WHO ICTRP trial

A global study to see how safe, effective and well tolerated a capsule…

EUCTR2010-018860-17-DE · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2010-018860-17-DE
Public title A global study to see how safe, effective and well tolerated a capsule containing Aripiprazole and Escitalopram is in people with depression.
Scientific title A Multicenter, 52-week, Open-label Study to Assess the Safety and Tolerability of an Oral Aripiprazole/Escitalopram Combination Therapy in Patients with Major Depressive Disorder - ACES 257
Primary sponsor Otsuka Pharmaceutical Development & Commercialization, Inc.
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Countries United States;Serbia;Philippines;Estonia;Taiwan;Slovakia;Spain;Ukraine;Russian Federation;Italy;India;France;Malaysia;Australia;South Africa;Korea, Republic…
Conditions Major Depressive Disorder (MDD) MedDRA version: 14.0 Level: LLT Classification code 10025454 Term: Major depressive disorder, recurrent episode System Organ Class: 10037175 - Psychiatric disorders ;Therapeutic area: Psychiatry and…
Interventions Product Name: Aripiprazole/Escitalopram 3-10 mg Combination Capsule Product Code: OPC-14597 Pharmaceutical Form: Capsule INN or Proposed INN: ARIPIPRAZOLE CAS Number: 129722-12-9 Concentration unit: mg milligram(s) Concentration type: equal…
Registration date Sep 23, 2010
Target size 1500
Secondary IDs 31-08-257
Registry page clinicaltrialsregister.eu

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