Efficacy and Safety of Grass Sublingual Tablet in Children and Adolescents (P05239 AM3)(COMPLETED)
Merck Sharp & Dohme Corp.
The purpose of the study is to investigate the efficacy and safety of a grass sublingual
tablet in children and adolescents with a history of grass-pollen induced
rhinoconjunctivitis with or without asthma.
Observation of Use of Claritin (Loratadine) Tablet, RediTabs, and Dry Syrup in Children (Study P05834)(COMPLETED)
Merck Sharp & Dohme Corp.
The purpose of this study is to collect information on unexpected adverse reactions (ADRs),
how often ADRs occur, and factors that can affect the safety and effectiveness of Claritin
(loratadine) when used in children. Patients will be observed while they are taking
Claritin, and ADRs and symptom scores will be recorded. At the end of treatment, improvement
in symptoms will be recorded.
Post-marketing surveys are not considered applicable clinical trials and thus the results of
this survey will not be posted at its conclusion. The results will be submitted to public
health officials as required by applicable national and international laws.
Bioequivalence Study on Loratadine Orally Disintegrating Tablets 10 mg Under Fasting Conditions
Ranbaxy Laboratories Limited
To compare the single-dose oral bioavailability of loratadine 10 mg orally disintegrating
tablets of Ohm Laboratories (a subsidiary of Ranbaxy Pharmaceuticals Inc., USA) with
Claritin® Reditabs® (containing loratadine 10 mg) of Schering-Plough Healthcare Product
Inc., USA in healthy, adult, human male subjects under fasting condition.
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