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

NCT ID: NCT00060515

Last Updated: 2005-08-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE1

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Brief Summary

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The objective of the study is to determine the safety and tolerability of RG2133 in patients with Mitochondrial Disease.

Detailed Description

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Conditions

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Mitochondrial Diseases

Study Design

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Allocation Method

NON_RANDOMIZED

Primary Study Purpose

TREATMENT

Interventions

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RG2133 (2',3',5'-tri-O-acetyluridine)

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

Mitochondrial Disease
Minimum Eligible Age

3 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Repligen Corporation

INDUSTRY

Sponsor Role lead

Countries

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United States

Other Identifiers

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RG2133-01

Identifier Type: -

Identifier Source: org_study_id