(Le sommaire est en français; le reste du document est en anglais.)
- Le trouble dépressif majeur (TDM) est un trouble commun de santé mentale récurrent et débilitant. Environ 10 % à 30 % des patients atteints de TDM n’atteindront pas la rémission clinique complète malgré l’utilisation de plusieurs traitements pharmacologiques aux antidépresseurs — cette sous-population de patients est considérée comme ayant une dépression résistante aux traitements (DRT). La DRT est un trouble dépressif difficile à traiter et les traitements disponibles sont souvent limités en raison d’effets secondaires psychologiques et physiologiques importants.
- L’eskétamine est l’énantiomère S de la kétamine racémique et on élabore actuellement un vaporisateur nasal pour usage thérapeutique potentiel chez les patients atteints de DRT. Aucun pays n’a encore approuvé ce dispositif, mais il fait l’objet d’une évaluation prioritaire à Santé Canada et a récemment reçu l’approbation de la FDA.
- Dans un essai de phase III, l’eskétamine associée à un antidépresseur nouvellement lancé a démontré une amélioration statistiquement significative des scores de l’échelle Montgomery-Åsberg Depression Rating Scale (MADRS) par rapport à un placébo et un antidépresseur nouvellement lancé. L’eskétamine associée à un antidépresseur oral nouvellement lancé a aussi réduit significativement le nombre de rechutes ou retardé la survenance d’une rechute.
- Comme pour la kétamine, des effets dissociatifs, de sédation et d’élévations de la tension artérielle ont été signalés. La plupart de ces effets secondaires sont légers ou modérés et résolus quelques heures suivant l’administration de l’eskétamine.
- Les propriétés psychoactives de l’eskétamine lui confèrent un potentiel de dépendance et d’abus; des politiques visant à limiter son utilisation hors indication et des lignes directrices sur sa distribution seraient importantes pour prévenir son détournement. En outre, il subsiste un manque de preuves comparant l’eskétamine en vaporisation nasale à d’autres stratégies d’appoint courantes pour la DRT.
These bulletins are not systematic reviews and do not involve critical appraisal or include a detailed summary of study findings. Rather, they present an overview of the technology and available evidence. They are not intended to provide recommendations for or against a particular technology.
Literature Search Strategy
A limited literature search was conducted using the following bibliographic databases: MEDLINE, Embase, PsychInfo, PubMed, and the Cochrane Library. Grey literature was identified by searching relevant sections of the Grey Matters checklist (https://www.cadth.ca/grey-matters). No methodological filters were applied. The search was limited to English-language documents but not limited by publication year. Regular alerts updated the search until project completion; only citations retrieved before March 13, 2019 were incorporated into the analysis.
One author screened the literature search results and reviewed the full text of all potentially relevant studies. Studies were considered for inclusion if the intervention was esketamine (S-ketamine) and studied for treatment-resistant depression in a phase III trial. Conference abstracts and grey literature were included when they provided additional information to that available in the published studies.
A draft version of this bulletin was reviewed by one clinical expert. The drug manufacturer also provided input on an earlier draft of this report.
Major depressive disorder (MDD) is a common, debilitating, and recurrent mental health disorder. MDD is characterized by symptoms of persistent low mood, changes in appetite and sleep, fatigue, loss of motivation, interest or pleasure, or feelings of worthlessness.1 It can also be associated with a substantial loss in productivity, quality of life, and increased mortality from suicide. MDD has a significant global burden, with an estimated 300 million people affected and reported as the leading cause of disability of all of the mental illnesses worldwide.2-4 Within Canada, approximately 11% (4.1 million) of the population have reported a major depressive episode in their lifetime.1,5 Even with available therapies, a significant proportion of patients will not reach complete clinical remission, with approximately 10% to 30% not responding to multiple antidepressants.6,7
Treatment-resistant depression (TRD) is the clinical term used to define this subpopulation of MDD patients that have not achieved optimal response to conventional therapy. TRD presents an even greater burden, with an increased risk for subsequent relapses and suicide.8,9 Patients with TRD are also twice as likely to be hospitalized, incurring additional medical costs.8,10 Risk factors for TRD may include old age, high stress levels, concomitant psychiatric disorders, and a history of medication nonadherence.6
The most common definition of TRD is the inadequate response to two or more antidepressants.7,10,11 However, there is no clear consensus surrounding this definition, with only 17% of treatment studies closely matching this definition.10 Variations in this definition can be attributed to inconsistencies in the use of adjunctive therapies, variable dose and duration of an adequate treatment trial, and whether treatment failure occurred in the current depressive episode. As studies of emerging treatments utilize diverse definitions of TRD, it can be difficult to translate research findings into practical guidelines.
TRD is a more challenging depressive disorder to treat, with few strong recommendations in clinical practice guidelines. None of the available options have demonstrated superiority in improving clinical outcomes for patients with TRD.7 Available therapies are also often limited by significant side effects, such as weight gain and sedation. There remains an unmet need for a safe and effective treatment of TRD for which esketamine offers the potential to address.
Janssen Research & Development is currently investigating esketamine for its potential therapeutic use in patients with MDD who are refractory to classical antidepressants.7 Esketamine is the S-enantiomer of racemic ketamine — a drug that has been used traditionally as a general anesthetic. In studies, sub-anesthetic intravenous doses of ketamine have demonstrated rapid antidepressant effects, as well as lessened fatigue and suicidality in patients with TRD and with minimal negative impacts on cognitive functioning.12,13 Due in part to these promising results and despite concerns around limited data on long-term safety and duration of effect, ketamine’s use for depression has expanded from research settings to specialized clinics in the US and Canada servicing this patient population.14,15
Esketamine is approximately three to four times more potent than R-ketamine, potentially translating into lower doses with fewer side effects compared with previously studied ketamine infusions.7,16,17 Esketamine’s antidepressant effects are not mediated by known mood-modulating pathways such as the monoamine, gamma-aminobutyric acid (GABA), or opioid axes. Although the specific mechanism of action has not been fully elucidated, it is postulated that esketamine acts primarily to block the N-methyl-D-aspartate (NMDA) receptor and activate the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor.
For TRD (defined by the manufacturer as MDD that has not responded adequately to at least two different antidepressants of adequate dose and duration in the current depressive episode), esketamine is formulated as a single-use nasal spray device.18 In contrast to intravenous ketamine, which is limited to outpatient clinics, intranasal administration is easier and could allow for increased access to therapy.19 Each device contains 28 mg of drug, delivered as one spray in each nostril.18 The maximum dose studied in clinical trials was 84 mg; therefore, multiple devices may be required. Priming of the device is not required but a five-minute rest period in-between each device is advised. For acute treatment, esketamine nasal spray requires administration twice weekly for four weeks during treatment induction, then weekly for another four weeks, followed by weekly or every other week during ongoing maintenance.18 According to the manufacturer, it is intended to be used under the direct supervision of a health care professional.
As of the publication of this report, esketamine is approved in the US for TRD; it is not approved for use in other countries or for any other indication. The manufacturer has filed for regulatory approval in Canada and the European Union for adults with TRD (defined as MDD patients who have not responded adequately to at least two different antidepressants of adequate dose and duration in the current depressive episode) based on five, phase III clinical trials (Janssen Inc., Toronto, ON: personal communication, 2019 Feb 1).20-25 Health Canada is currently reviewing esketamine as a priority submission.26
In the US, the FDA has recently approved the marketing of esketamine nasal spray under the trade name Spravato, in conjunction with an oral antidepressant, “for the treatment of depression in adults who have tried other antidepressant medicines but have not benefited from them (treatment-resistant depression)”.27 It also received Breakthrough Therapy designation in 2016 from the FDA for MDD with imminent risk for suicide; this indication is not currently approved. Of note, the FDA grants a Breakthrough Therapy designation for drugs intended to treat a serious or life-threatening disease and where initial clinical data suggests that the drug may demonstrate substantial improvement over current therapies.28
Cost and Administration
The Canadian cost of esketamine is unavailable, as this product is not marketed in the country. For the US market, the manufacturer has announced that SPRAVATO will be priced at $590 for a 56 mg dose and $885 for 84 mg.29
Esketamine is developed to be administered as a nasal spray. The dosage regimen used in the completed and ongoing phase III trials is esketamine 28 mg, 56 mg, or 84 mg intranasally twice weekly for four weeks, followed by once weekly for four weeks, then once weekly or once every other week for ongoing maintenance therapy.18,20-24,30,31 As a result, the cost of therapy will vary based on the dose used per session and the number of treatment sessions administered, both of which can differ from patient to patient.
The budget impact is unknown, as the Canadian acquisition cost is not yet available.The budget impact will largely depend on its sequential place in therapy within the context of other treatment options currently on the market for MDD.
For the majority of patients with MDD, available medications, psychotherapy, and alternative therapies (e.g., electroconvulsive therapy, transmagnetic stimulation) are effective at relieving symptoms and achieving disease remission. However, MDD is a complex, heterogeneous disorder, and 10% to 30% of MDD patients do not respond to a sequence of multiple traditional antidepressant therapies.6,7
This subpopulation of patients with TRD could benefit from esketamine. However, the exact clinical need within this patient population is challenging to discern because of inconsistencies in the definitions of TRD, the variety of therapies currently available for TRD, the access to and reimbursement of non-pharmacological options, and the concurrent development of novel therapy options.
Because of limited evidence comparing available therapies, there is no standard treatment approach for TRD; therefore therapy should be individualized for each patient.6,7 The Canadian Network for Mood and Anxiety Treatments (CANMAT) guideline recommends making adjustments to therapy if there is no improvement within two to four weeks of initiating the antidepressant.11 The following options are recommended for managing an inadequate response:
- optimize the initial treatment
- switch the antidepressant class of drug
- add an adjunctive medication
- consider non-drug therapies.
Optimizing treatment involves increasing the dose of the current antidepressant, as tolerated, and continuing treatment for an additional six to eight weeks.11 Switching to an antidepressant of a different class is an alternative for patients who had no response to therapy, or who were not tolerating the initial antidepressant. CANMAT advises this strategy may be best employed for patients in their first antidepressant trial and therefore may not be the optimal strategy for TRD (i.e., failed two or more antidepressants).
An adjunctive strategy involves adding a second medication to the initial antidepressant. This strategy includes both augmentation (i.e., adding a non-antidepressant medication) and combination (i.e., adding an antidepressant from a different class).11 There is low-quality evidence to suggest that adjunctive therapy is more effective than switching therapy in patients who had a partial response to the initial antidepressant and have residual symptoms.7,11,32 Adjunctive medications that are recommended to try first are the following atypical antipsychotic drugs: aripiprazole, quetiapine, and risperidone (off-label).11,33 If a patient fails to respond despite these first-line options, they can trial the following adjunctive treatments: bupropion, mirtazapine, brexpiprazole, olanzapine, lithium, and thyroid hormone.11 Lastly, non-drug approaches to be considered for patients with TRD include psychotherapy and neurostimulation (e.g., transcranial magnetic stimulation, electroconvulsive therapy).
Summary of the Evidence
A total of five phase III trials evaluated the efficacy and safety of esketamine nasal spray in combination with a newly initiated oral antidepressant for patients with TRD; four were randomized, double-blind, active-controlled trials21-24 and one was an open-label safety study.20 There are an additional two phase III trials currently ongoing to further assess the efficacy and long-term safety of esketamine in this patient population.30,31 Details of these trials are summarized in Table 1.
In the active-controlled studies, patients were randomized to receive either esketamine nasal spray plus a newly initiated oral antidepressant or placebo nasal spray plus a newly initiated oral antidepressant. All previous oral antidepressants to which patients did not respond were discontinued.
In all of the phase III trials, TRD was defined as nonresponse (i.e., 25% or less improvement) to two or more oral antidepressants in the current episode of depression, at a therapeutic dose for at least six weeks in duration. Across the trials, approximately 33% to 40% of randomized patients had previously failed four or more antidepressants.18 Patients from all phase III trials had severe depression (MADRS greater than 34) at baseline (Janssen Inc.: personal communication, 2019 Feb 1).18
All the completed phase III trials, with the exception of SUSTAIN 1, included a four-week screening period prior to randomization. This screening period allowed for the inclusion of patients who had previously failed one antidepressant to be randomized in the trial if they also demonstrated nonresponse to a second antidepressant treatment during the screening phase.
Patients were specifically excluded from any of the five studies if they had MDD with psychotic features, had previously demonstrated nonresponse to ketamine in the current depressive episode, had a history of suicidal ideations in the past six months, or had a history of a substance or alcohol use disorder. In trials with elderly patients (i.e., TRANSFORM-3, SUSTAIN 2), additional exclusion criteria included a Mini-Mental State Examination score of less than 25, neurodegenerative disorders, or clinically significant cardiovascular disorders.
Table 1: Summary of Esketamine Phase III Trials — Patient and Trial Characteristics
|Name of Study||Study Details||Population||Intervention(s), Comparator(s)a||Outcomes|
|Completed, Unpublished Trials|
|Randomized, double-blind, active-controlled, multi-centre study
4-week treatment, 24-week follow-up or entry in SUSTAIN-1
N = 346
|Adults (18 to 64 years)
MDD: recurrent or single-episode (≥ 2 years), IDS-C30 ≥ 34
|Intervention: Esketamine 56 mg (n = 117) or 84 mg (n = 116) intranasally twice per week
Comparator: Matching placebo given intranasally twice per week (n = 113)
Trial ID: NCT0241858522
|Randomized, double-blind, active-controlled, multi-centre study
4-week treatment, 24-week follow-up or entry in SUSTAIN 1
N = 227 (N completing study = 197)
|Adults (18 to 64 years)
MDD: recurrent or single-episode (≥ 2 years), IDS-C30 ≥ 34
|Intervention: Esketamine 56 mg or 84 mg intranasally twice per week (n = 114)c
Comparator: Matching intranasal placebo (n = 109)
Trial ID: NCT0242218623
|Randomized, double-blind, active-controlled, multi-centre study
4-week treatment, 24-week follow-up or entry into SUSTAIN 2
N = 138
|Adults ≥ 65 years
MDD: recurrent or single-episode (≥ 2 years), IDS-C30 ≥ 31
|Intervention: Esketamine 28 mg, 54 mg, or 84 mg intranasally twice per week (n = 72)c
Comparator: Matching intranasal placebo (n = 65)
EQ-5D-5L Response rate at week 4, remission rate at week 4
|ESKETINTRD3003 (SUSTAIN 1)
Trial ID: NCT0249386824
|Active-controlled, multi-centre study (N = 705)
Direct-entry participants: uncontrolled, open-label, flexible dosing induction and optimization phase (4 weeks) (N = 437)
Transferred-entry participants: double-blind optimization (12 weeks) (N = 268)
Randomized, double-blinded, maintenance phase (N = 705)
Up to 104 weeks
|Induction/Optimization Phase: adults (18 to 64 years) with MDD: recurrent or single-episode (≥ 2 years), IDS-C30 ≥ 34, TRDb
Stable responderse from ESKETINTRD3002 and ESKETINTRD3001 at the end of 4 weeks
Maintenance phase: patients in stable remissionf or stable responsee
|Intervention: Induction (for direct-entry participants only): esketamine 56 mg or 84 mg intranasally twice per week for 4 weeks
Optimization: intranasal esketamine (same as induction) once every week for 4 weeks, then once every week or every other week
Maintenance: intranasal esketamine once every week or every other week (n = 152)
Comparator: matching intranasal placebo (n = 145)
|Time to relapse MADRS
|ESKETINTRD3004 (SUSTAIN 2)
Trial ID: NCT0249728720
|Uncontrolled, open-label, multi-centre study
Up to 52 weeks
N = 802
|Adults (≥18 years)
MDD: recurrent or single-episode (≥ 2 years), MADRS ≥ 22
Patients from ESKETINTRD3005 (regardless of their response status)
|Intervention: Induction: esketamine 28 (for ≥ 65 years old), 56 mg or 84 mg intranasally twice per week
Optimization and Maintenance: intranasal esketamine once every week or every other week
|BPIC-SS Cogstate domains and HVLT-R withdrawal symptoms (assessed by PWC-20)|
Trial ID: NCT0343404131
|Randomized, double-blind, active-controlled, multi-centre study
N = 234
|Adults (18 to 64 years)
MDD: recurrent or single-episode (≥ 2 years), MADRS ≥ 28
|Intervention: Esketamine 56 mg or 84 mg intranasally twice per week
Comparator: Matching placebo given intranasally twice per week
Onset of clinical response; response rate at week 4; remission rate at week 4; sustained remission at week 8
|54135419TRD3008 (SUSTAIN 3)
Trial ID: NCT0278210430
|Uncontrolled, open-label, long-term extension study
Up to 63 months
N = 1,150
|Patients from ESKETINTRD3001, ESKETINTRD3002, ESKETINTRD3003, ESKETINTRD3005, and ESKETINTRD3006 (US sites only)||Intervention: Induction: esketamine 24 mg, 56 mg, or 84 mg intranasally twice per week for 4 weeks
Optimization: esketamine intranasally once weekly (same dose as induction) for 4 weeks
Maintenance: esketamine intranasally once weekly or once every other week
|TEAE Blood pressure, heart rate, blood oxygen saturation, ECG, MOAAS score Computerized Cognitive Battery Domain HVLT-R C-SSRS
Time to discharge (using CGADR)
BPIC-SS = bladder pain/interstitial cystitis symptom score; C = clinician rating; CGADR = clinical global assessment of discharge readiness; CGI-S = clinical global impression – severity; C-SSRS = Columbia-Suicide Severity Rating Scale; ECG = electrocardiogram; EQ-5D-5L = EuroQol 5-Dimension 5-Levels questionnaire; GAD-7 = Generalized Anxiety Disorder 7-item scale; HVLT-R = Hopkins Verbal Learning Test‒Revised; ID = identification; IDS = Inventory of Depressive Symptomatology; MADRS = Montgomery-Åsberg Depression Rating Scale; MOAAS = Modified Observer's Assessment of Alertness/Sedation scale; PHQ-9 = Patient Health Questionnaire‒9; PWC-20 = Physician Withdrawal Checklist; SDS = Sheehan Disability Scale; TEAE = treatment-emergent adverse events; TRD = treatment-resistant depression.
a All patients in both the intervention and comparator groups also received one of the following newly initiated, open-label, oral antidepressants: duloxetine 60 mg orally daily, escitalopram 10 mg to 20 mg orally daily, sertraline 50 mg to 200 mg orally daily, or venlafaxine XR 75 mg to 225 mg orally daily.
b TRD was defined as nonresponse (≤ 25% improvement) to two to six oral antidepressants in the current episode of depression, at an adequate dose for at least six weeks in duration.
c Approximately two-thirds of patients received esketamine 84 mg and one-third received esketamine 54 mg.18
d TRD was defined as nonresponse (≤ 25% improvement) to two to nine oral antidepressants in the current episode of depression, at an adequate dose for at least six weeks in duration.
e ≥ 50% reduction in MADRS score.
f MADRS ≤ 12.
The results of the phase III trials are summarized here and depicted in Tables 2 and 3. These results have not yet been fully published; the data were obtained from conference poster presentations and an FDA briefing report (Janssen Inc.: personal communication, 2019 Feb 1).18
MADRS: This metric describes depression severity. MADRS is a clinician-rated scale consisting of 10 domains (i.e., apparent sadness, reported sadness, inner tension, sleep, appetite, concentration, lassitude, interest level, pessimistic thoughts, and suicidal thoughts), for a total possible score of 60. Higher scores indicate more severe depression and thus a decrease in scores indicate improvement. In the TRANSFORM-2 study, esketamine plus a newly initiated oral antidepressant demonstrated a statistically significant superior change in the MADRS score at day 28 (mean difference ‒4.0, 95% CI: ‒7.31 to ‒0.64; P = 0.010) relative to placebo plus a newly initiated oral antidepressant. Furthermore, the mean difference between treatment groups was statistically significant for almost all the time points throughout the 28 days of treatment. In the TRANSFORM-1 and TRANSFORM-3 trials, there was no statistically significant difference between esketamine and placebo.
Response Rates: In the TRANSFORM-1 and TRANSFORM-2 trials with participants between 18 to 64 years of age, 53.1% to 69.3% of patients who received esketamine in combination with a new oral antidepressant were stable responders (i.e., defined as 50% or higher reductions in MADRS depression severity scores) by day 28. In comparison, 38.9% to 52% of patients who received placebo with a newly initiated antidepressant were stable responders. In the TRANSFORM-3 trial with elderly participants (65years-old or more), the response rate was 27.0% in the esketamine plus antidepressant group compared with 13.3% in the group receiving placebo plus a new antidepressant.
Remission Rates: In the TRANSFORM-1 and TRANSFORM-2 trials, remission rates (i.e., defined as a MADRS score of 12 or less) ranged from 36.0% to 52.5% in the esketamine plus antidepressant group compared with 31% of patients in the placebo plus antidepressant group. As with the response rates, remission rates were lower in the elderly patients studied in the TRANSFORM-3 trial: 17.5% for the esketamine plus antidepressant group versus 6.7% for the placebo plus antidepressant group. No statistical tests were reported.
Table 2: Summary of Key Efficacy Outcomes From Four of the Phase III Trials
|Esk 56 mg||Esk 84 mg||PL||Eska||PL||Eskb||PL|
|Mean (SD) change from baseline to day 28||‒19.0 (13.86)||‒18.8 (14.12)||‒14.8 (15.07)||‒21.4 (12.32)||‒17.0 (13.88)||‒10.0 (12.74)||‒6.3 (8.86)|
|Difference of LSM (95% CI)||‒4.1 (‒7.67 to -0.49)||‒3.2 (‒6.88 to 0.45)||N/A||‒4.0 (‒7.31 to ‒0.64)||N/A||‒3.6 (‒7.20 to 0.07)||N/A|
|P value on difference||N/Ac||0.088d||N/A||0.010d||0.029e|
|Responsef at day 28|
|n (%)||60 (54.1)||52 (53.1)||42 (38.9)||70 (69.3)||52 (52.0)||17 (27.0)||8 (13.3)|
|Remissiong at day 28|
|n (%)||40 (36.0)||38 (38.8)||33 (30.6)||53 (52.5)||31 (31.0)||11 (17.5)||63 (6.7)|
CI = confidence interval; Esk = esketamine plus newly initiated oral antidepressant; IND = induction phase; LSM = least squares means; N/A = not applicable; MADRS = Montgomery-Åsberg Depression Rating Scale; PL = placebo nasal spray plus newly initiated oral antidepressant; SD = standard deviation.
a Includes 54 mg and 84 mg doses.
b Includes 24 mg, 54 mg, and 84 mg doses.
c Due to pre-defined statistical testing sequence, since the esketamine 84 mg group was non-significant, the esketamine 54 mg group could not be evaluated.
d 2-sided P value.
e 1-sided P value.
f Clinical response was defined as ≥ 50% MADRS improvement.
g Remission was defined as MADRS ≤ 12.
Source: Janssen Inc.: personal communication, 2019 Feb 1).
Results From SUSTAIN 1 (ESKETINTRD3003): A Relapse Prevention Study
A relapse event was defined as at least two MADRS scores of 22 or greater within five to 15 days, or hospitalization for worsening depression, suicide attempt, suicide prevention, or completed suicide. According to the FDA, esketamine plus a newly initiated oral antidepressant statistically significantly delayed a relapse event, compared with placebo plus antidepressant, for both stable remitters (i.e., defined as 50% or higher reductions in MADRS score) and stable responders (i.e., defined as a MADRS score of 12 or less).18 The largest differences in relapse time between treatment groups occurred within the first two to four weeks. Esketamine also statistically significantly reduced the hazard for relapse for stable remitters (HR 0.49; 95% CI: 0.29 to 0.84, P = 0.003) and for stable responders (HR 0.30; 95% CI: 0.16 to 0.55, P < 0.001). Other efficacy outcomes data are summarized in Table 3.
Table 3: Efficacy Outcomes From the Maintenance Phase of SUSTAIN 1
|Stable Remitters||Stable Responders|
|Esketamine (n = 90)||PL (n = 86)||Esketamine (n = 62)||PL (n = 59)|
|Median treatment duration (weeks)||17.7||10.2||19.4||10.1|
|Patients experiencing a relapse event (n, %)||24 (26.7)||39 (45.3)||16 (25.8)||34 (57.6)|
|Median time to relapse, days (95% CI)||NEa||273.0 (97.0 to NE)||635.0 (264.0 to 635.0)||88.0 (46.0 to 196.0)|
|Hazard ratio (95% CI)||0.49 (0.29 to 0.84)||N/A||0.30 (0.16 to 0.55)||N/A|
|2-sided P value on HR||0.003||N/A||< 0.001||N/A|
CI = confidence interval; HR = hazard ratio; NE = not estimable; PL = placebo nasal spray.
a 50% relapse rate not reached based on Kaplan–Meier estimates.
Source: Janssen Inc.: personal communication, 2019 Feb 1; FDA briefing document.18
Safety information for the completed phase III trials are reported here and in Table 2. As study results have not yet been fully published, the data were obtained from conference poster presentations and an FDA briefing report (Janssen Inc.: personal communication, 2019 Feb 1).18 An ongoing, open-label extension study is evaluating the safety of esketamine over five years following the completion of the earlier phase III efficacy trials; no results have been posted to date.30
Two (0.3%) deaths occurred in the optimization and maintenance phase of the SUSTAIN 2 trial — one due to acute respiratory and cardiac failure, and the second due to completed suicide (Janssen Inc.: personal communication, 2019 Feb 1). The FDA reports six deaths with esketamine during the development program; however, five of these deaths occurred after the drug was stopped.18 Three of these deaths were due to completed suicide, and three were due to one of following: a motor vehicle accident, sudden death, and a heart attack.
For patients in the esketamine treatment group, the frequency of serious adverse events ranged from 3.9% to 6.9%. Serious adverse events in the placebo group were only reported in TRANSFORM-3 (3.1%). These included:
- In TRANSFORM-3, three patients in the esketamine group reported anxiety, blood pressure increase, and hip fracture. Two patients in the placebo group reported feelings of despair and dizziness.
- In SUSTAIN 1, five patients reported one of the following adverse events: disorientation, hypothermia, lacunar stroke, sedation, and suicidal ideation; and one patient reported autonomic nervous system imbalance and simple partial seizure.
- In SUSTAIN 2 — a longer-term, open-label safety study that followed participants for up to one year — 55 patients reported 68 serious adverse events, with the most common events occurring in greater than two patients including depression, suicidal ideation, suicide attempt, nephritis, anxiety, and gastroenteritis. Of these serious adverse events, five were considered related to esketamine — anxiety, delusion, delirium, suicidal ideation, and suicidal attempt.
Across the phase III trials, a total of 71% to 90% of patients receiving esketamine experienced an adverse event. The frequency of adverse events in the comparator group was only reported in the TRANSFORM-3 trial as 60%. Adverse events most frequently reported included dizziness, nausea, dissociation, headache, vertigo, sedation, increased blood pressure, dysgeusia (altered sense of taste), hypoesthesia (reduced sense of touch), vomiting, and viral upper respiratory tract infection. Overall, these adverse events were less common in elderly patients than in adult patients. Blood pressure elevations, dissociative symptoms, and sedation occurred more often in the esketamine treatment group. These adverse events all occurred rapidly after receiving a dose of esketamine, peaked around 40 minutes, and resolved within four hours, 1.5 hours, and one hour, respectively. With subsequent esketamine dosing, the severity of dissociative symptoms appeared to lessen. No cases of psychosis, or ulcerative or interstitial cystitis, were reported.
The long-term safety study SUSTAIN 2 also reported moderate-to-severe nasal symptoms (e.g., taste disturbance, postnasal drip) in 11% of patients. In this study, 8.1% of patients experienced a urinary tract infection and 10.5% of all patients reported one the following urinary adverse events: dysuria (painful urination), pollakiuria (frequent daytime urination), micturition (frequent urination), urgency, and bladder pain. This safety study also reported that, regardless of age, cognitive functioning (e.g., memory, processing speed) remained stable throughout treatment.
In three of the phase III trials, discontinuation of esketamine due to adverse events ranged from 2.6% to 9.5% in the esketamine treatment group and 2.1% to 3.1% in the comparator group. The specific reasons for stopping treatment were not reported. Withdrawal due to adverse events was not reported for two of the studies.
Table 4: Number of Patients With Adverse Events in the Phase III Trials
|NoP (%): Adverse Events|
|TRANSFORM-3||51 (70.8)||39 (60.0)|
|SUSTAIN 2||723 (90.1)||N/A|
|NoP (%): Serious Adverse Events|
|TRANSFORM-3||3 (4.2)||2 (3.1)|
|SUSTAIN 1||6 (3.9)||NR|
|SUSTAIN 2||55 (6.9)||N/A|
|NoP (%): Withdrawal Due to Adverse Events|
|4 (5.6) 1 (1.4)||2 (3.1) 1 (1.5)|
|4 (2.6) NR||3 (2.1) NR|
|76 (9.5) 33 (4.1)||N/A N/A|
NoP = number of patients; NR = not reported; N/A = not applicable.
Source: Janssen Inc.: personal communication, 2019 Feb 1.
One major limitation of the evidence base presented in this bulletin is that all results were obtained from an FDA briefing report and unpublished conference posters that are not peer-reviewed and may include data gaps. Secondly, for most outcomes, the statistical significance was not calculated and it is unclear whether observed differences are clinically meaningful. Furthermore, the overall number of withdrawals in the long-term safety study was quite high, which could introduce bias to the results. In the induction phase, 198 (25.4%) patients withdrew, and of the 603 patients who entered the optimization and maintenance phase, 120 patients discontinued prior to study completion. Dissociation symptoms are a prominent side effect known to be associated with esketamine. These symptoms could have served as a cue to indicate to patients that they had received the drug, thus compromising the blinding of treatment allocation in the randomized trials.
Because of the trial design and choice of comparator, this evidence cannot be used to assess how esketamine compares with other options available to patients with TRD, such as adjunctive therapy. The generalizability of the study findings may also be limited because of the exclusion of patients with MDD with psychotic features.
Other Drugs for Treatment-Resistant Depression
Orally administered ketamine has recently been investigated for TRD in a phase I proof-of-concept study.34 In this study, oral ketamine decreased depressive symptoms and was well-tolerated.
In addition to ketamine and esketamine, there are several other compounds in development for TRD:
- Rapastinel (GLYX-13, Allergan) is a weak agonist of the NMDA receptor being investigated in phase III trials for monotherapy in TRD.35,36 It received Breakthrough Therapy designation from the FDA in 2016.7
- AXS-05 (Axsome) is a combination of dextromethorphan and bupropion that received Fast Track designation from the FDA for TRD in 2017.37 It is currently being investigated in a phase III trial for TRD.38
- Cariprazine is an atypical antipsychotic drug being investigated in a phase III trial for TRD.39,40 Of note, results from an earlier phase III trial did not demonstrate cariprazine to be superior to placebo.7
- Psilocybin is a mushroom alkaloid that binds to serotonin receptors. It was investigated in a phase II trial for TRD, which demonstrated preliminary efficacy and safety.41,42
- AVP-923 (Nuedexta, Avanir) and AVP-786 are combinations of dextromethorphan and quinidine, and being investigated in phase II trials for TRD.43,44
- AV-101 (4-chlorokynurenine, 4-Cl-KYN, VistaGen Therapeutics) acts as an antagonist of the NMDA receptor and is being investigated in phase II trials for TRD.45,46
- Minocycline is a tetracycline antibiotic with potential anti-inflammatory and neuroprotective benefits, and is being investigated in a phase II47 and phase IV48 trial for TRD.
- Sirukumab and tocilizumab, monoclonal antibodies that bind respectively interleukin-6 and its receptor, are being investigated for TRD in phase II trials.49,50
- Tulrampator (CX-1632, RespireRx) is an orally administered drug that acts on the AMPA receptor. It is being investigated in a phase II trial for TRD.51
Other Esketamine Indications
In addition to TRD, intranasal esketamine is being investigated in phase III trials for patients with MDD who are at imminent risk for suicide.52-54 Suicide remains a significant global burden, accounting for 1.5% of worldwide mortality.55 This indication received a breakthrough designation from the FDA in 2016. Results of a double-blind, randomized phase II trial comparing esketamine 84 mg with placebo twice weekly demonstrated statistically significant improvements in suicidal thoughts within four hours; however, these effects were not sustained at 24 hrs.54 Similarly, esketamine statistically significantly improved depressive symptoms at four hours and approximately 24 hours; however, these effects were not sustained at day 25.
Inhaled esketamine is also being investigated in a phase II study for treatment-resistant bipolar depression.56
Cited concerns surrounding intravenous ketamine for depression may inform potential uptake issues for esketamine. One key concern with ketamine is its safety profile, specifically dissociative and cognitive side effects, sedation, elevations in blood pressure, and toxicity to the urinary system.57 With the exception of cognitive dysfunction, these side effects were also reported with intranasal esketamine use (Janssen Inc.: personal communication, 2019 Feb 1). However, the majority of the urinary adverse events were mild and resolved without intervention. Dissociative symptoms, blood pressure elevations, and sedation were reported to resolve within a few hours but may require patient monitoring shortly after drug administration. Ketamine’s potential for addiction and diversion was another important concern.57 However, post-marketing data suggests that ketamine abuse is in fact relatively uncommon.18 Much like ketamine, esketamine has psychotogenic properties that also make it susceptible to abuse; risk management could still be an important consideration.7,16,58
Cautions currently exist surrounding driving after receiving ketamine, given the potential for dissociative and sedative side effects.18,57 A small, double-blind, randomized phase I study assessed esketamine’s impact on driving performance.59 Healthy patients received single doses of esketamine 84 mg intranasally, oral placebo, and mirtazapine 30 mg orally in a crossover design. There were no statistically significant differences between esketamine and placebo groups in their driving performance (i.e., measured by the weaving of a car) eight hours after drug administration, whereas mirtazapine had a significant detrimental impact on driving relative to placebo. However, the generalizability of these results to chronic esketamine use is limited. Given the prevalence of dissociation and sedation in the larger phase III trials, the risk for potential accidents and the impact on driving may still be of concern.
Although esketamine is formulated in a more convenient nasal spray device, it must be administered under direct medical supervision. This could present a challenge for patients, as it would require repeat visits to the physician’s office on a bi-weekly basis. Because of the potential driving impairment shortly after esketamine administration, travelling to the physician’s clinic and back may be problematic for patients, especially in areas with limited public transportation. The need for medical supervision also poses the question of organizing the distribution of this drug in Canada: if patients are required to obtain the medication at their retail pharmacy, policies may be required to ensure that the patient does not self-administer the medication.
There is also the potential for off-label use, as esketamine is being investigated for not only unipolar TRD but also for depression with imminent risk of suicide and treatment-resistant bipolar depression. There is also the risk of off-label use for patients with non‒treatment-resistant MDD.
While there are ongoing long-term safety studies, further research is required to inform the appropriate duration of esketamine treatment and whether it can eventually be tapered or discontinued. Furthermore, there is a lack of evidence comparing intranasal esketamine to current adjunctive strategies for TRD.
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About this Document
Authors: Bryanna Nicole Tibensky, Louis de Léséleuc, Christine Perras, Lory Picheca
Cite As: Esketamine for Treatment-Resistant Depression. Ottawa: CADTH; 2019 April. (CADTH issues in emerging health technologies; issue 176).
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