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NCT06462612CompletedPhase 3

Study of Lumateperone in the Treatment of Patients With Bipolar Mania

A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of Lumateperone in the Acute Treatment of Patients With Manic Episodes or Manic Episodes With Mixed Features Associated With Bipolar I Disorder (Bipolar Mania)

Source: ClinicalTrials.gov · Last updated 24 Jul 2026

Brief summary (registry, in English)

This is a multicenter, randomized, double-blind, placebo-controlled, study in the acute treatment of patients with a diagnosis of bipolar I disorder with manic episodes or manic episodes with mixed features (bipolar mania), with or without psychotic symptoms, according to criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM 5).

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
351 (actual)
First submitted
12 Jun 2024
Start date
17 Jul 2024
Primary completion date
15 May 2026
Lead sponsor
Intra-Cellular Therapies, Inc.
NCT number
NCT06462612

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 351
  • From 17 Jul 2024 to the primary completion date, 15 May 2026
  • 31 sites in 4 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • In the opinion of the Investigator, the patient has a significant risk for suicidal behavior during the course of his/her participation in the study or
    • At Screening, the patient scores "yes" on Items 4 or 5 in the Suicidal Ideation section of the Columbia-Suicide Severity Rating Scale (C-SSRS) within 6 months prior to Screening; or
    • At Screening, the patient has had 1 or more suicidal attempts within 2 years prior to Screening; or
    • At Baseline, the patient scores "yes" on Items 4 or 5 in the Suicidal Ideation section of the C-SSRS since the Screening Visit; or
    • At Screening or Baseline, scores ≥ 4 on Item 10 (suicidal thoughts) on the rater administered Montgomery-Åsberg Depression Rating Scale (MADRS); or
    • Considered to be an imminent danger to himself/herself or others.

Other illness

  • Has a current primary DSM 5 psychiatric diagnosis other than bipolar disorder. These include:
    • Schizophrenia, schizoaffective disorder, or other psychotic disorders;
    • Dementia or other cognitive disorders;
    • Intellectual disability;
    • Moderate or severe substance use disorder (excluding for nicotine);

Other

  • Experiencing first manic episode;

Who the study is looking for

  • Able to provide written informed consent before the initiation of any study specific procedures;
  • Male or female inpatient, between the ages of 18 and 75 years, inclusive;
  • Meets the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM 5) criteria for bipolar I disorder with a current episode of mania or mania with mixed features with or without psychotic symptoms, as confirmed by a trained and Sponsor-approved rater using the modified Structured Clinical Interview for DSM-5, Clinical Trials Version (SCID-5-CT);
  • YMRS total score ≥ 20 and a score of at least 4 on two of the following YMRS items: irritability, speech, content, and disruptive/aggressive behavior at Screening and Baseline;
  • Hospitalized voluntarily before Screening or admitted to inpatient unit at Visit 1 with a primary diagnosis of mania but not \> 14 days before Screening. Hospital admission must be a result of the current manic episode.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (31)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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BurgasBulgariaUnknown status
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KazanlakBulgariaUnknown status
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PlovdivBulgariaUnknown status
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SlivenBulgariaUnknown status
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SofiaBulgariaUnknown status
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BrasovRomaniaUnknown status
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BucharestRomaniaUnknown status
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IașiRomaniaUnknown status
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BelgradeSerbiaUnknown status
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KovinSerbiaUnknown status
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KragujevacSerbiaUnknown status
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NišSerbiaUnknown status
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Novi KneževacSerbiaUnknown status
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AnaheimUnited StatesUnknown status
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AtlantaUnited StatesUnknown status
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BentonvilleUnited StatesUnknown status
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CerritosUnited StatesUnknown status
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ChicagoUnited StatesUnknown status
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CincinnatiUnited StatesUnknown status
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GaithersburgUnited StatesUnknown status
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Glen OaksUnited StatesUnknown status
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HialeahUnited StatesUnknown status
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Little RockUnited StatesUnknown status
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MiamiUnited StatesUnknown status
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Miami LakesUnited StatesUnknown status
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OrangeUnited StatesUnknown status
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RichardsonUnited StatesUnknown status
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StockbridgeUnited StatesUnknown status
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TampaUnited StatesUnknown status
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TorranceUnited StatesUnknown status
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West Palm BeachUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.