Phase 3 Depression and Anxiety Trial, Recruiting NCT07412756 Sponsor: Eli Lilly and Company Condition: Depression and Anxiety
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Phase 3 Depression and Anxiety Trial, Recruiting

NCT07412756
Recruiting Phase 3 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with major depressive disorder (a form of clinical depression) according to recognised diagnostic standards.
  • People who are already taking a stable, prescribed medication for major depressive disorder.
  • People who are willing and able to commit to the full duration of the study, attend all required visits, give themselves injections of the study medication, store the study medication correctly, keep electronic and paper diaries as required, and complete questionnaires throughout the study.

Who may not be able to join:

  • People who have ever been diagnosed with, or currently have, schizophrenia or another psychotic disorder, bipolar disorder, borderline personality disorder, or any eating disorder.
  • People who have type 1 diabetes, or a history of a dangerous build-up of acids in the blood (ketoacidosis), or a history of a serious diabetes-related condition involving very high blood sugar levels or loss of consciousness.
  • People who have had a moderate or severe problem with substance or alcohol use within the 180 days before the screening appointment.
  • People who are currently at risk of suicide or are considered by the study team to be at significant risk of suicide.
  • People who have taken part in another clinical study and received an active treatment (or where it is unknown whether they received an active treatment) within 90 days or 5 half-lives of the study drug — whichever period is longer — before screening (confirm with trial site).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST), Eli Lilly and Company

Phone: 1-317-615-4559

Australian sites

NeuroCentrix, Carlton,
61395460009
Lyell McEwin Hospital, Elizabeth Vale,
0881829554
Barwon Health, Geelong,
Multidisciplinary Alfred Psychiatry Research Centre, Melbourne,
Paratus Clinical Research - Melbourne, Melbourne,
Toowoomba Hospital, Toowoomba,
Westmead Hospital, Westmead,

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
9 February 2026
Est. completion
1 February 2028

Where this trial is recruiting

🇦🇺 Australia 🇧🇷 Brazil 🇨🇦 Canada 🇨🇳 China 🇩🇪 Germany 🇬🇷 Greece 🇯🇵 Japan 🇲🇽 Mexico 🇵🇱 Poland Puerto Rico 🇰🇷 South Korea 🇪🇸 Spain 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

7 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Time to Relapse Defined as the Number of Days from Randomization to Date on Which the Participant Meets Any Relapse Criterion of Major Depressive Disorder (MDD)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov