Cysteamine Therapy for Major Depressive Disorder

Major Depressive Disorder Clinical Trial

Official title:

An Open-Label Study of Cysteamine Bitartrate in Treatment-Resistant Major Depression

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00715559
• Other study ID #: GCO # 07-0478
• Status: Terminated
• Phase: N/A
• First received: July 11, 2008
• Last updated: April 5, 2017
• Start date: July 2008
• Est. completion date: May 2009

Study information

• Verified date: April 2017
• Source: Icahn School of Medicine at Mount Sinai
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether cysteamine bitartrate, an FDA-approved drug for a non-psychiatric condition, is safe and effective for the treatment of major depression.

Description:

Major depressive disorder (MDD) is a chronic, disabling illness affecting about 17% of the general population. Despite advances in treatment, about two-thirds of patients fail to respond to an initial trial of pharmacotherapy. Brain-derived neurotrophic factor (BDNF) is a neural growth-promoting polypeptide found in the central nervous system, and has been implicated in the pathophysiology and potential treatment of MDD. A multitude of studies have shown low levels of BDNF in subjects with MDD, which have normalized after treatment with an antidepressant. Traditional antidepressants such as serotonin reuptake inhibitors may increase BDNF via an indirect intracellular pathway. The current study drug, cysteamine bitartrate (Cystagon), is FDA approved for the treatment nephropathic cystinosis and has been shown to increase BNDF in neuronal tissue, and to stimulate cell growth. Cysteamine has already been investigated in humans as a potential treatment for Huntington's Disease. Given the evidence of decreased levels in major depression, and subsequent increase post-treatment with antidepressants, BDNF may play a key role in developing novel treatments for patients who have failed conventional agents. Therefore, drugs that can demonstrably increase central BDNF, such as cysteamine, may have significant potential as novel antidepressant medications.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 3
• Est. completion date: May 2009
• Est. primary completion date: May 2009
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Male or female patients, 21-65 years of age.

2. Female subjects who are not of childbearing potential (i.e., surgically sterile, postmenopausal for at least one year) or must be using a medically accepted means of contraception. Women using oral contraceptive medication for birth control must also be using a barrier contraceptive. Women of childbearing potential must also have a negative serum B-HCG at pre-study.

3. Subjects must fulfill DSM-IV criteria for Major Depression without psychotic features, based on clinical assessment by a study psychiatrist and confirmed by a structured diagnostic interview, the Structured Clinical Interview for DSM-IV TR Axis I Disorders, (SCID-P).

4. Subjects have a history of at least one previous episode of depression prior to the current episode (recurrent major depressive disorder) or have chronic major depressive disorder (at least two years' duration).

5. Subjects have not responded to an adequate trial of one antidepressant in the current episode as determined by Antidepressant Treatment History Form (ATHF) criteria (score > 3) (Sackeim 2001)

6. Subjects must have an initial score of ³ 32 on the IDS-C at both Visit 1 and Visit 2.

7. Each subject must have a level of understanding sufficient to agree to all tests and examinations required by the protocol and must sign an informed consent document.

8. Current major depressive episode is of at least 4 weeks duration

Exclusion Criteria:

1. Presence of psychotic features, diagnosis of schizophrenia or any other psychotic disorder, or bipolar disorder/cyclothymia as defined in the DSM-IV.

2. Lifetime histories of autism, mental retardation, pervasive developmental disorders, OCD, or Tourette's

3. Current Eating Disorder

4. Subjects with a history of DSM-IV drug or alcohol dependency or abuse (except for nicotine or caffeine) within the preceding 3 months.

5. Female subjects who are either pregnant or nursing.

6. Serious, unstable illnesses including hepatic, renal, respiratory, cardiovascular (including ischemic heart disease), endocrinologic, neurologic (including history of severe head injury), immunologic, or hematologic disease.

7. Hypersensitivity to cysteamine or penicillamine

8. Past history of severe gastrointestinal disease (including peptic ulcers or inflammatory bowel disease), or current gastroesophageal reflux disease

9. Subjects with a history of neutropenia or medication-induced blood dyscrasia.

10. Clinically significant abnormal findings of laboratory parameters, physical examination, or ECG.

11. Subjects with uncorrected hypothyroidism or hyperthyroidism.

12. Subjects with one or more seizures without a clear and resolved etiology.

13. Treatment with a reversible MAOI within 2 weeks prior to Visit 2.

14. Treatment with fluoxetine within 4 weeks prior to Visit 2.

15. Treatment with any other concomitant medication not allowed 14 days prior to study Visit 2.

16. Treatment with clozapine or ECT within 3 months prior to study Visit 2.

17. Judged clinically to be at serious suicidal or homicidal risk.

18. Participation in a clinical trial of another investigational drug within 1 month prior to study entry.

19. Patients starting hormonal treatment (e.g., estrogen) in the last 3 months prior to visit 1.

20. Psychotherapy or nonpharmacological antidepressant treatments (e.g. light therapy

Related Conditions & MeSH terms

• Depression
• Depressive Disorder
• Depressive Disorder, Major
• Major Depressive Disorder

Intervention

Drug:
• cysteamine bitartrate
All enrolled participants will begin open treatment with cysteamine on the first visit of the experimental period (after screening, medical clearance and medication washout period if necessary). The dosing schedule is a flexible regimen starting at 150 mg PO three times daily. After one week, patients without intolerable side effects will increase the dose to 300 mg three times daily. The titration schedule will continue up to a maximum of 1800 mg a day. In case of adverse events, the investigator may decrease the dose by 150 mg daily.

Locations

Country	Name	City	State
United States	Mount Sinai School of Medicine	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Icahn School of Medicine at Mount Sinai

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Montgomery-Åsberg Depression Rating Scale (MADRS)	This scale measures depression severity. It ranges from a score of 0 to 60, with higher score indicating higher level of depression severity.	8 weeks
Secondary	Clinical Global Impression Scales for Severity (CGI-S) and Improvement (CGI-I)	This set of scales measures "global" improvement in a patient's level of symptoms, without reference to a particular condition (ie depression). GCI-S is a measure of severity, which ranges from 0 (not ill) to 7 (severely ill). CGI-I is a measure of change, with a score of 4 indicating no change, 1 indicating very much improved and 7 indicating very much worse.	8 weeks
Secondary	Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR16)	This is a self-report which measures the level of depression severity. I ranges from 0 (no illness) to 27 (severe illness).	8 weeks
Secondary	Systematic Assessment for Treatment Emergent Effects (SAFTEE)	The SAFTEE is used to measure somatic and other symptoms which may arise during the course of a clinical trial. This is a non-quantitative instrument that does not yield a numeric score. Instead, it provides study subjects the opportunity to check off symptoms listed on a checklist and indicate if the severity of the symptoms is "mild" "moderate" or "severe." The reported values represent symptoms that were indicated at any point during the 8 week trial at a level of "moderate" or "severe" that also represented a change from a baseline-line pre-intervention SAFTEE assessment.	weekly, for 8 weeks