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Phase 2 Completed N=23 Randomized Triple-blind Other

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

OutcomeResultp-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.
View full record on ClinicalTrials.gov →

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.

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