by Hellen Houlleberghs | May 22, 2025 | Blog
Clinical trials play a vital role in developing new treatments and medications. However, when children are involved, the process becomes significantly more complex. Children are considered a vulnerable population, requiring careful ethical, regulatory, and...
by Hellen Houlleberghs | Apr 14, 2025 | Blog
At Orfenix, our mission is to develop therapies for unmet medical needs. One such need is a treatment for pseudoxanthoma elasticum (PXE), a rare genetic disorder that significantly impacts patients’ lives. Heleen van Loenen, head of the Dutch PXE patient organisation,...
by Ivo De Nooijer | Mar 20, 2025 | Blog
We at Orfenix are committed to socially responsible pharmaceutical practices. These practices emphasize balancing innovation with accessibility, long-term pharmaceutical sustainability, and equity. These principles drive efforts to create strategic public-private...
by Vincent Van der Wel | Feb 11, 2025 | Blog
Over the past decades its popularity has increased, especially amongst academics. In 2010, there were only 57 publications on drug repurposing. By 2024, this number has increased to over 2300 publications, reflecting the increased interest and activity in the field of...
by Hellen Houlleberghs | Jan 9, 2025 | Blog
The main challenges encountered during clinical trials include patient recruitment and retention, but also regulatory hurdles and methodological complexities need to be overcome. Drug repurposing is one of the possibilities used by Orfenix that aims to ease the...
by Hellen Houlleberghs | Nov 21, 2024 | Blog
Understanding EMA scientific advice The European Medicines Agency (EMA) scientific advice procedure was introduced with the aim to improve communication between companies developing medicinal products (sponsors) and regulators to enable streamlining of the development...
