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Drug Use Investigation Of Effexor (SECONDARY DATA COLLECTION STUDY; SAFETY AND EFFICACY OF EFFEXOR.UNDER JAPANESE MEDICAL PRACTICE)

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Viatris

Status

Completed

Conditions

Depression/Depressed State

Treatments

Drug: venlafaxine

Study type

Observational

Funder types

Industry

Identifiers

NCT02958527
B2411278

Details and patient eligibility

About

SECONDARY DATA COLLECTION STUDY; SAFETY AND EFFICACY OF EFFEXOR.UNDER JAPANESE MEDICAL PRACTICE

Full description

This study will be conducted under the central registration system until the number of subjects who meet the conditions for registration reaches the target number of subjects. 12 weeks from the start date. The patients who completed the 12-week treatment with this product will be observed up until Week 52.

Enrollment

1,408 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with no experience of using this product who will be administered this product for the first time

Exclusion criteria

  • Exclusion criteria are not provided in this study

Trial design

1,408 participants in 1 patient group

venlafaxine
Description:
Patients with no experience of using time Effexor(venlafaxine) who will be administered time Effexor(venlafaxine)for the first
Treatment:
Drug: venlafaxine

Trial documents
2

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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