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CompletedPhase 2Results posted

Examining the Impact of Sirolimus on Ketamine's Antidepressant Effects

NCT02487485 · Yale University

Closed to entry
Status
Not accepting participants
Phase 2
Phase
23
Target enrolment
2
Study sites
1 US states

What it is testing

Summary

The aim of the study is to provide insight into the impact of the immunosuppressant drug sirolimus, on the antidepressant effects of the prototypal rapid-acting antidepressant medication, ketamine.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Montgomery-Asberg Depression Rating Scale

    Measured over Pretreatment and 2 week

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

21 Years to 65 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: 1. Veterans and non-Veterans between the ages of 21-65. 2. Diagnosis of Major Depressive Episode (unipolar or bipolar) as determined by the Mini International Neuropsychiatric Interview (MINI). 3. Antidepressant-resistant depressive symptoms, defined by a history of failure of one or more adequate antidepressant trials. 4. Stable doses of antidepressants (if prescribed) for a period of four weeks or longer at the time of randomization, except for MAOIs which are prohibited. 5. Stable course of psychotherapy (if engaged in) for a period of four weeks or longer at the time of randomization. 6. Females will be included if they are not pregnant or breastfeeding and agree to utilize a medically accepted birth control method (to include oral, injectable, or implant birth control, condom, diaphragm with spermicide, intrauterine device, tubal ligation, abstinence, or partner with vasectomy) or if post-menopausal for at least 1 year, or surgically sterile. For those women who are taking an oral contraceptive, we will also ask that they use (or ask their partners to use) a barrier method contraceptive. 7. Able to provide written informed consent according to VA HSS guidelines. 8. Ability to read and write in English. 9. A score greater than or equal to 18 on the Montgomery Åsberg Depression Rating Scale (MADRS). Exclusion Criteria: 1. Subjects with a diagnostic history of schizophrenia or schizoaffective disorder, or currently exhibiting manic or mixed episodes or psychotic features as confirmed by the Mini International Neuropsychiatric Inventory. 2. Current, ongoing serious suicidal risk as assessed by evaluating investigator or by scoring 5 or more on the item-10 of the MADRS. 3. Patients with unstable or inadequately controlled medical conditions. 4. Patient requiring prohibited medication. 5. Patient with history of organ transplant. 6. Meet criteria for a diagnosis of substance dependence (amphetamines, cocaine, hallucinogens, inhalants, opioids, sedatives/hypnotics/anxiolytics) within the three months prior to screening date. 7. Positive urine drug screen for cannabis, cocaine, PCP, or barbiturates. 8. Positive pregnancy test at screening at any screen given during the study. 9. Known sensitivity to sirolimus or ketamine. 10. History of sensitivity to heparin or heparin-induced thrombocytopenia. 11. Resting blood pressure lower than 85/55 or higher than 150/95, or resting heart rate lower than 45/min or higher than 100/min.

Where

2 study sites

FacilityCityRegionCountry
Yale New Haven HospitalNew HavenConnecticutUnited States
West Haven Veterans AffairsWest HavenConnecticutUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT02487485 on ClinicalTrials.gov →

Last updated in the registry 2020-07-16. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits