TD Cowen 46th Annual Health Care Conference
Logotype for Ultragenyx Pharmaceutical Inc

Ultragenyx Pharmaceutical (RARE) TD Cowen 46th Annual Health Care Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Ultragenyx Pharmaceutical Inc

TD Cowen 46th Annual Health Care Conference summary

2 Mar, 2026

Angelman syndrome program updates

  • Aspire phase III study targets cognition as the primary endpoint, with a clinically meaningful difference set at five points and over 90% power for success based on modeling.

  • Homogeneous patient population with full deletions was chosen to minimize variability and placebo effect, excluding caregiver input in assessments.

  • Aurora study uses a basket approach to include broader genotypes and age ranges, aiming to support a broader label through extrapolation of safety and efficacy.

  • Both cognition and MDRI are considered primary endpoints, tested in parallel, with domain-specific meaningful score differences negotiated with the FDA.

  • Aurora is about 6–12 months behind Aspire in enrollment and progress.

Setrusumab and bone disease strategy

  • Statistically significant improvements in bone mineral density and vertebral fractures observed, with vertebral fractures validated as a key clinical endpoint.

  • Accelerated approval pathway is being considered, supported by clinical benefit and biomarker validation, with a confirmatory study planned.

  • Confirmatory study may focus on pain or fracture endpoints, likely to be larger and longer-term, with crossover extension considered helpful.

  • Accelerated approval is not expected to impact pricing or value, especially in rare diseases.

  • Label differentiation may rely on bone mineral density and vertebral fracture data.

Gene therapy and regulatory interactions

  • FDA feedback for Sanfilippo syndrome gene therapy focused on clinical data, with current delays due to manufacturing SOP documentation rather than new clinical data.

  • Resubmission after addressing SOPs will trigger a two-week validation and up to six-month review period.

  • Manufacturing for GSDIa is now in-house at Bedford, with validation period cleared and PDUFA date set.

  • SOP updates for GSDIa and other products can be done in parallel, with a phased approach to bringing manufacturing in-house.

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