03 Profile
Hansard to 12 November 2026 · 31,484 contributions indexed · 1,439 MPs & peers
All voices01 Voice · Academic · Rare diseases
Emil Kakkis, M.D., Ph.D.
CEO of Ultragenyx
Quoted in the press, across 1 topic since 3 Sept 2026
02 Quoted on · 1 of 29 topics
Emil Kakkis, M.D., Ph.D.: key facts
- Kind of voice
- Academic
- Role
- CEO of Ultragenyx
- Quoted on
- Rare diseases
- Press coverage
- Quoted in the press
- Most recently quoted
- 17 Sept 2026
- First quoted
- 3 Sept 2026
04 The signal · where Emil Kakkis, M.D., Ph.D. sits on rare diseases
Quoted
Quoted in the press on rare diseases.
Placed by press coverage on this topic only, not across all topics.
- Giles LomaxSector leaderChief Executive Officer, Spinal Muscular Atrophy UK (SMA UK)Leading
- Dr Harrison CarterAcademicDirector of Screening at NHS EnglandLeading
- Dr Rich ScottSector leaderChief Executive Officer of Genomics EnglandLeading
- Laurent ServaisClinicianProfessor, University of Oxford; children's doctor and expert in rare muscle-wasting diseases
David LiuAcademicThomas Dudley Cabot Professor of the Natural Sciences at Harvard, the Broad Institute, and the Howard Hughes Medical Institute- Emil Kakkis, M.D., Ph.D.AcademicCEO of Ultragenyx
- Jim Flett WilsonAcademicProfessor of human genetics, University of Edinburgh Usher Institute
- Iain HorrocksClinicianConsultant Paediatric Neurologist at NHS Greater Glasgow and Clyde
Showing the leading voices and those placed around Emil Kakkis, M.D., Ph.D. · See every voice on the topic →
05 On the record · press
What Emil Kakkis, M.D., Ph.D. has said
- blockonomi.com
- fiercepharma.com
Where Emil Kakkis, M.D., Ph.D. has been quoted
- FDA approves Ultragenyx’s gene therapy Fayuvi for rare neurodegenerative disorderfiercepharma.com · 17 Sept 2026
- Ultragenyx (RARE) Shares Plunge 45% Following Critical Drug Trial Failureblockonomi.com · 3 Sept 2026
How we found the articles that name Emil Kakkis, M.D., Ph.D.: we searched news for these terms.
- rare disease
- rare conditions
- orphan drugs
- genetic disorder
- cystic fibrosis
- motor neurone disease
- muscular dystrophy
- Huntington
Also searched with “rare disease” in each of 8 national papers. Every term for Rare diseases
Verbatim
“We recognize the profound urgency of making this therapy available to families, and our focus now is on supporting timely access in the U.S. as we work closely with treatment centers and payers to support families on the gene therapy treatment journey.”
“We are disappointed for the global patient community who has invested so much in early-stage research.”
Related media coverage
Recent UK press coverage of their topics, not necessarily citing them directly.
Professors, researchers and think-tank analysts quoted on the strength of their research rather than a clinical role. Citations are counted by an automated scan of UK press coverage and may be incomplete. Roles, biographies and contact details are researched and human-reviewed before they appear here; anything not yet reviewed is simply absent rather than shown unverified. This profile was last updated on 12 Nov 2026. See the methodology for how this page is built, or email contact@bridgeheadcommunications.com to correct anything on it.