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CompletedNCT00868699

Lurasidone alone for depression in bipolarity

About this titleRead the official source — NCT00868699

Researchers compared lurasidone and placebo to find out how the approaches affected depression symptoms in people with bipolarity type I during a depressive episode.

Medication studyAges 18–75Multiple countries
The study in practice

Understand this study

What did researchers investigate?

Researchers compared lurasidone and placebo to find out how the approaches affected depression symptoms in people with bipolarity type I during a depressive episode.

Who was this study for?

This study was for people with bipolarity. Listed age limits: 18 years to 75 years. Other eligibility criteria applied.

Listed locations
Escondido and 54 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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Study clarity

Study information

Study start dateApril 2009
Recruitment status
Completed
Enrollment listed in the registry
505
Sponsor
Sumitomo Pharma America, Inc.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States, France, Czechia, ...
Age range
From 18 Years to 75 Years
Official registry ID
NCT00868699
Official title
Show the full official title

A Randomized, 6-Week, Double-Blind, Placebo-Controlled, Fixed-Flexible Dose, Parallel-Group Study of Lurasidone for the Treatment of Bipolar I Depression

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Recruitment & locations

Completed

Escondido, United States · Garden Grove, United States · Oceanside, United States

49 more locations
  • Orange, United States
  • Pico Rivera, United States
  • San Diego, United States
  • Aurora, United States
  • Bradenton, United States
  • Maitland, United States
  • Tampa, United States
  • West Palm Beach, United States
  • Oak Brook, United States
  • Lake Charles, United States
  • Baltimore, United States
  • Albuquerque, United States
  • Cedarhurst, United States
  • Rochester, United States
  • Raleigh, United States
  • Cleveland, United States
  • Philadelphia, United States
  • Austin, United States
  • Kolejni 429-5, Czechia
  • Brno - Mesto, Czechia
  • Litoměřice, Czechia
  • Prague, Czechia
  • Nîmes, France
  • Orvault, France
  • Tirupati, India
  • Vijaywada, India
  • Ahmedabad, India
  • Bangalore, India
  • Nashik, India
  • Jaipur, India
  • Lucknow, India
  • Bucdresti, Romania
  • Bucharest, Romania
  • Cluj-Napoca, Romania
  • Craiova, Romania
  • Oradea, Romania
  • Saint Petersburg, Russia
  • Cape Town, W. Cape, South Africa
  • Paarl, W. Cape, South Africa
  • Port Elizabeth, E. Cape, South Africa
  • Pretoria, Gauteng, South Africa
  • Vereeniging, Free State, South Africa
  • Donetsk, Ukraine
  • Odesa, Ukraine
  • Poltava, Ukraine
  • Simferopol, Ukraine
  • Vinnitsia, Ukraine
  • Czechia
  • Russia
FAQ

Questions about this study

What did researchers investigate?

Researchers compared lurasidone and placebo to find out how the approaches affected depression symptoms in people with bipolarity type I during a depressive episode.

Who is behind this study?

The study sponsor is Sumitomo Pharma America, Inc., a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including lurasidone and Placebo.

Who was this study for?

This study was for people with bipolarity. Listed age limits: 18 years to 75 years. Other eligibility criteria applied.

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