Sustainable funding models for rare disease treatments, and in particular gene therapies, must be explored to make sure that patients can gain access to these therapies, according to Claire Booth, professor in gene therapy and pediatric immunology at the UK’s UCL Great Ormond Street Institute of Child Health and Great Ormond Street Hospital (GOSH).
“We definitely need to explore these alternative models, because it’s just not commercially feasible [to develop drugs] for some of...







