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Hypersensitivity Reaction to Vitrase (Ovine Hyaluronidase)

2014-07-24 14:27:24 | BioPortfolio

Summary

The objective of this study was to rule out a greater than 10% incidence of hypersensitivity to Vitrase following a single intradermal injection of 3 USP units Vitrase. Less than or equal to 10% hypersensitivity response was considered acceptable.

Study Design

Observational Model: Defined Population, Time Perspective: Cross-Sectional, Time Perspective: Prospective

Conditions

Drug Hypersensitivity

Intervention

Vitrase (ovine hyaluronidase); Sterile saline

Location

Solano Clinical Research (A Division of Dow Pharmaceutical Sciences)
Davis
California
United States
95616

Status

Completed

Source

ISTA Pharmaceuticals

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-24T14:27:24-0400

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