Study to Assess the Adverse Events of Oral ABBV-932 in Adult Participants With Depressive Episodes Associated With Bipolar I or II Disorder

Recruiting now · Phase 2

Conditions studied: Bipolar I or II Disorder

In brief

Bipolar disorder is a severe chronic mood disorder that affects up to 4% of the adult population in the United States. The purpose of this study is to assess how safe and effective ABBV-932 is in treating participants with depressive episodes associated with bipolar I or II disorder. ABBV-932 is an investigational drug being developed for the treatment of depressive episodes in adult participants with bipolar I or II disorder. Participants with bipolar I or II disorder who are currently experiencing a depressive episode will enter the study and be treated with open-label ABBV-932. Approximately 200 adult participants with bipolar I or II disorder will be enrolled in approximately 50 sites in the United States and Puerto Rico. Participants will receive oral capsules of ABBV-932 for a 26-week treatment period. The treatment period will be followed by a safety follow-up (SFU) period of 30 days. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regularly scheduled visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.

Key facts

Study ID: NCT07220460
Run by: AbbVie
People needed: 200
Starts: 2025-09-30
Expected to finish: 2027-04-01
Last updated by the study team: 2026-06-18

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Body Mass Index (BMI) >= 18.0 to <= 40.0 kg/m\^2, inclusive.
Participants who currently meet the Diagnostic and Statistical Manual of Mental Disorders treatment (DSM-5-TR) criteria for bipolar I or II disorder without psychotic features based on the Mini International Neuropsychiatric Interview (MINI 7.0.2), currently experiencing a depressive episode of at least 4 weeks and not exceeding 12 months.
Normal physical examination findings, clinical laboratory test results, vital signs, and 12-lead ECG results at screening or abnormal results that are judged not clinically significant by the investigator and documented as such in the eCRF
Participant with the following psychiatric history:
No history of psychiatric hospitalization (inpatient or intensive outpatient) in the past 3 months prior to screening.
No lifetime history of schizophrenia, other psychotic disorders, dissociative disorders, or neurocognitive disorders.
No history of moderate or severe substance use disorder (except nicotine) in the past 6 months prior to screening.
History of stable psychiatric comorbidities (e.g., PTSD, OCD) may be included provided these conditions have not required intervention with a prohibited medication within the past 12 months prior to Screening.

You may not qualify if…

A total score greater than 12 on the Young Mania Rating Scale (YMRS) at baseline.
History of an allergic reaction or significant sensitivity to constituents of the study drug (and its excipients) and/or other products in the same class.
A concurrent medical condition that might interfere with the conduct of the study, confound the interpretation of the study results, or endanger the subject's well-being. This includes any unstable condition, history or evidence of malignancy (other than treated basal or squamous cell carcinoma), or any significant hematologic, endocrine, cardiovascular, respiratory, renal impairment or disease (e.g., participants with eGFR < 30 mL/min), hepatic (including history of severe hepatic impairment), gastrointestinal, or neurological disorder. If there is a history of such disease (except malignancy), but the condition has been stable for more than 1 year, does not require treatment with prohibited medications, and is judged by the investigator not to interfere with participation in the study, the subject may be included.

Where it is running

BDH Research /ID# 274677 — San Juan, Puerto Rico (enrolling)
Advanced Research Center /ID# 273474 — Anaheim, California, United States (enrolling)
Axiom Research /ID# 273482 — Colton, California, United States (enrolling)
Collaborative Neuroscience Research - Garden Grove /ID# 273492 — Garden Grove, California, United States (enrolling)
Sun Valley Research Center /ID# 273472 — Imperial, California, United States (enrolling)
Synergy San Diego /ID# 278340 — Lemon Grove, California, United States (enrolling)
Alliance for Research Alliance for Wellness /ID# 273477 — Long Beach, California, United States (enrolling)
Nrc Research Institute - Los Angeles /ID# 278450 — Los Angeles, California, United States (enrolling)
Excell Research /ID# 273483 — Oceanside, California, United States (enrolling)
Inland Psychiatric Medical Group /ID# 273471 — Temecula, California, United States (enrolling)
Sunwise Clinical Research /ID# 278165 — Walnut Creek, California, United States (enrolling)
Connecticut Clinical Research - Cromwell /ID# 278116 — Cromwell, Connecticut, United States (enrolling)
Clinical Neuroscience Solutions Healthcare - Jacksonville /ID# 278332 — Jacksonville, Florida, United States (enrolling)
GMI Florida - Central Miami Medical Institute /ID# 273486 — Miami, Florida, United States (enrolling)
Allied Biomedical Res Inst Inc /ID# 273476 — Miami, Florida, United States (enrolling)
Floridian Clinical Research - Miami Lakes /ID# 279379 — Miami Lakes, Florida, United States (enrolling)
K2 Medical Research - Orlando - South Orlando Avenue /ID# 273487 — Orlando, Florida, United States (enrolling)
Apg Research /ID# 278439 — Orlando, Florida, United States (enrolling)
Segal Trials - West Broward Outpatient Research Site /ID# 273496 — Tamarac, Florida, United States (enrolling)
Health Synergy Clinical Research /ID# 279384 — West Palm Beach, Florida, United States (enrolling)
Trialmed /ID# 278046 — Atlanta, Georgia, United States (enrolling)
Atlanta Center for Medical Research /ID# 278827 — Atlanta, Georgia, United States (enrolling)
Revive Research Institute - Elgin /ID# 279756 — Elgin, Illinois, United States (enrolling)
Ima Clinical Research Phoenix (Alea) /ID# 278047 — Phoenix, Arizona, United States (enrolling)
Pharmasite Research, Inc. /ID# 279163 — Baltimore, Maryland, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.