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Efficacy and Safety Study of Oral Eligen® B12 in Subjects With Low Serum Cobalamin

Vitamin B 12 Deficiency Clinical Trial

Official title:
A 60-DAY, Open-label, Randomized Study to Evaluate the Efficacy and Safety of Eligen® B12 OR Intramuscularly Administered B12 in Subjects With Low Serum Cobalamin With a 30 Day Extension to 90 Days of Dosing

Clinical Trial Summary

The purpose of this study is to compare the efficacy and safety profile of a new oral vitamin B12 formulation (Eligen® B12) with intramuscular B12 in restoring normal B12 (cobalamin) concentrations in subjects with low cobalamin levels (<350 pg/mL).

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01312831
Study type Interventional
Source Emisphere Technologies, Inc.
Contact
Status Completed
Phase N/A
Start date February 2009
Completion date December 2010
View Details
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