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A Multicenter, Multinational Clinical Assessment Study for Pediatric Patients With Achondroplasia

Eligibility


Ages Eligible for Study: 0 Years to 16 Years
Genders Eligible for Study: All
Accepts Healthy Volunteers: No
Sampling Method: Probability Sample

Study Population



  • Approximately 250 patients will be enrolled.

  • Patients aged 0 to 16 years, inclusive, on the date of consent will be enrolled. Patients aged 0 to < 4.5 years on the date of consent may also be enrolled, the timing of which will be at the discretion of the sponsor. Approximately equal numbers of boys and girls will be enrolled.
Please read here what the inclusion and exclusion criteria are.

Contacts


Contact:  Trial Specialist     E-mail:  This email address is being protected from spambots. You need JavaScript enabled to view it.  

Please refer to this study by its ClinicalTrials.gov identifier: NCT01603095

Locations


United States, California


Harbor-UCLA Medical Center

 


Los Angeles, California, United States, 90048


Contact: Nathalia Patritti Cressey, Study Coord      310-781-3682 ext Office


Contact      310-597-1960 ext Cell      -  Principal Investigator: Patti Dickson, MD


Children's Hospital and Research Center Oakland

   

Oakland, California, United States, 94609


Contact: Jacqueline Madden, Study Coord      510-428-3885 ext 5745

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United States, Delaware


Nemours/Alfred I. duPont Hospital for Children

 

Wilmington, Delaware, United States, 19803


Contact: Cassie Brown, Study Coord      302-298-7930

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Contact: Michael Bober, MD


United States, Georgia


Emory University

 

Decatur, Georgia, United States, 30033


Contact: Elizabeth Smith, Study Coord

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Contact: William Wilcox, MD

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United States, Illinois


Ann and Robert H Lurie Children's Hospital of Chicago

 

Chicago, Illinois, United States, 60614


Contact: Victoria Sanders, Study Coord    312-227-6120


United States, Maryland


Johns Hopkins McKusick- Institute of Genetic Medicine

 

Baltimore, Maryland, United States, 21287


Contact: Adekemi Alade, Study Coord

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Contact: Kira Lurman, Study Coord

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United States, Missouri


University of Missouri

 

Columbia, Missouri, United States, 65201


Contact: Vicki L Jones, Study Coord      573-882-7583

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Contact: Daniel G Hoernschemeyer, MD      573-882-1351


Principal Investigator: Daniel G Hoernschemeyer, MD


United States, Tennessee


Vanderbilt University

 

Nashville, Tennessee, United States, 37232


Contact: LeeAnna Melton, Study Coord      615-343-6761

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United States, Texas


Baylor College of Medicine

 

Houston, Texas, United States, 77030


Contact: Catherine Loffredo, Study Coord

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Australia, Victoria


Murdoch Children's Research Institute

 

Enrolling by invitation

Parkville, Victoria, Australia, 3052


France


Institut Necker

 

Paris, France, 75015


Contact: Kim-Hahn Le Quan Sang, MD      33 1 44 49 59 51

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Principal Investigator: Valerie Cormier-Daire, MD


United Kingdom


Guy's and St. Thomas NHS Foundation Trust Evelina Children's Hospital

 

London, England, United Kingdom, SE1 9RT


Contact: Joanna Poulter, Study Coord      020 7188 7188 ext 52237

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Principal Investigator: Melita Irving, MD

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