Fast-Tracking Rare Disease: From Diagnosis to Custom Therapies

Join Professor Justin O’Sullivan (Liggins Institute, University of Auckland) as he shares his vision for a framework to support the progression from genomic diagnosis to truly individualized therapies for rare genetic conditions. The framework integrates phenotypic assessment, genomic and multi-omic evidence, and mechanistic understanding to inform key decisions, including therapeutic eligibility, modality selection, and clinical readiness. This framework aims to facilitate timely, safe clinical development of individualized therapies for rare disease.

Date: 4 May 2026

Time: 12:00 - 1:00pm

Place: Online. An invitation link will be sent to the email address provided