Evaluating a New Iloperidone Titration Scheme in Bipolar I Disorder or Schizophrenia
Completed · Phase 1
Conditions studied: Bipolar I Disorder, Schizophrenia
In brief
This is a single-center open-label study to be conducted in the United States in subjects with bipolar I disorder or schizophrenia.
Key facts
- Study ID
- NCT04127058
- Run by
- Vanda Pharmaceuticals
- People needed
- 12
- Starts
- 2019-10-07
- Expected to finish
- 2019-11-27
- Last updated by the study team
- 2020-04-13
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female patients 18 to 65 years of age (inclusive)
- Diagnosed with either schizophrenia or bipolar I disorder, manic or mixed type as per DSM-V criteria
- Symptomatically stable within the past two months
You may not qualify if…
- Exposure to any investigational medication, including placebo, in the past 60 days
- Non-response to clozapine
Where it is running
- Vanda Investigational Site — Marlton, New Jersey, United States
Full record on ClinicalTrials.gov
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