Evaluating the Efficacy of Adjunctive Minocycline for the Treatment of Bipolar Depression
Information source: University Health Network, Toronto
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Bipolar Disorder; Bipolar Depression; Bipolar I Depression; Bipolar II Depression
Intervention: Minocycline (Drug)
Phase: Phase 3
Status: Recruiting
Sponsored by: University Health Network, Toronto Official(s) and/or principal investigator(s): Roger S McIntyre, MD, FRCPC, Principal Investigator, Affiliation: University Health Network, Toronto
Summary
Long-term studies have emphasized that depressive symptoms and episodes account for majority
of the illness burden experienced by individuals with bipolar disorder (BD). Previous
studies have shown that blood levels of proteins called pro-inflammatory cytokines are
abnormal in individuals with bipolar depression. The investigators hypothesize that
preventing the production or release of pro-inflammatory cytokines will result in
improvement of depressive symptoms in individuals with bipolar depression. Minocycline is a
medication that inhibits the activation of immune cells (i. e. microglia) in the brain and
reduces the production of pro-inflammatory cytokines. Treatment with minocycline has been
shown to have antidepressant-like effects in animal studies and improve symptoms of
individuals with schizophrenia. In this study, minocycline (100 mg twice a day) will be
administered for 8 weeks to determine if it is an efficacious antidepressant for individuals
with bipolar depression.
Clinical Details
Official title: A Pilot, Open-label, 8-Week Study Evaluating the Efficacy, Safety, and Tolerability of Adjunctive Minocycline for the Treatment of Bipolar Depression
Study design: Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Change from baseline to week 8 on the Montgomery Asberg Depression Rating Scale (MADRS)
Secondary outcome: Change from baseline to week 8 on the Hamilton Depression Rating Scale 17-item (HAMD-17)Change from baseline to week 8 on the Somatic Symptom Inventory (SSI) Change from baseline to week 8 on the Clinical Global Impression (CGI) Rating Scale Change from baseline to week 8 in the in neurocognitive function Monitoring of Side-effects from baseline to week 8 with the Toronto Side Effect Scale (TSES) Monitoring of suicide severity from baseline to week 8 with the Columbia Suicide Severity Rating Scale (C-SSRS). Change from baseline to week 8 in concentrations of pro-and anti-inflammatory cytokines (i.e. TNFα, IL-1β, IL-2, IL-6, IL8, IFNγ, IL-4, IL-5, IL-10)
Detailed description:
Bipolar disorder (BD) is associated with a high-rate of non-recovery, recurrence, and
inter-episodic dysfunction. Depressive symptoms and episodes dominate the longitudinal
course of BD and differentially account for overall illness burden. During the past decade,
substantial developments have been made in the pharmacological and psychosocial treatment of
bipolar mania and maintenance, with relatively few treatments proven efficacious for bipolar
depression. The absence of an explanatory disease model in bipolar disorder has limited the
development and evaluation of genuinely novel agents for bipolar disorder.
Several lines of evidence implicate the inflammatory system as consequential and causative
to mood disorder. Bipolar disorder is marked by alterations in inflammatory cytokines (e. g.
TNF-alpha, IL-6). Moreover, pro-inflammatory activation in both healthy and medically ill
individuals is associated with disturbances in affective, cognitive, and somatic function.
The clinical use of cytokine-based therapy has been demonstrated to induce and/or intensify
affective symptomatology in non-psychiatric medical patients. Conventional pharmacological
treatments (e. g. lithium) for bipolar disorder affects the production of pro-inflammatory
cytokines as well as their gene expression. The encompassing aim of the study herein is to
develop a novel treatment for bipolar depression based on a model of disease
pathophysiology. Minocycline is a semisynthetic second-generation tetracycline, which exerts
anti-inflammatory effects that are distinct from its antimicrobial properties.
Minocycline is a potent inhibitor of microglial activation and decreases expression of
pro-inflammatory cytokines, chemokines and their receptors and suppresses the activity of
matrix metalloproteinases. Minocycline has been shown to exert antidepressant-like
properties in preclinical studies. Rats treated with minocycline monotherapy as well as
combination treatment with an antidepressant (desipramine) exhibited significantly improved
performance on the forced swim test. Adjunctive minocycline has been shown to be efficacious
for the treatment of schizophrenia in a double-blind, randomized, placebo-controlled study.
Subjects receiving minocycline exhibited a significant improvement in negative symptoms as
well as global improvement as measured with the Clinical Global Impression (CGI).
Significant improvement was also noted on measures of executive function, including
executive function composite score, spatial recognition memory, cognitive planning, and
intradimensional/extradimensional set shifting.
A total of 40 individuals between the ages of 18 and 65 meeting DSM-IV-TR criteria for a
current major depressive episode as part of bipolar I or II disorder will be enrolled into
an 8-week, open-label study with adjunctive minocycline (100 mg every 12 hours).
Eligibility
Minimum age: 18 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Diagnosis of bipolar I or II disorder
- Meets criteria for a current major depressive episode
- A score of >= 20 on the HAMD-17 at the time of enrollment and at baseline
- Episode duration will be greater than 4 weeks but not longer than 12 months.
Exclusion Criteria:
- Insufficiently responding to >2 treatment strategies FDA/Health
Canada-approved/guideline recommended for bipolar depression
- Acute manic or mixed episode
- An Axis I psychiatric disorder requiring primary clinical attention
- Clinically significant medical illness
- Treatment with minocycline or β-lactam antibiotics in the preceding 6 months
- Hypersensitivity to minocycline or any other tetracycline
- Physical injury requiring medical treatment or surgery in the last 6 months
- Pregnant or breast-feeding
- Inability to provide written informed consent.
Locations and Contacts
University Health Network, Toronto, Ontario M5T 2S8, Canada; Recruiting Joanna K Soczynska, HBSc, PhD Candidate, Phone: (416) 603-5800, Ext: 3726, Email: joanna.soczynska@uhn.ca Hanna O Woldeyohannes, HBSc, Phone: (416) 603-5133, Email: hanna.woldeyohannes@uhn.ca Roger S McIntyre, MD, FRCPC, Principal Investigator
Additional Information
Related publications: Levkovitz Y, Mendlovich S, Riwkes S, Braw Y, Levkovitch-Verbin H, Gal G, Fennig S, Treves I, Kron S. A double-blind, randomized study of minocycline for the treatment of negative and cognitive symptoms in early-phase schizophrenia. J Clin Psychiatry. 2010 Feb;71(2):138-49. doi: 10.4088/JCP.08m04666yel. Epub 2009 Nov 3. Molina-Hernández M, Tellez-Alcántara NP, Pérez-García J, Olivera-Lopez JI, Jaramillo-Jaimes MT. Antidepressant-like actions of minocycline combined with several glutamate antagonists. Prog Neuropsychopharmacol Biol Psychiatry. 2008 Feb 15;32(2):380-6. Epub 2007 Sep 14.
Starting date: July 2011
Last updated: July 25, 2011
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