The INSYTE (Management of Parkinson's Disease Psychosis in Actual Practice) Study

  • participants needed
  • sponsor
    ACADIA Pharmaceuticals Inc.
Updated on 16 March 2020


To examine the current disease progression of PDP, the clinical, economic, and humanistic impact of anti-psychotic therapy in the management of the condition in real-world settings, and the burden of the condition on patients and their caregivers


Condition Parkinson's disease, Parkinson's disease
Treatment Real-world, non-interventional
Clinical Study IdentifierNCT03152292
SponsorACADIA Pharmaceuticals Inc.
Last Modified on16 March 2020


Yes No Not Sure

Inclusion Criteria

Adult males and females 18 with PDP
Ability to understand and read English
Patient is willing and able to sign an Informed Consent Form (ICF), or have a Legally Authorized Representative willing and able to consent on the patient's behalf
Possess the symptoms commonly associated with PDP, e.g., hallucinations and delusions that cannot be reasonably attributed to other causes

Exclusion Criteria

Patient is unwilling to participate in the non-interventional study
Patient is currently participating in or is planning to participate in an investigational clinical trial
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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