Expanded Access of Pimavanserin for Patients With PD Psychosis

NCT02762591 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2017-04-18

No results posted yet for this study

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.

Conditions

  • Parkinson's Disease Psychosis

Interventions

DRUG

Pimavanserin tartrate

Pimavanserin tartrate 40 mg, tablet, taken as two 20 mg tablets, once daily by mouth

Sponsors & Collaborators

  • ACADIA Pharmaceuticals Inc.

    lead INDUSTRY

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02762591 on ClinicalTrials.gov