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Pimavanserin vs. Quetiapine for the Treatment Parkinson's Psychosis (C-SAPP)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT04373317
Recruitment Status : Not yet recruiting
First Posted : May 4, 2020
Last Update Posted : April 9, 2021
Information provided by (Responsible Party):
VA Office of Research and Development

Brief Summary:

Patients with Parkinson's disease (PD) sometimes experience symptoms affecting their movement, such as slowness, tremor, stiffness, and balance or walking problems. Many patients also have other symptoms not related to movement, called non-motor symptoms, which may affect one's mood or emotions, memory or thinking, or cause one to see or hear things that aren't real (hallucinations) or believe things that aren't true (delusions). Hallucinations or delusions, together called psychosis, occur in up to 60% of PD patients at some point in time. Parkinson's disease psychosis can sometimes be associated with decreased quality of life, increased nursing home placement, increased rate of death, and greater caregiver burden. There are approximately 50,000 Veterans with Parkinson's disease receiving care in the VA, and up to 30,000 (60%) of them will experience psychosis at some point in time.

Quetiapine is an antipsychotic drug approved by the Food and Drug Administration (FDA) that is the most commonly used medication to treat PD psychosis, but more studies are needed to determine if it works for this condition and is also well tolerated and safe. Pimavanserin is a newer antipsychotic drug approved by the Food and Drug Administration (FDA) specifically to treat PD psychosis, but more studies are needed to determine if it works and its safety.

The purpose of this research is to gather additional information on the safety and effectiveness of both Quetiapine and Pimavanserin. By doing this study, the investigators hope to learn which of these medications is the most effective course of treatment for people with PD psychosis. Your individual participation in this research will last approximately 54 weeks.

Condition or disease Intervention/treatment Phase
Parkinson's Disease Psychosis Drug: Pimavanserin Drug: Quetiapine Phase 4

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 358 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Two active treatments will be administered in this RCT, with 1:1 treatment assignment to either quetiapine or pimavanserin. Both active treatments are FDA-approved antipsychotics.
Masking: Triple (Participant, Care Provider, Investigator)
Masking Description: In order to facilitate titrations, study drug will be provided in blister cards with a sufficient number of over-encapsulated drug to bridge participants to their next titration step. Each blister card will contain a one-week supply of study drug. Because dosing will be nightly, and the study will use a combination of quetiapine strengths for all protocol-specified quetiapine doses, participants in both treatment groups will take two identical capsules both of which containing the protocol-specified nightly dose. For example, if a participant is randomized to quetiapine and is up-titrated from 50 to 100 mg ER, this participant will take 2 identical capsules, each containing 50 mg of ER quetiapine. Similarly, participants randomized to pimavanserin will take two capsules every night, one containing a placebo capsule, and the other containing 34 mg of pimavanserin.
Primary Purpose: Treatment
Official Title: CSP #2015 - Multicenter, Randomized, Double-blind Comparator Study of Antipsychotics Pimavanserin and Quetiapine for Parkinson''s Disease Psychosis (C-SAPP)
Estimated Study Start Date : October 1, 2021
Estimated Primary Completion Date : October 1, 2024
Estimated Study Completion Date : January 1, 2025

Arm Intervention/treatment
Active Comparator: Pimavanserin 34mg
All participants assigned to pimavanserin will receive the FDA-approved dose of 34mg (equivalent to 40 mg pimavanserin tartrate) daily without titration; however, because pimavanserin is blinded to quetiapine, participants will undergo sham titration based on tolerability.
Drug: Pimavanserin
Pimavanserin is a new antipsychotic agent, and pure 5HT-2A inverse agonist, that was approved by the FDA recently (2016) for the treatment of PDP.

Active Comparator: Quetiapine

Quetiapine extended release will be titrated as shown in the following table. During the 8-week treatment phase, there is a maximum of 6 weeks for titration.

Titration Schedule

Visit/call Quetiapine Dose (Flexible)Quetiapine Notes Baseline visit (Visit 00)25 mg IR QHSAll participants must be up-titrated to at least 50 mg/day at week 1 Week 1 call (Visit 01)50 mg XR QHSUp-titration Week 3 visit (Visit 03)100 mg XR QHS (requiring two 50-mg quetiapine XR capsules)Up- or down-titration as appropriate based on psychosis symptoms and tolerability Week 5 visit (Visit 05)150 mg quetiapine XR QHSUp- or down-titration as appropriate based on psychosis symptoms and tolerability Week 6 call (Visit 06)200 mg quetiapine XR QHSUp- or down-titration as appropriate based on psychosis symptoms and tolerability

Drug: Quetiapine
Quetiapine, which is a mixed serotonin and dopamine receptor antagonist but also binds to many other brain receptors (e.g., adrenergic, cholinergic, histaminergic receptors), is by far the most commonly used AP for PDP (at least 70% of prescriptions) and does not require special monitoring.

Primary Outcome Measures :
  1. CGI-I Psychosis [ Time Frame: 8 Weeks ]
    CGI-I (for psychosis). The Clinical Global Impressions (CGI) scale is a brief, well-established research rating tool used to quantify and track patient progress and treatment response over time. It was originally developed to be used in clinical trials on mental health to provide an assessment of the clinician's view of the patient's global functioning over time with a study medication. The CGI comprises two measures, one of which is Improvement (CGI-I) from the initiation of treatment. It is scored 1 to 7. The CGI-I is used to assess how much the patient's illness has improved or worsened relative to baseline when the intervention was started (1-Very much improved, 2-Much improved, 3-Minimally improved, 4-No change, 5-Minimally worse, 6-Much worse, 7-Very much worse). The CGI-I can also be used to assess specific domains, including psychosis (this study's primary outcome) and parkinsonism (a secondary outcome).

Secondary Outcome Measures :
  1. SAPS-PD [ Time Frame: 8 Weeks ]
    The primary assessment of change in psychosis severity will be the score on the 9-item Parkinson's disease-adapted Scale for Assessment of Positive Symptoms (SAPS-PD).59 The SAPS-PD scale is designed to assess positive symptoms, including hallucinations, delusions, bizarre behavior, and positive formal thought disorder. A standard clinical interview with probing questions is used to evaluate the participant's symptoms. Items include: 1) Auditory Hallucinations; 2) Voices Conversing; 3) Somatic or Tactile Hallucinations; 4) Visual Hallucinations; 5) Global Rating of Severity of Hallucinations; 6) Persecutory Delusions; 7) Delusions of Jealousy; 8) Ideas and Delusions of Reference; and 9) Global Rating of Severity of Delusions. Each item is given a score ranging 0 to 5 (0-None, 1-Questionable, 2-Mild, 3-Moderate, 4-Marked, 5-Severe). Thus, total scores for SAPS-PD ranges 0-45.

  2. MDS-UPDRS III [ Time Frame: 8 Weeks ]
    The Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part III (Motor Examination; MDS-UPDRS III) has 33 scores across 18 items (each score 0-4, range of total score 0-132, with higher scores indicating more severe motor symptoms) is completed by a trained rater during an examination of the patient, and is the most commonly-used assessment of parkinsonism in clinical trials. MDS-UPDRS III includes ratings for tremor, slowness (bradykinesia), stiffness (rigidity), and gait/balance. The MDS-UPDRS III will be administered to all participants (quetiapine or pimavanserin) at each in-person visit (baseline, 3 weeks, 5 weeks, and 8 weeks). Administration will also occur at weeks 10, 13, 15, and 18 for non-responders at week 8, and months 3, 6, 9, and 12 for responders at week 8. The CGI-I for parkinsonism will similarly be assessed at these study visits to address this secondary outcome.

  3. Zarit Caregiver Burden Scale [ Time Frame: 8 Weeks ]
    The Zarit Burden Interview (ZBI) is a 22-item self-report inventory that examines burden associated with functional/behavioral impairments and the home care situation.64 It was originally developed to measure subjective burden among caregivers of adults with dementia. The items are worded subjectively, focusing on the affective response of the caregiver. Each question is scored on a 5-point Likert scale ranging from 0 to 4 (0-Never, 1-Rarely, 2-Sometimes, 3-Frequently, 4-Nearly always). The ZBI total score ranges from 0 (low burden) to 88 (high burden), the sum of the scores from all 22 questions. Interpretation of the total scores is typically: 1) 0-21 little or no burden; 2) 21-40 mild to moderate burden; 3) 41-60 moderate to severe burden; and 4) 61-88 severe burden. The ZBI will be administered to all participants' informed other at baseline and treatment phase visits of Weeks 5 and 8.

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   40 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Veteran
  • Diagnosis of idiopathic PD for 2 or more years
  • Psychosis [with Neuropsychiatric Inventory (NPI) hallucinations (B) or delusions (A) score 4 or greater]
  • Stable dose of PD medications for at least 1 month If on an acetylcholinesterase inhibitor (AChEI) initially prescribed at least 3 months prior and stable dose (no dose or medication change) for past month Informed other must provide informed consent and agree to attend all study visits. The informed other must be at least 18 years of age and have regular in-person contact with the patient (at least 5 days per week, and at least 4 hours per day that is spent with patient) English-speaking

Exclusion Criteria:

  • Psychosis symptoms severe enough to preclude enrollment in a clinical trial and require prompt clinical care instead
  • Treatment with an antipsychotic, including pimavanserin in the past year, except quetiapine <50 mg/day which has been discontinued for at least 1 month prior to study enrollment
  • Deep brain stimulation (DBS) surgery occurring within 6 months prior or having unstable stimulator settings in the previous month
  • History of a psychotic disorder prior to PD, including schizophrenia and bipolar disorder
  • Suspected atypical parkinsonian disorder or dementia with Lewy bodies (DLB)
  • Psychosis secondary to other toxic or metabolic disorder
  • Congestive heart failure
  • History of stroke within the last 6 months
  • History of myocardial infarction within the last 6 months
  • History of long QT syndrome or prolonged QTc [>450ms in men, >470ms in women] at screening/baseline (or baseline, if applicable)
  • Current uncontrolled serious medical illness
  • Clinically significant hepatic impairment or severe renal impairment (eGFR <30 mL/min)
  • Currently taking medications that are significant CYP3A4 inhibitors or inducers
  • Comorbid medical condition determined too severe by SI to allow participation in clinical trial
  • Failure to tolerate quetiapine or pimavanserin previously
  • Moderate to severe PD dementia (MoCA score <13)
  • Currently enrolled in another therapeutic or interventional study
  • Nursing home placement at baseline or planned placement during the study
  • Active suicidality
  • Pregnancy/Pregnant, or a female of child-bearing potential who is unwilling to use a reliable form of contraception

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT04373317

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Contact: Daniel Weintraub, MD (215) 823-5800 ext 5934
Contact: John E Duda, MD (215) 823-5934

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Sponsors and Collaborators
VA Office of Research and Development
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Study Chair: Daniel Weintraub, MD Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
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Responsible Party: VA Office of Research and Development Identifier: NCT04373317    
Other Study ID Numbers: 2015
First Posted: May 4, 2020    Key Record Dates
Last Update Posted: April 9, 2021
Last Verified: April 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Keywords provided by VA Office of Research and Development:
Additional relevant MeSH terms:
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Parkinson Disease
Psychotic Disorders
Mental Disorders
Parkinsonian Disorders
Basal Ganglia Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Movement Disorders
Neurodegenerative Diseases
Schizophrenia Spectrum and Other Psychotic Disorders
Quetiapine Fumarate
Antidepressive Agents
Psychotropic Drugs
Antipsychotic Agents
Tranquilizing Agents
Central Nervous System Depressants
Physiological Effects of Drugs
Antiparkinson Agents
Anti-Dyskinesia Agents
Serotonin 5-HT2 Receptor Antagonists
Serotonin Antagonists
Serotonin Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action