Condition: Schizophrenia · Sponsor: LB Pharmaceuticals Inc.
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.
Branislav Mancevski, MD · 212-605-0300 · clinicaltrials@lbpharma.us
Always discuss trial participation with your own doctor first.
| Pillar Clinical Research | Bentonville, Arkansas, United States | Recruiting |
| Pillar Clinical Research | Little Rock, Arkansas, United States | Recruiting |
| Woodland International Research Group | Little Rock, Arkansas, United States | Recruiting |
| ProScience Research Group | Culver City, California, United States | Recruiting |
| CenExel | Garden Grove, California, United States | Recruiting |
| Synergy San Diego | Lemon Grove, California, United States | Recruiting |
| Clinical Innovations, Inc. | Riverside, California, United States | Recruiting |
| Health Synergy Clinical Research | Boynton Beach, Florida, United States | Recruiting |
| Innovative Clinical Research | Miami Lakes, Florida, United States | Recruiting |
| Accelerated Clinical Trial | Snellville, Georgia, United States | Recruiting |
| Pillar Clinical Research | Chicago, Illinois, United States | Recruiting |
| Arch Clinical Trials | St Louis, Missouri, United States | Recruiting |
+ 1 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07363577