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

NCT07363577 · NOVA2 Phase 3Recruiting

Lead sponsor
LB Pharmaceuticals Inc. (Industry)
Enrollment
456 (estimated)
Start date
25 Mar 2026
Primary completion
Jun 2027 (estimated)
Study completion
1 Oct 2027
Last update posted
27 Jul 2026

Design

Study type
Interventional
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential
Masking
Quadruple
Arms
3

Interventions

  • LB-102 (50 mg tablet) Drug
  • LB-102 (100 mg tablet) Drug
  • Placebo Other

Conditions and primary outcome

  • Schizophrenia

Primary outcome

Change from baseline to Week 6 on the Positive and Negative Syndrome Scale (6 weeks)

Posted results on ClinicalTrials.gov

Results posted on ClinicalTrials.gov: No

Results from company and journal sources

No editor-confirmed results are on record for this study.

Publications

No PubMed citation lists NCT07363577.

CT-VCA trial quality

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Data integrity

Compare what the registry, company releases, FDA documents and publications say about this study.

Drugs on HealthTrade

Source

Source: ClinicalTrials.gov, U.S. National Library of Medicine. Listing a study does not mean NLM has evaluated it.

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