Study of ABX-002 for the Adjunctive Treatment of Major Depressive Disorder (AMPLIFY)

Official title

A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study of ABX-002 for the Adjunctive Treatment of Major Depressive Disorder

Overview

The goal of this clinical trial is to learn if ABX-002 added to an existing antidepressant treatment will benefit depression symptoms in adults with moderate to severe major depressive disorder who have had an inadequate response to their antidepressant. This is a double-blind, placebo-controlled, 2-arm, parallel-group, Phase 2 study, randomized 1:1 (ABX-002: placebo). The study will include the following stages: 1. Screening, approximately 35 days 2. 42-day Treatment Period 3. 2-week post dose Safety Follow-up Period 4. 6-month postdose targeted safety follow-up period

Interventions

• Drug ABX-002
  ABX-002 oral solution in 1-mL cyclic olefin polymer prefilled syringes, taken on an empty stomach first thing in the morning followed by 240 mL (8 oz) of water.
• Other Placebo
  Comparator Placebo oral solution in 1-mL cyclic olefin polymer prefilled syringes, taken on an empty stomach first thing in the morning followed by 240 mL (8 oz) of water.

Primary outcome measures

• Change from Baseline in the 17-item Hamilton Rating Scale for Depression (HAMD-17) [Time frame: 6 weeks]

Secondary outcome measures (6)

• Change from Baseline for Clinical Global Impression of Severity (CGI-S) [Time frame: 6 weeks]
• Change from Baseline for Sheehan Disability Scale (SDS) [Time frame: 6 weeks]
• Change from baseline for 6-item Hamilton Rating Scale for Depression (HAMD-6) [Time frame: 6 weeks]
• Change from baseline for 29-item Hamilton Rating Scale for Depression (HAMD-29) [Time frame: 6 weeks]
• Patient Global Impression-Improvement (PGI-I) [Time frame: 6 weeks]
• Assessment of safety and tolerability of ABX-002 compared with placebo using adverse events [Time frame: 6 weeks]

Eligibility criteria

Inclusion criteria

• Meets the DSM-5 criteria for Major Depressive Disorder, with a current major depressive episode duration of > 6 weeks and ≤ 18 months.
• A score of ≤ 22 (midrange mild/moderate) on the Hamilton Anxiety Rating Scale.
• Montgomery-Asberg Depression Rating Scale total score of > 24 \[indicating moderate to severe depression\] at Screening and at Baseline.
• Subject is compliantly using a single selective serotonin reuptake inhibitors / serotonin norepinephrine reuptake inhibitor antidepressant for at least 6 weeks for their current episode of depression, with an adequate dose, and with an inadequate response as defined by the Antidepressant Treatment Response Questionnaire. The dosage of the current antidepressant must have been stable for the past 4 weeks, and the dosage and specific antidepressant used should remain the same from Screening through the end of the Follow-up Period.

Exclusion criteria

Note: History implies lifetime history, unless otherwise specified

• History of schizophrenia or other psychotic disorder, major depressive disorder with psychotic features or concomitant DSM-5 depressive disorders, bipolar I or II disorder, cyclothymic disorder, delirium, dementia, amnestic disorder, or cognitive disorder.
• Current diagnosis or active symptoms within the last 2 years of obsessive-compulsive disorder, posttraumatic stress disorder, panic disorder, or eating disorder, according to DSM-5 criteria.
• Primary diagnosis of borderline, antisocial, paranoid, schizoid, schizotypal, or histrionic personality disorder, according to DSM-5 criteria. Current or history within the last 2 years of self-injurious behavior is exclusionary.
• Has failed more than 2 single selective serotonin reuptake inhibitors / serotonin norepinephrine reuptake inhibitor antidepressant treatments, including the current serotonin reuptake inhibitors / serotonin norepinephrine reuptake inhibitor, during the current depressive episode, despite an adequate dose (per Antidepressant Treatment Response Questionnaire) and duration (at least 6 weeks).
• Failure to respond to triiodothyronine or thyroxine augmentation for the treatment of depression.
• Started new psychotherapy or had a change in the intensity of psychotherapy within 8 weeks before Screening.
• Is suicidal at Screening or Baseline
• History or current evidence within previous 3 months before Screening of uncontrolled, clinically significant neurological, gastrointestinal, respiratory, renal, hepatic, immunological, hematological, or other medical disorder, including cancer, that would jeopardize the safe participation of the subject in the study (in the opinion of the Investigator).
• History of thyroid disease
• History of multiple endocrine neoplasia syndrome
• Diagnosis of epilepsy or history of convulsions, including childhood febrile seizure. Use of co-administered drugs that may lower seizure threshold is excluded.
• Females who are pregnant, intend to become pregnant or are breastfeeding.
• Antidepressants: Prior use of psychedelics, ketamine, or esketamine, for the treatment of Major Depressive Disorder.
• Antidepressants: Current use, or use within 4 weeks prior to Screening, of any other augmentation agents for Major Depressive Disorder (e.g. second-generation antipsychotics \[SGA\], monoamine oxidase inhibitors \[MAOI\], tricyclic antidepressants \[TCA\], lithium, or bupropion)
• Current or prior use of treatment for hypothyroidism including but not limited to synthetic or natural thyroid hormone, triiodothyronine and/or thyroxine.
• Concomitant use of biotin of any dose and in any preparation 14 days prior to Day 1 until after the last study visit at Week 8 (Day 56).
• Medications that are strong cytochrome P450 3A4 inhibitors or strong cytochrome P450 3A4 inducers are not allowed.
• Prescription drug/controlled substance abuse, or illicit substance use within 1 year of Screening or positive urine drug results at Screening or Baseline for an illicit substance.
• History or presence of cataract on ophthalmic examination (including slit-lamp), glaucoma, inflammatory eye disease or prior ophthalmic surgical procedures or laser surgery in either eye

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Double blind

Primary purpose

Treatment

Study locations

United States · 50 centers

• Autobahn Site #131 — Birmingham
• Autobahn Site #132 — Chandler
• Autobahn Site #116 — Phoenix
• Autobahn Site #136 — Tucson
• Autobahn Site #150 — Anaheim
• Autobahn Site #113 — Encino
• Autobahn Site #133 — Encino
• Autobahn Site #124 — Glendale
• … and 42 more centers

Identifiers

NCT: NCT06633016 · ABX-002-2001

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗