Last updated on February 2018

Long-term Evaluation on Height and Weight in Patients With MPS II Who Started Treatment at < 6 Years of Age

Brief description of study

This long-term study will provide Elaprase treatment to children enrolled in this study and will utilize data from both enrolled patients and Hunter Outcome Survey (HOS) patient registry data to conduct the primary growth analysis to assess changes in height and weight in patients with Mucopolysaccharidosis II (Hunter syndrome) MPS II.

Clinical Study Identifier: NCT02455622

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Barbara Burton

Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, IL United States
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Ceila Pérez de Ferrán

Hospital Infantil Dr Robert Reid Cabral
Santo Domingo, Dominican Republic
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Julia Hennermann

Universit tsmedizin der Johannes Gutenberg-Universit t Mainz
Mainz, Germany
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Lock Hock Ngu

Hospital Kuala Lumpur
Kuala Lumpur, Malaysia
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Fathiya Al Murshedi

Sultan Qaboos University Hospital
Sultanate of Oman, Oman
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Mary Anne Chiong

Philippine General Hospital
Manila, Philippines
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Moeen AlSayed

King Faisal Specialist Hospital & Research Centre
Riyadh, Saudi Arabia
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Maja Djordjevic

Mother and Child Health Care Institute of Serbia Dr Vukan Cupic
Beograd, Serbia
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Kanya Suphapeetiporn

Chulalongkorn University
Bangkok, Thailand
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Vu Chi Dung

National Pediatrics Hospital
Hanoi, Vietnam
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