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CompletedNCT01948024

Asenapine Brand and Generic Formulations Compared in Schizophrenia or Bipolarity

About this titleRead the official source — NCT01948024
Medication studyAges 18–80United States
The study in practice

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Who was this study for?

Listed age limits: 18 years to 80 years.

Listed locations
Little Rock and 6 more locationsSee all locations and recruitment
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.

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Study clarity

Study information

Study start dateJuly 2013
Recruitment status
Completed
Enrollment listed in the registry
65
Sponsor
Sun Pharmaceutical Industries Limited
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
Locations
United States
Age range
From 18 Years to 80 Years
Official registry ID
NCT01948024
Official title
Show the full official title

An Open-label, Randomized, Two Treatment, Multi-site, Multiple Dose, Steady State, Three-way, Reference-replicated Crossover, Pharmacokinetic Study to Determine the In-vivo Bioequivalence Between Asenapine 10 mg Sublingual Tablet and SAPHRIS® (Asenapine) 10 mg Sublingual Tablet

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Recruitment & locations

Completed

Little Rock · Costa Mesa · Garden Grove

4 more locations
  • Leesburg
  • Miami
  • Atlanta
  • Charlotte

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Sun Pharmaceutical Industries Limited, a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including SAPHRIS and Asenapine.

Who was this study for?

Listed age limits: 18 years to 80 years.

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