Multicenter Study to Assess the Efficacy and Safety of LB-102 in the Treatment of Adult Patients With BP1MDE.

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-65
SponsorLB Pharmaceuticals Inc.

About this trial

Phase II study for patients with Bipolar 1 Disorder experiencing major depressive episode. Patient eligible for enrollment will be randomized (like flipping a coin) to either active drug (LB-102 or placebo). Treatment is for 6 weeks.

Eligibility criteria

Qualifiers

Sign IRB approved ICF, Stable living environment

Diagnosis of Bipolar1 disorder defined by criteria in the DSM 5 and currently experiencing a MDE without psychotic or mixed features, and supported by the SCID 5 CT

Currently experiencing an MDE that began at least 4 weeks but no more than 18 months prior to randomization

Currently treated in an out-patient environment

Disqualifiers

Sexually active woman of childbearing potential and male who are not practicing 2 different methods of birth control or woman who is currently breast feeding

History of non-response to 2 adequate medication trials for depressive symptoms

Improvement of ≥20% in MADRS 10 total score between the screening and baseline assessments

Have bipolar disorder with mixed features or considered as rapid cyclers

Trial design

Treatments tested in this trial

  • LB-102
  • Placebo

Treatment groups

320 Participants
are divided into 2 treatment groups

Sponsors and collaborators