Overview

Maintenance Ketamine Infusions for Treatment-Resistant Bipolar Depression

Status:
Not yet recruiting
Trial end date:
2024-08-31
Target enrollment:
0
Participant gender:
All
Summary
Growing evidence has supported rapid and robust antidepressant effects with subanesthetic doses of intravenous (IV) ketamine for treatment resistant depression (TRD). However, no completed or ongoing RCTs have evaluated the effects of repeated doses of IV ketamine for a homogenous sample of patients with treatment-resistant bipolar disorder depression (TRBD). The primary research goal is to determine the acute antidepressant efficacy, safety and tolerability of repeated sub-anesthetic maintenance doses of IV ketamine in, over a period of twelve weeks. Open-label ketamine infusions will be provided on a flexible schedule (every 2-4 weeks) with flexible dosing (0.5-1.0mg/kg over 40 minutes) titrated to optimize benefits, while minimizing the dosage and frequency over a 12-week extension period. All patients participating in this open-label study will have completed an acute course of infusions in a parent two-site, phase II, double-blinded midazolam-controlled RCT trial. In addition to this acute course of four infusions, a maximum of six infusions will be provided over the 12-week period. Secondary aims include evaluating effects of IV ketamine on suicidal ideations, quality of life, function and duration of effects. Herein, a two-site (University Health Network and Canadian Rapid Treatment Centre of Excellence), single-arm, open label, 12-week extension trial evaluating the effects of flexibly-dosed adjunctive ketamine infusions for TRBD to maintain antidepressant effects in participants who achieved an antidepressant response (MADRS decrease by >50%) or remission (MADRS < 12) following an acute course of four ketamine infusions is proposed. The primary outcome will be Montgomery-Åsberg Depression Rating Scale (MADRS) scores, determining by a linear mixed model from baseline to week 12. Secondary outcomes include evaluating response and remission rates, safety, tolerability (including treatment-emergent mania), and effects on suicidality, anxiety, quality of life, function and the duration of effects.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Health Network, Toronto
Collaborator:
Dr. Joshua Rosenblat
Treatments:
Ketamine
Criteria
Inclusion Criteria:

1. Provide written, voluntary informed consent prior to study enrollment. Substitute
decision makers will not be allowed to consent to study on a potential patient's
behalf.

2. Male or female between the age of 21 to 65, inclusive.

3. Meets DSM-5 criteria for Bipolar I or II Disorder, currently experiencing a Major
Depressive Episode without psychotic features. Diagnosis confirmed by study
psychiatrist at the start of the parent KET-BD randomized clinical trial (RCT).

4. Participant in the KET-BD RCT 4a. Participants in the ketamine arm of the KET-BD RCT
must have experienced an antidepressant response (i.e. change in MADRS score ≥ 50% at
day 14 compared to baseline or Clinical Global Impression-Improvement (CGI-I) = 2
'much improved' or 1 'very much improved') or experienced clinical remission of
symptoms (i.e., MADRS score < 12 on day 14) 4b. Participants in the midazolam arm of
the KET-BD RCT must present as moderately to severely depressed (MADRS >21) on days 14
and 28 of the parent RCT and must be responders or remitters following four flexibly
dosed infusions over 2 weeks.

5. Current depressive episode has inadequate response to two or more adequate first-line
treatment trials for bipolar depression, as per the 2018 CANMAT Bipolar Disorder
Guidelines. First line treatment trials include the use of lithium, valproate,
carbamazepine, lamotrigine and/or any antipsychotic medication. Adequate medications
confirmed at the start of the parent KET-BD RCT.

6. Patient must be receiving guideline-concordant pharmacotherapy without changes in the
last month, including a therapeutic dose of a mood stabilizer.

Exclusion Criteria:

1. Currently exhibiting symptoms of mania, hypomania, or mixed state bipolar, as
determined by the Young Mania Rating Scale (YMRS) score greater than 12.

2. Current symptoms of psychosis or a substance use disorder within the past 3 months.
History of psychotic features during a mood episode will not be excluded.

3. History of neurological disorders (including, but not limited to, uncontrolled seizure
disorder, history of stroke within past 12 months, major head injuries, aneurysmal
vascular disease [including thoracic and abdominal aorta, intracranial, and peripheral
arterial vessels], arteriovenous malformation, or intracerebral hemorrhage)

4. Lifetime history of a primary psychotic disorder (including, but not limited to,
schizophrenia or schizoaffective disorder)

5. Lifetime history of ketamine use disorder

6. Presence of active suicidality, requiring involuntary inpatient treatment or recent
suicide attempts within the past 3 months.

7. Presence of a contraindication to ketamine, including a drug allergy, uncontrolled
hypertension (baseline systolic blood pressure > 140 mmHg and/or diastolic blood
pressure > 90 mmHg), low or labile blood pressure, myocardial infarction within past
12 months, cardiac arrhythmia, moderate to severe hepatic impairment (i.e., Child-Pugh
score of B or C), moderate or severe renal impairment (glomerular filtration rate
(GFR) < 45 milliliters/min), heart failure, or coronary artery disease

8. Pregnant or breastfeeding women or women who intend to get pregnant. Patients who are
sexually active must agree to use a highly effective contraceptive method (as outlined
in section 5.9).

9. Use of prohibited concomitant medications, including other forms of ketamine or
esketamine, benzodiazepines, monoamine oxidase inhibitors, stimulants, medical or
recreational cannabis of any form.

10. Patients in the ketamine-arm of the parent RCT, that did not reasonably tolerate 4
infusions of flexibly-dosed ketamine, as determined by the investigator and/or patient