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Expanded Access of Pimavanserin for Patients With PD Psychosis

Primary Purpose

Parkinson's Disease Psychosis

Status
Approved for marketing
Phase
Locations
Study Type
Expanded Access
Intervention
Pimavanserin tartrate
Sponsored by
ACADIA Pharmaceuticals Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an expanded access trial for Parkinson's Disease Psychosis

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All Sexes

Inclusion Criteria:

  1. Patient meets one of the following criteria:

    1. Patient has participated in a previous study of pimavanserin for Parkinson's disease psychosis (PDP)
    2. New ("De novo") patients
  2. A clinical diagnosis of Parkinson's disease with a minimum duration of 1 year
  3. Female patients must be of non-childbearing potential
  4. Psychotic symptoms must have developed after Parkinson's disease diagnosis was established
  5. Patient that has received stereotaxic surgery for subthalamic nucleus deep brain stimulation must be at least 6 months post-surgery and the stimulator settings must have been stable for at least 1 month prior to Study Day 1 (Baseline) and must remain stable during the trial
  6. The patient or Legally Authorized Representative (LAR) is willing and able to provide consent
  7. The patient or LAR is willing and able to adequately communicate in English.

Exclusion Criteria:

  1. Patient has a history of significant psychotic disorders prior to or concomitantly with the diagnosis of Parkinson's disease including, but not limited to, schizophrenia or bipolar disorder
  2. Patient has had dementia prior to or concurrently with their diagnosis of Parkinson's disease that may be inconsistent with a Parkinson's diagnosis
  3. Patient has current evidence of a serious and/or unstable cardiovascular, respiratory, gastrointestinal, renal, hematologic, or other medical disorder, including cancer or malignancies, which would affect the patient's ability to participate in the program
  4. Patient has had a myocardial infarction in last six months
  5. Patient has any surgery planned during the screening, treatment, or follow-up periods

Patients will be evaluated at screening to ensure that all criteria for study participation are met. These evaluations will include specific measures of psychosis severity, delirium, dementia, cardiovascular condition, and pregnancy status. Patients may be excluded from the study based on these assessments (and specifically if it is determined that their baseline health and psychiatric condition do not meet all pre-specified entry criteria).

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    May 3, 2016
    Last Updated
    April 17, 2017
    Sponsor
    ACADIA Pharmaceuticals Inc.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02762591
    Brief Title
    Expanded Access of Pimavanserin for Patients With PD Psychosis
    Official Title
    Expanded Access Program of Pimavanserin in Patients With Parkinson's Disease Psychosis
    Study Type
    Expanded Access

    2. Study Status

    Record Verification Date
    April 2017
    Overall Recruitment Status
    Approved for marketing
    Study Start Date
    undefined (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    ACADIA Pharmaceuticals Inc.

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this program is to provide patients with PDP access to pimavanserin until the product receives marketing approval from the FDA and is commercially available.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Parkinson's Disease Psychosis

    7. Study Design

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    Pimavanserin tartrate
    Intervention Description
    Pimavanserin tartrate 40 mg, tablet, taken as two 20 mg tablets, once daily by mouth

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Eligibility Criteria
    Inclusion Criteria: Patient meets one of the following criteria: Patient has participated in a previous study of pimavanserin for Parkinson's disease psychosis (PDP) New ("De novo") patients A clinical diagnosis of Parkinson's disease with a minimum duration of 1 year Female patients must be of non-childbearing potential Psychotic symptoms must have developed after Parkinson's disease diagnosis was established Patient that has received stereotaxic surgery for subthalamic nucleus deep brain stimulation must be at least 6 months post-surgery and the stimulator settings must have been stable for at least 1 month prior to Study Day 1 (Baseline) and must remain stable during the trial The patient or Legally Authorized Representative (LAR) is willing and able to provide consent The patient or LAR is willing and able to adequately communicate in English. Exclusion Criteria: Patient has a history of significant psychotic disorders prior to or concomitantly with the diagnosis of Parkinson's disease including, but not limited to, schizophrenia or bipolar disorder Patient has had dementia prior to or concurrently with their diagnosis of Parkinson's disease that may be inconsistent with a Parkinson's diagnosis Patient has current evidence of a serious and/or unstable cardiovascular, respiratory, gastrointestinal, renal, hematologic, or other medical disorder, including cancer or malignancies, which would affect the patient's ability to participate in the program Patient has had a myocardial infarction in last six months Patient has any surgery planned during the screening, treatment, or follow-up periods Patients will be evaluated at screening to ensure that all criteria for study participation are met. These evaluations will include specific measures of psychosis severity, delirium, dementia, cardiovascular condition, and pregnancy status. Patients may be excluded from the study based on these assessments (and specifically if it is determined that their baseline health and psychiatric condition do not meet all pre-specified entry criteria).

    12. IPD Sharing Statement

    Learn more about this trial

    Expanded Access of Pimavanserin for Patients With PD Psychosis

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