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A Clinical Trial of CoFactor Formulations and Leucovorin Administered Intravenously in Healthy, Adult Subjects.

Healthy Adults Clinical Trial

Official title:
A Single Dose, Within Subject, 3 Period, Pharmacokinetic Bridging Study of CoFactor Formulations and of Leucovorin Administered Intravenously in Healthy, Adult Subjects.

Clinical Trial Summary

The purpose of this study is to determine the safety and tolerability of CoFactor in healthy subjects.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00663481
Study type Interventional
Source Mast Therapeutics, Inc.
Contact
Status Completed
Phase Phase 1
Start date April 2008
Completion date May 2008
View Details
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