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Bioequivalency Study of Protriptyline 10 mg Tablets Under Fasted Conditions

A Single Dose, 2-Period, 2-way Crossover Bioequivalency Study of Protriptyline Tablets 10 mg Under Fasted Conditions

NCT00754962•Roxane Laboratories

View on ClinicalTrials.gov

Summary

The objective of this study was to prove the bioequivalence of Protriptyline 10 mg tablets under fasted conditions

Eligibility

Age

18 - 45 years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening

Exclusion Criteria

•Positive test for HIV, Hepatitis B, or Hepatitis C.
•Treatment with known enzyme altering drugs.
•History of allergic or adverse response to Protriptyline or any comparable or similar product.

Locations (1)

Advanced Biomedical Research

Hackensack, New Jersey, United States

Key Dates

Start Date

December 1, 2006

Primary Completion Date

January 1, 2007

Completion Date

January 1, 2007

Last Updated

January 23, 2018

Enrollment

ACTUAL participants

Conditions

Depression

Interventions

protriptyline

DRUG

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 23, 2018Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Bioequivalency Study of Protriptyline 10 mg Tablets Under Fasted Conditions

Inclusion Criteria

Exclusion Criteria

ACT Together: Implementing a Web-Based Program With Brief Coaching for Parents of Children With Disabilities in Pediatric Outpatient Clinics

A Study of a Deuterated Psilocin Analog (CYB003) in Humans With Major Depressive Disorder

Readiness and Progress in Emotion Regulation Therapy

Psilocybin for Depression in People With Mild Cognitive Impairment or Early Alzheimer's Disease

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