multi-organ disease. It needs life-long,...
AbstractIn patients with cystic fibrosis (CF), clinical trials are of paramount importance. Here, th...
We describe the rationale for disease specific research networks in general as well as the aims and ...
AbstractSince the earliest days of cystic fibrosis (CF) treatment, patient data have been recorded a...
International audienceThe objective of this study consist in displaying sociotechnical implementatio...
The first regulatory approval for a drug developed specifically for cystic fibrosis (CF) occurred in...
Introduction: For the optimal management of children with cystic fibrosis, there are currently no ef...
This is the second in a series of four papers updating the European Cystic Fibrosis Society (ECFS) s...
AbstractBackground and methodsWorkpackage 4 of EuroCareCF brought together a group of small and midd...
AbstractBackgroundSeveral guidelines for cystic fibrosis (CF) caregivers exist, but information abou...
AbstractThe care and condition of people with cystic fibrosis (CF) in 34 European countries is repor...
AbstractA significant increase in life expectancy in successive birth cohorts of people with cystic ...
Cystic fibrosis, the most common of rare diseases, has been mobilizing healthcare professionals and ...
AbstractWe describe the rationale for disease specific research networks in general as well as the a...
A significant increase in life expectancy in successive birth cohorts of people with cystic fibrosis...
Aims Cystic Fibrosis (CF) is a rare, chronic, progressive, multi-organ disease. It needs life-long,...
AbstractIn patients with cystic fibrosis (CF), clinical trials are of paramount importance. Here, th...
We describe the rationale for disease specific research networks in general as well as the aims and ...
AbstractSince the earliest days of cystic fibrosis (CF) treatment, patient data have been recorded a...
International audienceThe objective of this study consist in displaying sociotechnical implementatio...
The first regulatory approval for a drug developed specifically for cystic fibrosis (CF) occurred in...
Introduction: For the optimal management of children with cystic fibrosis, there are currently no ef...
This is the second in a series of four papers updating the European Cystic Fibrosis Society (ECFS) s...