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NCT01745601

Bioequivalence Study of Escitalopram Tablets 10 mg

Completed Phase 1 Last updated 16 June 2017
What this trial tests

Phase 1 trial testing escitalopram 10 mg in Anxiety Disorders in 26 participants. Completed in 19 May 2010.

Timeline
4 May 2010
Primary endpoint
19 May 2010
19 May 2010

Quick facts

Lead sponsorGlaxoSmithKline
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposeother
Enrollment26
Start date4 May 2010
Primary completion19 May 2010
Estimated completion19 May 2010

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

Adults 18 to 50, male only, with Anxiety Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study was to confirm if two formulations of escitalopram tablets are bioequivalent. Test product was escitalopram (10 mg; GlaxoSmithKline) and reference product Lexapro® (10 mg escitalopram; Lundbeck). The single dosage was one tablet. The study was prospective, open-label, randomized, crossover, single dose, with 02 treatments, 02 sequences and 02 periods, under fasting conditions. The population was composed of 26 healthy volunteers, male adults between 18-50 years. The comparative bioavailability of the two formulations was evaluated based in statistical comparisons of relevant pharmacokinetic parameters, obtained from data of drug concentrations in blood.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Anxiety Disorders

Currently open trials in the same condition.

Other GlaxoSmithKline trials

Trials by the same sponsor.

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Data sources for this page

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