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Study identifier: NCT03078322 Synced from ClinicalTrials.gov · August 09, 2026
● Study status: CompletedELEVATE

AV-101 as Adjunct Antidepressant Therapy in Patients With Major Depression

Condition: Major Depressive Disorder  ·  Sponsor: VistaGen Therapeutics, Inc.

PhasePhase 2
Planned participants180
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where22 locations
For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.Open the site landscape →

About this study

The study will evaluate the safety and efficacy of AV-101.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Diagnosed with MDD, single or recurrent, and currently experiencing a MDE of at least 8 weeks in duration. * Has a history of inadequate response to at least 1 approved antidepressant including at least 1 and no more than 3 during the current depressive episode. * Meet the threshold on the total HAMD-17 score of \> 20 * If female, a status of nonchildbearing potential or use of an acceptable form of birth control. * Body mass index between 18 to 40 kg/m2. * Other criteria may apply Exclusion Criteria: * History of bipolar disorder, schizophrenia or schizoaffective disorders, or any history of psychotic symptoms in the current or previous depressive episodes. * Any Axis I or Axis II Disorder, which at screening is clinically predominant to their MDD or has been predominant to their MDD at any time within 6 months prior to screening. * Women who are pregnant or breastfeeding or a positive pregnancy test at screening or baseline. * Currently taking a prohibited adjunct therapy. Such drugs must be washed out for at least 4 weeks prior to baseline. * Current diagnosis of moderate or severe substance use (including alcohol) disorder (abuse or dependence, as defined by DSM-5), with the exception of nicotine dependence, at screening or within 6 months prior to screening. * In the opinion of the investigator, the subject has a significant risk for suicidal behavior * Has received electroconvulsive therapy, or had repetitive transcranial magnetic stimulation in the current episode. * Has received vagus nerve stimulation at any time prior to screening. * Any current or past history of any physical condition, which in the investigator's opinion might put the subject at risk or interfere with study results interpretation.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (22)

VistaGen Investigational SiteGarden Grove, California, United States
VistaGen Investigational SiteLos Angeles, California, United States
VistaGen Investigational SiteNational City, California, United States
VistaGen Investigational SiteOakland, California, United States
VistaGen Investigational SiteSan Diego, California, United States
VistaGen Investigational SiteTemecula, California, United States
VistaGen Investigational SiteFort Myers, Florida, United States
VistaGen Investigational SiteJacksonville, Florida, United States
VistaGen Investigational SiteAtlanta, Georgia, United States
VistaGen Investigational SiteAugusta, Georgia, United States
VistaGen Investigational SiteHoffman Estates, Illinois, United States
VistaGen Investigational SiteLake Charles, Louisiana, United States

+ 10 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

Garden GroveLos AngelesNational CityOakland

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