Nepicastat for Posttraumatic Stress Disorder (PTSD) in OIF/OEF Veterans

NCT ID: NCT00659230

Last Updated: 2017-10-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-07-01
• Study Completion Date: 2012-08-30

Brief Summary

This study proposes a multi-site, randomized, double-blind, placebo-controlled clinical trial of the dopamine-ß-hydroxylase (DBH) inhibitor, nepicastat, for the treatment of posttraumatic stress disorder (PTSD) in outpatients who have previously served in a combat zone during Operation Iraqi Freedom and Operation Enduring Freedom (OIF/OEF)or other Southwest conditions since 19800. A DBH inhibitor's mechanism of action is to decrease neuronal noradrenaline (NA) release by inhibiting DBH conversion of dopamine (DA) to NA. Animal models of PTSD and human studies have found a substantial increase in NA activity for these animal models and for PTSD in humans. Furthermore, recent clinical studies have improved PTSD hyper-arousal symptoms by reducing the NA over-activity using agents like NA post-synaptic antagonists. Key support for the proposed study is based on a similar improvement in PTSD symptoms after treatment with the DBH inhibitor, disulfiram.

In the experience of the clinical investigators, the most common chief complaint of the OIF/OEF veterans with PTSD is hyperarousal (DSM-IV criterion D symptom cluster). These symptoms significantly interfere with social, occupational, and interpersonal function. Standard treatments with antidepressants are not fully effective in treating the symptoms of PTSD in veterans; thus, new treatments are needed. An intervention, such as nepicastat, aimed at reducing hyperarousal, as well as other PTSD symptoms, would have significant impact of restoring overall function and quality of life in OIF/OEF veterans with PTSD. Since hyperarousal symptoms responded relatively quickly to medications of this type, our study in 120 outpatient veterans with PTSD will compare nepicastat 120 mg/day vs. placebo in a 6-week double-blind, randomized clinical trial (RCT). The veterans will be followed for an additional 8 weeks after the RCT, during which, those who have a priori defined positive clinical response to the study medication, nepicastat vs. placebo, will be continued on the study medication, in order to assess further improvement and safety. Those patients who do not have a positive clinical response during the 6 week RCT will be offered the addition of the standard first-line PTSD pharmacotherapy, paroxetine, during the 8 weeks extension phase. Thus, weeks 7-14 offer an opportunity to evaluate longer-term nepicastat efficacy and to compare the treatment response of nonresponders after augmentation with paroxetine.

Detailed Description

HYPOTHESES Primary Hypothesis: Compared to placebo treatment, nepicastat-treated OIF/OEF veterans with PTSD will have significantly reduced PTSD hyperarousal symptoms as defined by the Clinician Administered PTSD Scale [CAPS], subscale D (CAPS-D).

Secondary Hypotheses: Compared to placebo, nepicastat-treated OIF/OEF veterans with PTSD will have:

• Significantly reduced PTSD symptoms (total CAPS)
• Significantly reduced PTSD reexperiencing symptoms (CAPS-B)
• Significantly reduced PTSD avoidance symptoms (CAPS-C)

Conditions

Posttraumatic Stress Disorder

Keywords

PTSD; Veterans; Nepicastat; OIF/OEF

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Placebo

Arm 1

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

100-800mg placebo

Nepicastat

Arm 2

Group Type: ACTIVE_COMPARATOR

Nepicastat

Intervention Type: DRUG

100-800mg

Interventions

Nepicastat

100-800mg

Intervention Type: DRUG

Placebo

100-800mg placebo

Intervention Type: DRUG

Other Intervention Names

SYN117; Dopamine beta hydroxylase (DBH) inhibitor

Eligibility Criteria

Inclusion Criteria

• Signed informed consent
• Patient understands the risks and benefits and agrees to visit frequency and procedures
• Male or female
• Any race or ethnic origin
• Served in OIF/OEF or Afghanistan conflicts or other Southwest Asia conditions
• Currently Active Duty, National Guard, Reservist, Veteran, and/or Retired Military
• Diagnosis of PTSD (by MINI (Mini International Neuropsychiatric Interview) and CAPS-DX (Clinician Administered PTSD scale- Diagnostic Form) using Rule of Fours and total CAPS-DX score of 45)
• No substance use disorders in the previous 2 weeks and no substance dependence disorders in the past 4 weeks (except for nicotine and caffeine)
• Free of psychotropic medication for 2 weeks prior to randomization
• Physical and laboratory panel are within normal limits or not clinically significant
• Women of childbearing potential must be using medically-approved methods of birth control
• ≥19 to 65 years of age

Exclusion Criteria

• Lifetime history of bipolar I, schizophrenia, schizoaffective or cognitive disorders
• Actively considering plans of suicide or homicide
• Psychotic symptoms that in the investigator's opinion impair the patient's ability to give informed consent or make it unsafe for patient to be maintained without a neuroleptic
• Unstable general medical conditions or a contraindication to the use of nepicastat
• Women planning to become pregnant or breastfeed during the study
• Current or pending incarceration
• Terminal Illness

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Acorda Therapeutics

INDUSTRY

Sponsor Role: collaborator

Ralph H. Johnson VA Medical Center

FED

Sponsor Role: collaborator

Baylor College of Medicine

OTHER

Sponsor Role: collaborator

San Diego Veterans Healthcare System

FED

Sponsor Role: collaborator

James J. Peters Veterans Affairs Medical Center

FED

Sponsor Role: collaborator

Tuscaloosa Research & Education Advancement Corporation

OTHER

Sponsor Role: lead

Responsible Party

Lori Davis, MD

Associate Chief of Staff

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Carlos Berry, M.D.

Role: STUDY_CHAIR

IRB Tuscaloosa VAMC

Locations

Tuscaloosa VAMC

Tuscaloosa, Alabama, United States

VA San Diego Healthcare System

San Diego, California, United States

James J.Peters VA Medical Center

The Bronx, New York, United States

Countries

United States

References

Kosten TR, Krystal J. Biological mechanisms in posttraumatic stress disorder. Relevance for substance abuse. Recent Dev Alcohol. 1988;6:49-68. doi: 10.1007/978-1-4615-7718-8_3.

Reference Type: BACKGROUND

PMID: 3283864 (View on PubMed)

Graham DP, Nielsen DA, Kosten TR, Davis LL, Hamner MB, Makotkine I, Yehuda R. Examining the utility of using genotype and functional biology in a clinical pharmacology trial: pilot testing dopamine beta-hydroxylase, norepinephrine, and post-traumatic stress disorder. Psychiatr Genet. 2014 Aug;24(4):181-2. doi: 10.1097/YPG.0000000000000039. No abstract available.

Reference Type: BACKGROUND

PMID: 24983834 (View on PubMed)

Other Identifiers

PT074384/W81XWH-08-2-0071

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

PT074384/W81XWH-09-1-0287

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

08-06

Identifier Type: -

Identifier Source: org_study_id