Trial Outcomes & Findings for Targeting IL-17A for Treatment-Resistant Depression (NCT NCT04979910)

NCT ID: NCT04979910

Last Updated: 2025-05-20

Results Overview

The safety and feasibility of using ixekizumab in patients with TRD will be assessed by the completion of treatment measured as the receipt of all three Ixekizumab injections (160 mg at week 0, 80 mg at weeks 2 and 4). Drop-out rates will be calculated.

Recruitment status

COMPLETED

Study phase

PHASE2

Target enrollment

7 participants

Primary outcome timeframe

6 weeks

Results posted on

2025-05-20

Participant Flow

Participant milestones

Participant milestones
Measure
Ixekizumab
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Overall Study
STARTED
7
Overall Study
COMPLETED
7
Overall Study
NOT COMPLETED
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Targeting IL-17A for Treatment-Resistant Depression

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Age, Continuous
45.29 years
STANDARD_DEVIATION 17.57 • n=99 Participants
Sex: Female, Male
Female
5 Participants
n=99 Participants
Sex: Female, Male
Male
2 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
6 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=99 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=99 Participants
Race (NIH/OMB)
Asian
1 Participants
n=99 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=99 Participants
Race (NIH/OMB)
Black or African American
0 Participants
n=99 Participants
Race (NIH/OMB)
White
5 Participants
n=99 Participants
Race (NIH/OMB)
More than one race
1 Participants
n=99 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=99 Participants

PRIMARY outcome

Timeframe: 6 weeks

The safety and feasibility of using ixekizumab in patients with TRD will be assessed by the completion of treatment measured as the receipt of all three Ixekizumab injections (160 mg at week 0, 80 mg at weeks 2 and 4). Drop-out rates will be calculated.

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Number of Participants Who Dropped-out
0 Participants

PRIMARY outcome

Timeframe: 6 weeks

The incidence and frequency of all anticipated and unanticipated serious and non-serious adverse events

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Number of Anticipated and Unanticipated Adverse Events
8 events

SECONDARY outcome

Timeframe: Baseline and 6 weeks

Response rate at week 6 as compared to baseline, defined as \>=50% MADRS total score improvement. The Montgomery-Åsberg Depression Rating Scale (MADARS) is a 10-item instrument used for the evaluation of depressive symptoms in adults and for the assessment of any changes to those symptoms. Each of the 10 items is rated on a scale of 0 to 6, with differing descriptors for each item. These individual item scores are added together to form a total score, which can range between 0 and 60 points. The MADRS provides a measure of the overall level of depression. Higher score indicates poorer health outcome.

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Change in Montgomery-Åsberg Depression Rating Scale Score - Response Rate
Baseline
28.57 score on a scale
Standard Deviation 6.55
Change in Montgomery-Åsberg Depression Rating Scale Score - Response Rate
6 weeks
23.86 score on a scale
Standard Deviation 10.07

SECONDARY outcome

Timeframe: Baseline and 6 weeks

Remission rate at week 6 as compared to baseline, defined as MADRS total score of \<=10.. The Montgomery-Åsberg Depression Rating Scale (MADARS) is a 10-item instrument used for the evaluation of depressive symptoms in adults and for the assessment of any changes to those symptoms. Each of the 10 items is rated on a scale of 0 to 6, with differing descriptors for each item. These individual item scores are added together to form a total score, which can range between 0 and 60 points. The MADRS provides a measure of the overall level of depression. Higher score indicates poorer health outcome.

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Change in Montgomery-Åsberg Depression Rating Scale Score - Remission Rate
baseline
28.57 score on a scale
Standard Deviation 6.55
Change in Montgomery-Åsberg Depression Rating Scale Score - Remission Rate
6 weeks
23.86 score on a scale
Standard Deviation 10.07

SECONDARY outcome

Timeframe: Baseline and 6 weeks

The Quick Inventory of Depressive Symptomatology, Self-Report (QIDS-SR) is a 16-item self-rated instrument designed to assess the severity of depressive symptoms. The 16 items cover the nine symptom domains of major depression and are rated on a scale of 0-3. Total score ranges from 0 to 27, with ranges of 0-5 (normal), 6-10 (mild), 11-15 (moderate), 16-20 (moderate to severe), and 21+ (severe). Higher score indicates poorer health outcome.

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Change in Quick Inventory of Depressive Symptomatology, Self-Report [QIDS-SR] Score
baseline
13.57 score on a scale
Standard Deviation 4.04
Change in Quick Inventory of Depressive Symptomatology, Self-Report [QIDS-SR] Score
6 weeks
11.57 score on a scale
Standard Deviation 5.50

SECONDARY outcome

Timeframe: Up to Week 6

The Snaith-Hamilton Pleasure Scale (SHAPS) is a well-validated 14-item self-report questionnaire commonly used to assess anhedonia. Each item on the SHAPS is worded so that higher scores indicate greater pleasure capacity. A total score can be derived by summing the responses to each item. Items answered with "strongly agree" are coded as "1", while a "strongly disagree" response was assigned a score of "4." Total scores on the SHAPS can range from 14 to 56, with higher scores corresponding to higher levels of anhedonia.

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Change in Snaith-Hamilton Pleasure Scale (SHAPS)
baseline
35.29 score on a scale
Standard Deviation 11.43
Change in Snaith-Hamilton Pleasure Scale (SHAPS)
6 weeks
33.14 score on a scale
Standard Deviation 12.23

SECONDARY outcome

Timeframe: Baseline and 6 weeks

The Temporal Experience of Pleasure Scale (TEPS) is an 18-item self-report measurement of anhedonia which consists of a series of statements that must be rated according to how accurate they are for the individual. The scale produces a sub-score that differentiates the role of anticipatory pleasure ('wanting') and is derived of 10 items. Subscales scores from 9-54. Total scores range is 16-108. Lower scores indicate greater levels of anhedonia.

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Change in Temporal Experience of Pleasure Scale
baseline
57.71 score on a scale
Standard Deviation 21.78
Change in Temporal Experience of Pleasure Scale
6 weeks
63.14 score on a scale
Standard Deviation 24.59

SECONDARY outcome

Timeframe: Baseline and 6 weeks

This is a widely administered clinician rated scale that assesses the subject overall illness severity and the degree of improvement from the initial assessment. Illness severity is rated on a 1-7 scale where 1 corresponds to "Normal, Not at All Ill", 2 is "Borderline Mentally Ill", the anchor for 3 is "Mildly Ill", the anchor for 4 is "Moderately Ill", 5 is "Markedly Ill", 6 is "Severely Ill", and 7 is "Among the Most Extremely Ill Patients". Illness improvement is rated on a 1-7 scale where 1 corresponds to "Very Much Improved", 2 is "Much Improved", the anchor for 3 is "Minimally Improved", the anchor for 4 is "No Change", 5 is "Minimally Worse", 6 is "Much Worse", and 7 is "Very Much Worse".

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Change in Clinical Global Impression Scale
Baseline CGI - Improvement
3.43 score on a scale
Standard Deviation 1.51
Change in Clinical Global Impression Scale
6 weeks - Improvement
3.57 score on a scale
Standard Deviation 0.98
Change in Clinical Global Impression Scale
baseline - Severity
4.71 score on a scale
Standard Deviation 0.49
Change in Clinical Global Impression Scale
6 weeks - Severity
4.29 score on a scale
Standard Deviation 0.76

SECONDARY outcome

Timeframe: Baseline and 6 weeks

The Columbia-Suicide Severity Rating Scale (C-SSRS) is a comprehensive, semi-structured interview that uniquely measures the full spectrum of suicidality including passive and active suicidal ideation, suicidal intent as well as suicidal behaviors. Full range from 0 to 9, with higher score indicating higher suicidal ideation severity.

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Change in The Columbia-Suicide Severity Rating Scale (C-SSRS)
Baseline
0.86 score on a scale
Standard Deviation 1.21
Change in The Columbia-Suicide Severity Rating Scale (C-SSRS)
6 weeks
0.57 score on a scale
Standard Deviation 1.13

SECONDARY outcome

Timeframe: Baseline and 6 weeks

The Hamilton Anxiety Rating Scale (HAM-A) is a scale of assessments of anxiety states. The scale consists of 14 items, each defined by a series of symptoms, and measures both psychic anxiety (mental agitation and psychological distress) and somatic anxiety (physical complaints related to anxiety). Each item is scored on a scale of 0 (not present) to 4 (severe), with a total score range of 0-56, where \<17 indicates mild severity, 18-24 mild to moderate severity and 25-30 moderate to severe. Higher score indicates poorer health outcomes.

Outcome measures

Outcome measures
Measure
Ixekizumab
n=7 Participants
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Change in The Hamilton Anxiety Rating Scale (HAM-A)
baseline
19.00 score on a scale
Standard Deviation 5.57
Change in The Hamilton Anxiety Rating Scale (HAM-A)
6 weeks
14.86 score on a scale
Standard Deviation 7.01

Adverse Events

Ixekizumab

Serious events: 0 serious events
Other events: 4 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Other adverse events
Measure
Ixekizumab
n=7 participants at risk
Ixekizumab 160 mg (two 80 mg injections) at Week 0, followed by 80 mg at Weeks 2 and 4 via subcutaneous route. Ixekizumab: a monoclonal antibody (mAb) against interleukin 17A (IL-17A)
Nervous system disorders
Headache
14.3%
1/7 • 6 weeks
Gastrointestinal disorders
Nausea
14.3%
1/7 • 6 weeks
Nervous system disorders
Tinnitus
14.3%
1/7 • 6 weeks
Musculoskeletal and connective tissue disorders
Myalgia
14.3%
1/7 • 6 weeks
Nervous system disorders
Hot Flashes
14.3%
1/7 • 6 weeks
Gastrointestinal disorders
Bloating
14.3%
1/7 • 6 weeks
Cardiac disorders
Palpitation
14.3%
1/7 • 6 weeks
Skin and subcutaneous tissue disorders
Skin Lesion
14.3%
1/7 • 6 weeks

Additional Information

Esther Lee

Icahn School of Medicine at Mount Sinai

Phone: 212-585-6133

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place