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Study identifier: NCT07363577 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Evaluate LB-102 for the Treatment of Adult Patients With Acute Schizophrenia

Condition: Schizophrenia  ·  Sponsor: LB Pharmaceuticals Inc.

PhasePhase 3
Planned participants456
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

This is a Phase 3, randomized, double blind, placebo controlled, fixed dose, study designed to evaluate the efficacy, safety, tolerability, and of LB-102 versus placebo for the treatment of adult patients with an acute exacerbation of schizophrenia.

This description comes directly from the study's public registry record.

Talk to the study team

Branislav Mancevski, MD  ·  212-605-0300  ·  clinicaltrials@lbpharma.us

Always discuss trial participation with your own doctor first.

Locations (13)

Pillar Clinical ResearchBentonville, Arkansas, United StatesRecruiting
Pillar Clinical ResearchLittle Rock, Arkansas, United StatesRecruiting
Woodland International Research GroupLittle Rock, Arkansas, United StatesRecruiting
ProScience Research GroupCulver City, California, United StatesRecruiting
CenExelGarden Grove, California, United StatesRecruiting
Synergy San DiegoLemon Grove, California, United StatesRecruiting
Clinical Innovations, Inc.Riverside, California, United StatesRecruiting
Health Synergy Clinical ResearchBoynton Beach, Florida, United StatesRecruiting
Innovative Clinical ResearchMiami Lakes, Florida, United StatesRecruiting
Accelerated Clinical TrialSnellville, Georgia, United StatesRecruiting
Pillar Clinical ResearchChicago, Illinois, United StatesRecruiting
Arch Clinical TrialsSt Louis, Missouri, United StatesRecruiting

+ 1 more locations — full list on the registry record.

Follow this study

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Source record: clinicaltrials.gov/study/NCT07363577