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Study of the Tolerability of Different SAR153191 Drug Products, That Differ With Respect to Manufacturing Processes and Formulation, at Different Concentrations and Doses in Healthy Male Subjects

Rheumatoid Arthritis Clinical Trial

Official title:
Randomized, Double-blind, Single Subcutaneous Dose, Parallel Design Study of the Tolerability of Different SAR153191 Drug Products, That Differ With Respect to Manufacturing Processes and Formulation, at Different Concentrations and Doses, in Healthy Male Subjects

Clinical Trial Summary

Primary objective: To determine the tolerability of different SAR153191 drug products that differ with respect to manufacturing processes and formulation, at different concentrations and doses, after administration of single subcutaneous doses to healthy male subjects. Secondary objectives: To determine the pharmacokinetic profile of the different SAR153191 drug products administered subcutaneously. To assess the safety of the different SAR153191 drug products administered subcutaneously.

Clinical Trial Description

Up to 35 Days ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06159452
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 1
Start date July 9, 2010
Completion date December 21, 2010
View Details
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