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A Study of Brenipatide in Adult Participants With Major Depressive Disorder

RecruitingPhase 3

Sponsor: Eli Lilly and Company

Conditions: Depressive Disorder, Major

Interventions: Brenipatide, Placebo

Countries: United States, Australia, Brazil, Canada, China, Germany, Greece, Japan

This study evaluates the safety and efficacy of brenipatide when administered with standard of care (SoC) compared to placebo plus SoC in delaying the return of major depressive symptoms. The trial is divided into three periods as follows: a screening period that will last approximately 1 month, a treatment period that will last a minimum of 12 months, and the follow up period that will last approximately 2 months. The duration of study participation may vary and may be shortened if depression symptoms worsen or if withdrawal from the study occurs for any reason.

Eligibility overview

Sex: ALL

Age: 18 Years to 75 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* Meet the diagnostic criteria for major depressive disorder
* Are on a stable standard of care medication for major depressive disorder
* Are reliable and willing to make themselves available for the duration of the study and attend required study visits, and are willing and able to follow study procedures as required, such as

  * self-inject study intervention
  * store and use the provided blinded study intervention, as directed
  * maintain electronic and paper study diaries, as applicable, and
  * complete the required questionnaires

Exclusion Criteria:

* Have a lifetime history or current diagnosis of the following:

  * schizophrenia or other psychotic disorder
  * bipolar disorder
  * borderline personality disorder, or
  * any eating disorder.
* Have type 1 diabetes mellitus, or a history of

  * ketoacidosis, or
  * hyperosmolar state or coma.
* Evidence of moderate or severe substance or alcohol use disorder within 180 days of screening
* Are actively suicidal or deemed a significant risk for suicide
* Have participated in a clinical study and received active treatment, or unknown if they received active treatment, within 90 days or 5 half-lives (whichever is longer) before screening

Locations (180)

Moorpark, California, United States
Orange, California, United States
New Haven, Connecticut, United States
Hollywood, Florida, United States
Maitland, Florida, United States
Miami Gardens, Florida, United States
Miami Lakes, Florida, United States
Naples, Florida, United States
Orange City, Florida, United States
Orlando, Florida, United States
Tampa, Florida, United States
Decatur, Georgia, United States
Indianapolis, Indiana, United States
Waterloo, Iowa, United States
Baltimore, Maryland, United States
Boston, Massachusetts, United States
Foxborough, Massachusetts, United States
Watertown, Massachusetts, United States
Troy, Michigan, United States
St Louis, Missouri, United States
Las Vegas, Nevada, United States
New York, New York, United States
Portland, Oregon, United States
Media, Pennsylvania, United States
Philadelphia, Pennsylvania, United States
Sioux Falls, South Dakota, United States
DeSoto, Texas, United States
Fort Worth, Texas, United States
Shavano Park, Texas, United States
Clinton, Utah, United States
+ 150 more on CT.gov