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CompletedNCT01357993

A Long-Term Study on Safety of JNS001 in Adults With Attention-Deficit Hyperactivity Disorder

Researchers studied JNS001, tracking side effects to assess long-term safety and tolerability in adults with ADHD.

Medication studyAges 18–65Japan
The study in practice

Understand this study

What did researchers investigate?

Researchers studied JNS001, tracking side effects to assess long-term safety and tolerability in adults with ADHD.

Who was this study for?

This study was for people with ADHD. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

Listed locations
Chiba and 28 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateMay 2011
Recruitment status
Completed
Enrollment listed in the registry
253
Sponsor
Janssen Pharmaceutical K.K.
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
Japan
Age range
From 18 Years to 65 Years
Official registry ID
NCT01357993
Official title
Show the full official title

An Open-Label, Dose-Titration, Long-Term Study to Evaluate the Safety of JNS001 in Adults With Attention-Deficit/Hyperactivity Disorder at Doses of 18 mg, 27 mg, 36 mg, 45 mg, 54 mg, 63 mg or 72 mg Per Day

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Recruitment & locations

Completed

Chiba · Chigasaki · Chiyoda City

26 more locations
  • Fuchū
  • Fukuoka
  • Fukushima
  • Hamamatsu
  • Higashiosaka
  • Ichikawa
  • Iruma
  • Isehara
  • Kashihara
  • Kishiwada
  • Kobe
  • Kumamoto
  • Kurume
  • Matsuyama
  • Nagasaki
  • Nagoya
  • Nara
  • Neyagawa
  • Osaka
  • Saitama
  • Sakai
  • Sapporo
  • Shibuya City
  • Takatsuki
  • Tokyo
  • Yokohama
FAQ

Questions about this study

What did researchers investigate?

Researchers studied JNS001, tracking side effects to assess long-term safety and tolerability in adults with ADHD.

Who is behind this study?

The study sponsor is Janssen Pharmaceutical K.K., a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including JNS001.

Who was this study for?

This study was for people with ADHD. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

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