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The ILLUMERA Study

Illumera logo

Living with Lewy body dementia (LBD) can be overwhelming, not just because of problems with memory or movement, but also because of symptoms like seeing or hearing things that are not really there (hallucinations) or developing strong beliefs that are not true (delusions). Hallucinations and delusions are common symptoms of Lewy body dementia and are called LBD psychosis. Psychosis is a medical condition where someone may lose touch with reality, but it does not mean the individual is violent or unsafe.

What is the study about?

The purpose of this research study is to evaluate an investigational drug for LBD psychosis that may help reduce these symptoms and allow researchers to learn more and move us closer to better treatment options.

What is involved?

If you decide to learn more about this study and consider volunteering, here is what you can expect:

  • Screening period (up to 30 days): This period is used to determine eligibility for the study and will involve one clinic visit.
  • Treatment period (6 weeks): Participants are randomly assigned to receive one of two different doses of the study medication or a placebo. While taking the study drug or placebo, participants will visit the clinic 5 times over 6 weeks.
  • Assessments: Participants will be assessed for psychotic symptoms using standard clinical tools to assess presence and severity. The eligible participant will also undergo medical exams and lab testing throughout the trial.
  • Care partner role: A care partner of yours will participate with you, including attending visits, helping with assessments, and remaining closely involved throughout the study.
  • Costs covered: There is no cost to participate. All study visits, exams, and the assigned study drug are provided at no charge. Reimbursement for study-related expenses may also be available.
  • Next steps: After the 6-week study, participants may be able to join an extension study where everyone receives the active medication.

Study doctors and staff will closely monitor participants and answer any questions that may arise throughout this research project.

Who can participate?

A person may be able to participate in this study if they:

  • Are 55 to 84 years old
  • Have been diagnosed with Lewy body dementia (either dementia with Lewy bodies or Parkinson’s disease dementia)
  • Have experienced hallucinations and/or delusions for at least 2 months
  • Have a care partner who can come to visits and help with study participation

Study Sites

StateCitySite NameContact
CaliforniaOrangeATP Clinical Research, Inc.Sarah Perkins
Study Coordinator
[email protected]
949.354.5353
FloridaAventuraHumanity Clinical ResearchGianluca Esposito
Study Coordinator
[email protected]
305.705.3441
FloridaBoca RatonParkinson’s Disease and Movement Disorders CenterKarla Arias
Study Coordinator
[email protected]
561.392.1818
FloridaClermontK2 Medical Research Winter GardenMelisa Nicolas
Study Coordinator
[email protected]
321.500.5252
FloridaHomesteadHomestead Associates in ResearchMabel Perez
Study Coordinator
[email protected]
305.246.0873
FloridaLady LakeK2 Medical Research The VillagesTakashi Sado
Study Coordinator
[email protected]
352.500.5252
FloridaMaitlandNeurology Associates, P.A.Christina Isbell
Study Coordinator
[email protected]
407.647.5996
FloridaMiamiPremier Clinical Research Institute, IncAna Mendendez
Study Coordinator
[email protected]
305.392.0279
FloridaMiamiMediClear Medical & Research CenterKatiuska Leal
Primary Study Coordinator
[email protected]
768.615.2861
FloridaMiamiAdvanced Clinical Research NetworkYaima Valdes
Study Coordinator
[email protected]
305.681.3111
FloridaWest Palm BeachHealth Synergy Clinical Research, LLCTara Thomas
Primary Study Coordinator
[email protected]
561.473.3472
HawaiiHonoluluHawaii Pacific NeuroscienceBaylee Valenzuela
Primary Study Coordinator
[email protected]
808.564.6141
KansasKansas CityUniversity of Kansas Medical Center Research Institute, Inc.Kim Lee
Primary Study Coordinator
[email protected]
913.588.0013
New YorkCommackParkinson’s Disease and Movement Disorders Center of Boca Raton dba Parkinson’s Research Center of American-Long IslandKayla Manel
Primary Study Coordinator
[email protected]
631.462.7774
North CarolinaChapel HillUNC HospitalsMary Sutton
Study Coordinator
[email protected]
919.962.8805
OhioColumbusThe Ohio State UniversityKristina Rawson
Study Coordinator
[email protected]
614.685.6772
OhioLakewoodCleveland Clinic FoundationElizabeth Irwin
Study Coordinator
[email protected]
216.237.6411
OklahomaTulsaThe Movement Disorder Clinic of OKElise Gibson
Study Coordinator
[email protected]
918.392.4530
TexasCypressHorizon Clinical Research GroupShatabdi Satpathi
Study Coordinator
[email protected]
949.491.0710
TexasSan AntonioUniversity of Texas Health Science Center San AntonioCarolyn Paiz
Primary Study Coordinator
[email protected]
210.450.8830
TexasStaffordR and H Clinical ResearchElizabeth Montoya
Study Coordinator
[email protected]
832.886.3888
VirginiaHenricoVirginia Commonwealth UniversityKara McHaney
Study Coordinator
[email protected]
804.828.4788
WashingtonKirklandEvergreen HealthUmarkar Pranjali
Study Coordinator
[email protected]
425.899.5361

Study Funder/Sponsor

This study is funded and sponsored by Acadia Pharmaceuticals, Inc.

For more information visit Illumera Study or contact:

Primary Contact

Name: Kristin Kidd

Phone Number: (434) 841-3162

Email: [email protected]

Alternate Contact

Name: Becky Howell

Phone Number: (848) 702-1886

Email: [email protected]

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