Phase 2
Completed N=23
Examining the Impact of Sirolimus on Ketamine's Antidepressant Effects
Source: ClinicalTrials.gov NCT02487485 ↗Enrolled (actual)
23
Serious AEs
0.0%
Results posted
Jul 2020
Primary outcomePrimary: Montgomery-Asberg Depression Rating Scale — 27.9387; 26.5756; 16.5482; 20.9065 score on a scale
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Montgomery-Asberg Depression Rating Scale |
27.9387; 26.5756; 16.5482; 20.9065 | — |
| SECONDARY Quick Inventory of Depressive Symptoms (QIDS) |
12.6342; 11.3942; 9.1193; 10.6699 | — |
| SECONDARY Hamilton Anxiety Rating Scale (HAMA) |
12.9678; 13.8222; 9.8755; 10.8669 | — |
| SECONDARY Clinician Administered Dissociative States Scale (CADSS) |
12.1; 13.95 | — |
| SECONDARY Positive and Negative Symptom Scale (PANSS) - Positive |
9.1537; 8.9444 | — |
| SECONDARY Rapamycin Level |
26.5; 0 | — |
| SECONDARY Ketamine Level |
115; 125 | — |
Eligibility Criteria
Inclusion Criteria
- Veterans and non-Veterans between the ages of 21-65.
- Diagnosis of Major Depressive Episode (unipolar or bipolar) as determined by the Mini International Neuropsychiatric Interview (MINI).
- Antidepressant-resistant depressive symptoms, defined by a history of failure of one or more adequate antidepressant trials.
- 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.
- Stable course of psychotherapy (if engaged in) for a period of four weeks or longer at the time of randomization.
- 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.
- Able to provide written informed consent according to VA HSS guidelines.
- Ability to read and write in English.
- A score greater than or equal to 18 on the Montgomery Åsberg Depression Rating Scale (MADRS).
Exclusion Criteria
- 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.
- Current, ongoing serious suicidal risk as assessed by evaluating investigator or by scoring 5 or more on the item-10 of the MADRS.
- Patients with unstable or inadequately controlled medical conditions.
- Patient requiring prohibited medication.
- Patient with history of organ transplant.
- Meet criteria for a diagnosis of substance dependence (amphetamines, cocaine, hallucinogens, inhalants, opioids, sedatives/hypnotics/anxiolytics) within the three months prior to screening date.
- Positive urine drug screen for cannabis, cocaine, PCP, or barbiturates.
- Positive pregnancy test at screening at any screen given during the study.
- Known sensitivity to sirolimus or ketamine.
- History of sensitivity to heparin or heparin-induced thrombocytopenia.
- 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.
Data sourced from ClinicalTrials.gov (NCT02487485). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.