A Phase 2 Study to Evaluate the Dose and Pharmacodynamic Efficacy of Sialic Acid-Extended Release (SA-ER) Tablets in Patients With GNE Myopathy or Hereditary Inclusion Body Myopathy (GNE Myopathy)
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ClinicalTrials.gov Identifier: NCT01517880 |
Recruitment Status
:
Completed
First Posted
: January 25, 2012
Last Update Posted
: June 16, 2016
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Sponsor:
Ultragenyx Pharmaceutical Inc
Information provided by (Responsible Party):
Ultragenyx Pharmaceutical Inc
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No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : | Completed |
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Actual Primary Completion Date : | November 2013 |
Actual Study Completion Date : | November 2013 |
Certification/Extension First Submitted : | June 14, 2016 |