Early Phase 1 Depression and Anxiety Trial, Recruiting NCT07560878 Sponsor: Mclean Hospital Condition: Depression and Anxiety
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Early Phase 1 Depression and Anxiety Trial, Recruiting

NCT07560878
Recruiting Early Phase 1

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 are medically able to safely receive TMS (a type of brain stimulation) and the study medications.
  • People whose medication routine has been stable for at least one month before the study and who are able to keep it stable throughout the study.
  • People who are not currently receiving TMS, ECT (electroconvulsive therapy), or ketamine treatment.
  • People who do not have active safety concerns related to suicidal thoughts or behaviours.
  • People with moderate to severe Major Depressive Disorder, as measured by a standard depression questionnaire.

Who may not be able to join:

  • People with a history of seizures or epilepsy.
  • People with a history of any condition, injury, or abnormality affecting the inside of the skull or brain.
  • People with a history of traumatic brain injury that involved loss of consciousness lasting more than 15 minutes.
  • People who show signs of increased pressure inside the skull.
  • People with a significant neurological condition, such as a recent stroke, brain tumour, or a degenerative brain disease (confirm with trial site for full list).
  • People with serious medical conditions that could become dangerous if a seizure were to occur, such as certain heart or breathing conditions (confirm with trial site for full list).
  • People with severe migraines that may make it difficult to tolerate the treatment.
  • People who are unable to tolerate an MRI scan.
  • People who are pregnant.
  • People with a known allergic reaction to any of the following study drugs: d-cycloserine, baclofen, memantine, or lorazepam.

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 21 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Principal Investigator: Joshua C Brown, MD, PhD, Mclean Hospital

Phone: 617-855-2153

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
Early Phase 1
Sponsor
Mclean Hospital
Registry
ClinicalTrials.gov
Start date
11 March 2026
Est. completion
1 December 2030

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in P30 TEP Peak Amplitude; Change in N45 TEP Peak Amplitude; Change in N100 TEP Peak Amplitude

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: 21 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