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Trials / Withdrawn

WithdrawnNCT01046162

A Study Of Two Oral Preparations Of 2 Mg Alprazolam In Healthy Volunteers Under Fasting Conditions

An Open Label,Crossover,Randomized Study Of Two Periods,Two Treatments,Two Sequences, And A Single Dose Of Two Oral Drug Products Of Alprazolam 2mg (Tafil (r), Product Of Pharmacia& Upjohn S.a De C.v Vs Xanax 2mg, Product Of Pfizer Pharmaceuticals Llc) In Healthy Volunteers In Fasting Conditions

Status
Withdrawn
Phase
Phase 1
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare bioavailability between formulations of alprazolam in tablets to determine their bioequivalence in terms of rate and magnitude of absorption.

Conditions

Interventions

TypeNameDescription
DRUGAlprazolamSingle tablet
DRUGAlprazolamSingle tablet

Timeline

Start date
2010-07-15
Primary completion
2010-07-22
Completion
2010-07-22
First posted
2010-01-11
Last updated
2021-01-28

Source: ClinicalTrials.gov record NCT01046162. Inclusion in this directory is not an endorsement.

A Study Of Two Oral Preparations Of 2 Mg Alprazolam In Healthy Volunteers Under Fasting Conditions (NCT01046162) · Clinical Trials Directory