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Last Updated: April 25, 2024

CLINICAL TRIALS PROFILE FOR TOFRANIL-PM


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All Clinical Trials for TOFRANIL-PM

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00296725 ↗ Dichotic Listening as a Predictor of Medication Response in Depression Completed New York State Psychiatric Institute Phase 1/Phase 2 1994-04-01 Depressed patients will have hearing tests and then be treated with up to three treatments (i.e., Fluoxetine, Imipramine) until remitted, to see whether test results predict specific outcomes.
NCT00404755 ↗ Dichotic Listening as a Predictor of Medication Response in Depression Completed New York State Psychiatric Institute Phase 4 2006-07-01 This study will recruit 100 depressed patients to test whether the previous finding of an association between treatment response (with treatment groups including placebo, imipramine, and fluoxetine) and preferences of hemispheric laterality in perceptual processing are also found with a different type of commonly used anti-depressant, bupropion.
NCT00946764 ↗ To Demonstrate the Relative Bioavailability of Sandoz Inc. and Tyco Healthcare (Tofranil) 50 mg Imipramine Hydrochloride Tablets In Healthy Adults Volunteers Under Fasting Conditions Completed Sandoz Phase 1 2005-07-01 To demonstrate the relative bioavailability of Sandoz Inc. and Tyco Healthcare (Tofranil) 50 mg imipramine hydrochloride tablets in healthy adult volunteers under fasting conditions.
NCT01028014 ↗ Medication Effects on Periurethral Sensation,Urethral Sphincter Activity and Pressure Flow Parameters Completed Astellas Pharma Inc N/A 2010-04-01 Lower urinary tract symptoms such as urinary leakage and overactive bladder affect millions of American women. Women may develop these problems because the innervation of the muscles of the bladder and urethra are injured. Most research on treating these problems has focused on the abnormalities of the bladder muscle, but newer studies have shown abnormalities in the innervation and muscle function of the urethra. Women with these symptoms may benefit from treatment with medications to improve their urethral function. However, to truly understand what types of medications will help women with these symptoms, the investigators wish to study how these medications affect innervation and muscle function in healthy women who do not have lower urinary tract symptoms.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for TOFRANIL-PM

Condition Name

Condition Name for TOFRANIL-PM
Intervention Trials
Dysthymia 2
Major Depression 1
Major Depressive Disorder 1
Urethral Sphincter Activity 1
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Condition MeSH

Condition MeSH for TOFRANIL-PM
Intervention Trials
Depression 4
Depressive Disorder, Major 3
Depressive Disorder 3
Dysthymic Disorder 2
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Clinical Trial Locations for TOFRANIL-PM

Trials by Country

Trials by Country for TOFRANIL-PM
Location Trials
United States 4
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Trials by US State

Trials by US State for TOFRANIL-PM
Location Trials
New York 2
Maryland 1
Alabama 1
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Clinical Trial Progress for TOFRANIL-PM

Clinical Trial Phase

Clinical Trial Phase for TOFRANIL-PM
Clinical Trial Phase Trials
Phase 4 1
Phase 1/Phase 2 1
Phase 1 1
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Clinical Trial Status

Clinical Trial Status for TOFRANIL-PM
Clinical Trial Phase Trials
Completed 4
Withdrawn 1
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Clinical Trial Sponsors for TOFRANIL-PM

Sponsor Name

Sponsor Name for TOFRANIL-PM
Sponsor Trials
New York State Psychiatric Institute 2
Sandoz 1
Astellas Pharma Inc 1
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Sponsor Type

Sponsor Type for TOFRANIL-PM
Sponsor Trials
Other 5
Industry 2
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