Bioequivalence of Alprazolam Sublingual vs Oral Tablets
NCT ID: NCT00860119
Last Updated: 2021-01-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
23 participants
INTERVENTIONAL
2009-08-31
2009-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Sublingual tablet
Test treatment
alprazolam sublingual tablet
1 mg alprazolam sublingual tablet, given as a single dose to each subject
Oral tablet
Reference treatment
alprazolam oral tablet
1 mg alprazolam immediate release oral tablet, given as a single dose to each subject
Interventions
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alprazolam sublingual tablet
1 mg alprazolam sublingual tablet, given as a single dose to each subject
alprazolam oral tablet
1 mg alprazolam immediate release oral tablet, given as a single dose to each subject
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* BMI 17.5 - 30.5
* Must provide informed consent
Exclusion Criteria
* Narrow angle glaucoma
* Positive drug screen
21 Years
55 Years
ALL
Yes
Sponsors
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Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Locations
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Pfizer Investigational Site
Ahmedabad, Gujarat, India
Countries
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Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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A6131017
Identifier Type: -
Identifier Source: org_study_id
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