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RG2133 (2',3',5'-Tri-O-Acetyluridine) in Mitochondrial Disease

This study has been terminated.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00060515
First Posted: May 8, 2003
Last Update Posted: December 9, 2005
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Repligen Corporation
  Purpose
The objective of the study is to determine the safety and tolerability of RG2133 in patients with Mitochondrial Disease.

Condition Intervention Phase
Mitochondrial Diseases Drug: RG2133 (2',3',5'-tri-O-acetyluridine) Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Primary Purpose: Treatment
Official Title: An Open-Label Dose-Escalation Phase I Study to Asses the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of RG2133 (2',3',5'-Tri-O-Acetyluridine) in the Treatment of Inherited Mitochondrial Diseases

Resource links provided by NLM:


Further study details as provided by Repligen Corporation:

Estimated Enrollment: 12
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   3 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria
Mitochondrial Disease
  Contacts and Locations
No Contacts or Locations Provided
  More Information

ClinicalTrials.gov Identifier: NCT00060515     History of Changes
Other Study ID Numbers: RG2133-01
First Submitted: May 7, 2003
First Posted: May 8, 2003
Last Update Posted: December 9, 2005
Last Verified: August 2005

Additional relevant MeSH terms:
Mitochondrial Diseases
Metabolic Diseases