Clinical Study Evaluating Effects of Pharmacogenetic-guided vs Standard-of-Care Treatment on Depression and/or Anxiety

Sponsor

AltheaDx (Industry)

Overall Status

Completed

CT.gov ID

NCT02878928

Collaborator

Innovis LLC (Industry)

579

Enrollment

Locations

Arms

Duration (Months)

34.1

Patients Per Site

4.8

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

A prospective, multi-center, randomized, subject and outcome evaluator blind , parallel-group study evaluating the effect of pharmacogenetic-guided versus standard of care treatment for subjects diagnosed with depression and/or anxiety disorders.

Condition or Disease	Intervention/Treatment	Phase
Depression Anxiety	Genetic: IDgenetix Neuropsychiatric Test Panel	N/A

Detailed Description

A substantial number of patients taking anti-depressant and anti-anxiety medications suffer from either a lack of benefit from drug therapy or severe side effects. Clinical features often fail to predict the drug response and tolerability of a patient to a prescription medication. Genetics can help guide therapeutic decisions for patients exhibiting neuropsychiatric disorders and potentially improve patient outcomes by maximizing drug efficacy and minimizing the risk of adverse events. Genetics and drug interactions can alter both the pharmacokinetics and pharmacodynamics of a multitude of drug compounds and in turn influence both the safety and efficacy of selected therapeutic regimens.

This study is designed to evaluate the clinical impact of pharmacogenetic (PGx)-directed treatment. Pharmacogenetic-guided therapy selection using the IDgenetix Neuropsychiatric Test Panel can enhance patient response and tolerability by facilitating the selection of the most appropriate medication at the most effective dose in the shortest possible time.

In this prospective, multi-center, randomized, subject and outcome evaluator blind, parallel-group study patients presenting to the clinical site with evidence of depression and/or anxiety as determined by a qualified clinician will be invited to participate. Study participants will be randomized to one of two groups with respect to the IDgenetix Neuropsychiatric Test Panel result: group with testing results revealed to the medical provider prior to treatment selection (Experimental Group) or group without testing results prior to treatment selection (Control Group). Participant outcomes will be measured at baseline and throughout the 3-month duration of the study.

Study Design

Study Type:

Interventional

Actual Enrollment :

579 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Double (Participant, Outcomes Assessor)

Primary Purpose:

Diagnostic

Official Title:

A Prospective, Multi-Center, Randomized Clinical Study to Evaluate the Clinical Impact of Pharmacogenetic-Guided Treatment for Depression & Anxiety

Study Start Date :

May 1, 2016

Actual Primary Completion Date :

Dec 1, 2016

Actual Study Completion Date :

Dec 1, 2016

Arms and Interventions

Arm	Intervention/Treatment
Experimental: IDgenetix Neuropsychiatric Test Panel Intervention Medical providers for IDgenetix Neuropsychiatric Test Panel-guided group will make treatment recommendations based on test results. Patient outcomes will be measured throughout the duration of the study.	Genetic: IDgenetix Neuropsychiatric Test Panel The IDgenetix Neuropsychiatric Test Panel is used to make recommendations on the medication therapy that might be impacted by the genetic background of the patient. Other Names: PGx Testing
No Intervention: Control Group Medical providers for the Control Group will not receive IDgenetix Neuropsychiatric Test Panel results and will make treatment recommendations as usual. Patient outcomes will be measured throughout the duration of the study.

Arm

Intervention/Treatment

Experimental: IDgenetix Neuropsychiatric Test Panel Intervention

Medical providers for IDgenetix Neuropsychiatric Test Panel-guided group will make treatment recommendations based on test results. Patient outcomes will be measured throughout the duration of the study.

Genetic: IDgenetix Neuropsychiatric Test Panel

The IDgenetix Neuropsychiatric Test Panel is used to make recommendations on the medication therapy that might be impacted by the genetic background of the patient.

Other Names:

PGx Testing

No Intervention: Control Group

Medical providers for the Control Group will not receive IDgenetix Neuropsychiatric Test Panel results and will make treatment recommendations as usual. Patient outcomes will be measured throughout the duration of the study.

Outcome Measures

Primary Outcome Measures

The reduction of adverse drug events (ADE) subsequent to pharmacogenetics-guided treatment as compared to standard of care for treatment of depression and/or anxiety symptoms. [12 weeks]

Secondary Outcome Measures

Change in the Hamilton Rating Scale for Depression (HAMD-17) score from baseline. [12 weeks]
Change in the Hamilton Rating Scale for Anxiety (HAM-A) score from baseline. [12 weeks]
Percentage of depression subjects who respond (≥50% decrease in HAM-D17 from baseline or remit, HAM-D17 total score ≤7). [12 weeks]
Percentage of anxiety subjects who respond (≥50% decrease in HAM-A from baseline or remit, HAM-A total score ≤7) [12 weeks]
Time to response/remission of depressive symptoms. [12 weeks]
Time to response/remission of anxiety symptoms. [12 weeks]
Medication change: Number of subjects who changed their antidepressant and anxiety medication regimens from baseline. [12 weeks]
The impact of pharmacogenetic-guided treatment.care costs as measured by HMWDQ [12 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male or female subjects 18 years of age or older.
Subjects diagnosed with depression and/or anxiety as per the DSM-V criteria or standard of care site procedures and meeting at least one of the following:
Diagnosed with depression and/or anxiety either new to treatment or currently taking medications for less than 6 weeks.
Inadequately controlled with medications defined as inadequate efficacy after 6 weeks of a psychotropic treatment or have discontinued psychotropic treatment due to adverse events or intolerability.
Willing and able to comply with study procedures.
Able to provide written informed consent.

Exclusion Criteria

Unwilling or unable to provide written informed consent and to comply with study procedures.
Any patient for whom providing a buccal swab sample would be contraindicated or not possible.
Subjects diagnosed as not having anxiety or depression.
Patients at significant risk for suicide and/or in need of immediate hospitalization as judged by the investigator.
Diagnosis of Bipolar Disorder, as assessed by patient history or M.I.N.I. response.
Diagnosis of Schizophrenia or Schizoaffective disorder, as assessed by patient history or M.I.N.I. response.
History or diagnosis of a personality disorder, as assessed by patient history or M.I.N.I. response.
History of physical traumatic injury (i.e., TBI) resulting in depression.
Patients new to psychotherapy (provided by licensed and trained mental health professionals) or have not been on a stable psychotherapy regimen for at least 8 weeks.
Patients receiving other alternative treatments such as Electroconvulsive Therapy (ECT), Transcranial Magnetic Stimulation (TMS), Vagal Nerve Stimulation (VNS), and Deep Brain Stimulation (DBS).
Patients with a history of chronic renal dysfunction, Chronic Kidney Disease (Stage 4 or 5).
Patients with abnormal hepatic function within the last 2 years, (INR >1.2 not attributable to anticoagulant medications, AST/aspartate aminotransferase or ALT/alanine aminotransferase >1.5x normal, or suspected cirrhosis).
Patients with a history of malabsorption (short gut syndrome).
Patients with any gastric or small bowel surgery less than 3 months prior to study enrollment.
Patients with significant unstable medical condition, neurological disorders (e.g. epilepsy, Parkinson's disease or stroke) or life threatening disease.
Patients who are currently being treated for anxiety and /or depression incorporating pharmacogenetic information.
History of hypothyroidism unless taking a stable dose of thyroid medication and asymptomatic for 6 months.
Patients with any significant substance use disorder as assessed by M.I.N.I. response and judged by the investigator.
Pregnant or lactating women.

Contacts and Locations

Locations

	Site	City	State	Country
1	Adnab Research	Rolling Hills	California	United States
2	Artemis Clinical Research	San Diego	California	United States
3	Adnab Research	Torrance	California	United States
4	Collaborative Neuroscience Network	Torrance	California	United States
5	Innovative Clinical Research	Lauderhill	Florida	United States
6	Innova Clinical Trials	Miami	Florida	United States
7	APG Research	Orlando	Florida	United States
8	iResearch Atlanta	Decatur	Georgia	United States
9	Meridian Clinical Research	Savannah	Georgia	United States
10	Medpharmics	Metairie	Louisiana	United States
11	Meridian Clinical Research	Norfolk	Nebraska	United States
12	United Medical Associates	Binghamton	New York	United States
13	Richmond Behavioral Associates	Staten Island	New York	United States
14	Carolina Partners in Mental HealthCare	Raleigh	North Carolina	United States
15	Detweiler Family Medicine	Lansdale	Pennsylvania	United States
16	Relaro Medical Trials	Dallas	Texas	United States
17	Tidewater Clinical Research	Virginia Beach	Virginia	United States