Prader-Willi Syndrome trials

Pioneering Progress for Rare Lives: Cell and Gene Therapy Trials in Pediatric Rare Disease Populations

Highlighting Fortrea’s commitment to advancing rare disease clinical research

Over the last 5 years, our team at Fortrea has supported more than 820 rare disease studies, each with its own challenges and complexities.

Advancing rare disease clinical trials and orphan drug research: A focus on APAC and China

Explore Fortrea's advancements in rare disease clinical trials and orphan drug research. Read our blog for insights into our innovative research solutions.

Empowering young voices in pediatric clinical trials: Fortrea’s commitment to child rights and participation

Learn about the experiences of the young participants involved in the clinical trials.

Rare diseases: A spotlight on Gaucher disease research in India

Explore Fortrea's focus on Gaucher disease research in India, addressing rare diseases with innovative treatment approaches.

Día de las Enfermedades Poco Comunes: celebramos los avances y la esperanza para el futuro

Join Fortrea in celebrating Rare Disease Day, highlighting progress in medical research and hope for the future.

Clinical trials in rare disease

Discover Fortrea's efforts in conducting clinical trials for rare diseases, aiming to develop effective treatments.