Substance P Antagonist in the Treatment of Posttraumatic Stress Disorder
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|ClinicalTrials.gov Identifier: NCT00383786|
Recruitment Status : Completed
First Posted : October 4, 2006
Results First Posted : January 31, 2014
Last Update Posted : February 13, 2018
This study, conducted at the NIH and the Mount Sinai School of Medicine, will examine the effectiveness of a substance P or NK1 antagonist study drug known as GR205171 in treating the symptoms of posttraumatic stress disorder (PTSD).
People between 18 and 65 years of age who have been diagnosed with PTSD may be eligible for this study. Participants undergo the following tests and procedures:
Treatment: Patients are tapered off current ineffective medications over 1 to 2 weeks. All participants receive placebo (sugar pill) at the start of the study. At some point within the first 3 weeks of the study, they are then randomly assigned either to take GR205171 or to continue with placebo for the remainder of the 10-week treatment period.
Clinic visits: Patients come to the clinic once a week during treatment. The following procedures are done at various visits.
- Interviews, self report questionnaires and psychiatric rating scales at every visit.
- Physical examination, blood and urine tests. Blood is drawn up to 10 times during the study.
Follow-up visits continue for up to 3 months after the end of the study, during which patients are offered standard clinical treatment.
|Condition or disease||Intervention/treatment||Phase|
|PTSD||Drug: NK1 Antagoist (GR205171) Procedure: Psychophysiology (Trauma Script) Procedure: Psychophysiology (Verbal Threat) Procedure: Psychophysiology (Fear Conditioning) Procedure: Psychophysiology (Affective Modulation) Procedure: Psychophysiology (Heart rate variability) Procedure: Lumbar Puncture Procedure: 24-hour plasma sampling Procedure: MRI||Phase 2|
Posttraumatic Stress Disorder (PTSD) is a common chronic anxiety disorder that is often debilitating and follows exposure to an overwhelming traumatic event. The burden of PTSD on individuals and society is significant. The majority of PTSD sufferers also meet the diagnostic criteria for several other psychiatric disorders and many attempt suicide. Despite the devastating impact of PTSD on the lives of millions worldwide, little is known about the etiology or pathophysiology of this disorder. Although disruptions in the hypothalamic-pituitary adrenal (HPA) Axis, noradrenergic, serotonergic systems have been proposed as neurobiological substrates in the development of PTSD, the exact underpinnings of the neurobiology of PTSD remain to be fully elucidated.
PTSD is responsive to treatment with selective serotonin reuptake inhibitors, but response rates rarely exceed 60%, and even fewer patients (20%-30%) experience improvement that could be characterized as remission. Thus, there is a clear need to develop novel and improved therapeutics for PTSD. A growing body of preclinical evidence suggests that activation of the Substance P (SP) and its receptor NK1 is anxiogenic and that NK1 antagonists, upon chronic administration, exert significant dampening (albeit complex) effects on the SP-NP system. Furthermore, several stress paradigms are believed to exert many of their deleterious effects on hippocampal structures via enhancement of SP-NK1 system. Overall, excess activity of the SP-NK1 system stands as a prime candidate for involvement in the pathophysiology of anxiety disorders such as PTSD.
In this study, we propose to investigate the potential antianxiety efficacy of the highly specific NK1 antagonist GR205171 in PTSD. Furthermore, we propose to, in a preliminary fashion, longitudinally investigate whether neuroendocrine surrogate markers are predictive of treatment response.
This is an 8-week double-blind placebo-controlled study that will examine the efficacy and safety of an NK1 antagonist in patients with PTSD.
Patients, ages 18 to 65 years with a diagnosis of PTSD, will in this pilot study be randomized to double-blind treatment to receive either the NK1 antagonist, GR205171 (5 mg/day) or placebo for a period of 8 weeks.
Approximately 52 patients will enter the study to obtain 40 subjects who complete the 8 weeks of acute NK1 antagonist treatment.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||47 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Investigator)|
|Official Title:||Evaluation of the Efficacy of the NK1 Antagonist GR205171 in Posttraumatic Stress Disorder|
|Study Start Date :||September 2006|
|Primary Completion Date :||June 2009|
|Study Completion Date :||June 2009|
selective neurokinin-1 receptor antagonist, fixed 5 mg dose every day, for 8 weeks.
|Drug: NK1 Antagoist (GR205171) Procedure: Psychophysiology (Trauma Script) Procedure: Psychophysiology (Verbal Threat) Procedure: Psychophysiology (Fear Conditioning) Procedure: Psychophysiology (Affective Modulation) Procedure: Psychophysiology (Heart rate variability) Procedure: Lumbar Puncture Procedure: 24-hour plasma sampling Procedure: MRI|
Placebo Comparator: placebo
|Procedure: Psychophysiology (Trauma Script) Procedure: Psychophysiology (Verbal Threat) Procedure: Psychophysiology (Fear Conditioning) Procedure: Psychophysiology (Affective Modulation) Procedure: Psychophysiology (Heart rate variability) Procedure: Lumbar Puncture Procedure: 24-hour plasma sampling Procedure: MRI|
- Changes in CAPS Scores. [ Time Frame: Baseline, 8 weeks ]The Clinician-Administered PTSD Scale (CAPS) is the gold standard in PTSD assessment. The CAPS is a 30-item structured interview that corresponds to the DSM-IV criteria for PTSD. This is a 17-item core symptom scale, measuring both frequency and intensity of symptoms, with the most frequently used scoring rule is to count a symptom as present if it has a frequency of 1 or more and an intensity of 2 or more. A PTSD diagnosis is made if there is at least 1 "B" symptom, 3 "C" symptoms, and 2 "D" symptoms as well as meeting the other diagnostic criteria. Scores range from 0-136 0 (best possible outcome) to 136 (worst possible outcome). The relevant time-points for reporting change were at baseline and 8 weeks.
- Able to Identify Biological Markers That Predict Response to Treatment. [ Time Frame: 10 weeks ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00383786
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike|
|Bethesda, Maryland, United States, 20892|
|United States, New York|
|Mt. Sinai Medical Center|
|New York, New York, United States, 10029-0574|
|Principal Investigator:||Dennis S Charney, MD||Icahn School of Medicine at Mount Sinai|