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NCT00775996

The Objective of This Study Was to Compare the Single-Dose Relative Bioavailability of Ranbaxy and Abbott (Tranxene® T-Tab®) 15 mg Clorazepate Dipotassium Tablets Under Fasting Conditions.

Completed NA Last updated 17 October 2008
What this trial tests

NA trial testing Clorazepate Dipotassium 15mg Tablets in Healthy in 32 participants. Completed in 1 November 2003.

Timeline
1 August 2003
Primary endpoint
1 September 2003
1 November 2003

Quick facts

Lead sponsorRanbaxy Laboratories Limited
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Enrollment32
Start date1 August 2003
Primary completion1 September 2003
Estimated completion1 November 2003
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Ranbaxy Laboratories Limited — full company profile →

Who can join

Adults 18 to 55, any sex, with Healthy. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The objective of this study was to compare the single-dose relative bioavailability of Ranbaxy and Abbott (TranxeneeT-Tab®) 15 mg clorazepate dipotassium tablets under fasting conditions.

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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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00775996.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing