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Bioequivalency Study of Naratriptan Hydrochloride 2.5 mg Under Fasted Conditions

2014-07-23 21:08:21 | BioPortfolio

Summary

The objective of this study was to prove the bioequivalence of Naratriptan Hydrochloride Tablet under fasted conditions.

Study Design

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

Conditions

Migraine

Intervention

naratriptan hydrochloride

Location

Charles River Northwest Kinetics
Tacoma
Washington
United States
98418

Status

Completed

Source

Roxane Laboratories

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-23T21:08:21-0400

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