Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Placebo + ADT refers to a control treatment arm used in clinical trials, specifically those conducted by Otsuka Pharmaceutical for Major Depressive Disorder (MDD). In this regimen, patients receive an inactive placebo alongside an open-label, marketed antidepressant therapy (ADT) to which they previously showed an incomplete response. The ADT typically consists of standard-of-care agents such as selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitors (SNRIs). This combination serves as a comparator to evaluate the efficacy and safety of adjunctive treatments, such as aripiprazole or brexpiprazole, when added to existing antidepressant therapy. The placebo component contains no active pharmacological ingredient, while the ADT component provides the baseline therapeutic effect against which the investigational drug's adjunctive benefit is measured.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on placebo + ADT.