Clinical Trial: Tolerability and Safety of An Infant Formula
Study Status: Completed
Recruit Status: Completed
Study Type: Interventional
Official Title: A Multicenter, Single-blind, Randomized, Phase II Study of the Tolerability and Safety of NPS-202 in Infants With Clinically Diagnosed Cow's Milk Allergy
Brief Summary: The purpose of this study is to evaluate an extensively hydrolyzed formula in infants with cow's milk allergy.
Detailed Summary:
Sponsor: Perrigo Nutritionals
Current Primary Outcome: Infant reactivity to an extensively hydrolyzed infant formula [ Time Frame: 29 days ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
Original Secondary Outcome:
Information By: Perrigo Nutritionals
Dates:
Date Received: July 7, 2009
Date Started: August 2007
Date Completion:
Last Updated: July 14, 2009
Last Verified: July 2009