NCT00913237

Brief Summary

To demonstrate the relative bioavailability of Desipramine Hydrochloride 50 mg tablets.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at P25-P50 for phase_1 depression

Timeline
Completed

Started Jul 1987

Shorter than P25 for phase_1 depression

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 1987

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 1987

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 1987

Completed
21.9 years until next milestone

First Submitted

Initial submission to the registry

June 2, 2009

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 4, 2009

Completed
Last Updated

March 28, 2017

Status Verified

June 1, 2009

Enrollment Period

1 month

First QC Date

June 2, 2009

Last Update Submit

March 27, 2017

Conditions

Depression

Keywords

Antidepressant

Outcome Measures

Primary Outcomes (1)

  • Bioequivalence based on AUC and Cmax

    28 days

Study Arms (2)

1

EXPERIMENTAL

Desipramine Hydrochloride 50 mg Tablets (Cord Laboratories)

Drug: Desipramine Hydrochloride 50 mg Tablets (Cord Laboratories)

2

ACTIVE COMPARATOR

Desipramine Hydrochloride 50 mg Tablets (Merrell Dow Pharmaceuticals, Inc)

Drug: Desipramine Hydrochloride 50 mg Tablets (Merrell Dow Pharmaceuticals, Inc)

Interventions

Desipramine Hydrochloride 50 mg Tablets (Cord Laboratories)DRUG
1
Desipramine Hydrochloride 50 mg Tablets (Merrell Dow Pharmaceuticals, Inc)DRUG
2

Eligibility Criteria

Age19 Years - 50 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • No clinically significant abnormal finding on physical exam, medical history, or clinical laboratory results on screening.

You may not qualify if:

  • Positive test results for HIV or hepatitis B or C.
  • Treatment for drug or alcohol dependence.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Depression

Interventions

Desipramine

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

DibenzazepinesHeterocyclic Compounds, 3-RingHeterocyclic Compounds, Fused-RingHeterocyclic Compounds

Study Officials

  • Jules Kann, M.D.

    Biodecision Laboratories

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
INDUSTRY

Study Record Dates

First Submitted

June 2, 2009

First Posted

June 4, 2009

Study Start

July 1, 1987

Primary Completion

August 1, 1987

Study Completion

August 1, 1987

Last Updated

March 28, 2017

Record last verified: 2009-06