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20110165: Study to Evaluate the Effect of AMG 747 on Schizophrenia Negative Symptoms (Study 165)

Primary Purpose

Schizophrenia

Status
Terminated
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
AMG 747
Placebo
Sponsored by
Amgen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring schizophrenia negative symptoms

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) schizophrenia
  • Total score on the PANSS Marder Negative Symptom Factor Scale (NSFS) ≥ 20
  • Total score on the PANSS Marder Positive Symptom Factor Scale (PSFS) ≤ 30
  • Receiving stable antipsychotic therapy for at least 8 weeks prior to screening
  • Receiving a stable dose of other psychotropic agents for at least 8 weeks prior to screening
  • Subject has had a stable residence or living arrangement for at least 8 weeks prior to screening and the residence or living arrangement is not anticipated to change for the duration of the study
  • The subject or subject's legally acceptable representative has provided informed consent.

Exclusion Criteria:

  • Current schizoaffective or bipolar disorder, panic disorder, obsessive compulsive disorder, evidence of mental retardation by history or clinical examination or known premorbid IQ ≤ 70
  • Clinically significant suicidal ideation or suicide attempts, assaultive behavior or marked changes in mood within the 8 weeks prior to screening, or currently endorsing suicidal ideation in clinical exam
  • Substance abuse (with the exception of nicotine or caffeine abuse) within the 8 weeks prior to screening, or during screening
  • Substance dependence (with the exception of nicotine or caffeine dependence) within the 6 months prior to screening, or during screening
  • Planning to initiate a smoking cessation therapy or otherwise substantially modify nicotine use during the study
  • Positive urine drug test for substances of abuse (with the exception of positive screens for prescribed agents such as benzodiazepines).
  • Other criteria may apply

Sites / Locations

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Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

AMG 747 - Dose 1

AMG 747 - Dose 2

AMG 747 - Dose 3

Placebo Comparator

Arm Description

Outcomes

Primary Outcome Measures

Change from baseline to week 12 in negative symptoms, as measured by the NSA-16 total score
NSA-16 = 16-item Negative Symptom Assessment Scale, an efficacy scale used for the primary endpoint

Secondary Outcome Measures

Response defined as a ≥ 20% decrease in the NSA-16 total score at week 12
NSA-16 = 16-item Negative Symptom Assessment Scale
Change from baseline to week 12 on the PANSS total score and Marder factor scores
Positive and Negative Syndrome Scale (PANSS)
Change from baseline to week 12 on the CGI-S
Clinical Global Impression Severity Scale (CGI-S)
CGI-I scores at week 12
Clinical Global Impression Improvement (CGI-I)
Change on cognition battery
Change in personal and social functioning
Change on patient reported outcomes

Full Information

First Posted
February 28, 2012
Last Updated
September 19, 2014
Sponsor
Amgen
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1. Study Identification

Unique Protocol Identification Number
NCT01568229
Brief Title
20110165: Study to Evaluate the Effect of AMG 747 on Schizophrenia Negative Symptoms (Study 165)
Official Title
A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effect of Add-on AMG 747 on Schizophrenia Negative Symptoms
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Terminated
Why Stopped
Toxic Epidermal Necrolysis
Study Start Date
May 2012 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Amgen

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effect of AMG 747 on negative symptoms of schizophrenia in patients who are stable on current antipsychotic treatment. After a run-in period on their current antipsychotic treatment, patients will be randomized to one of the four treatment arms as add-on therapy for a treatment duration of up to 3 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
schizophrenia negative symptoms

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
111 (Actual)

8. Arms, Groups, and Interventions

Arm Title
AMG 747 - Dose 1
Arm Type
Experimental
Arm Title
AMG 747 - Dose 2
Arm Type
Experimental
Arm Title
AMG 747 - Dose 3
Arm Type
Experimental
Arm Title
Placebo Comparator
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
AMG 747
Intervention Description
Three dose levels once-daily oral administration
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Once-daily oral administration
Primary Outcome Measure Information:
Title
Change from baseline to week 12 in negative symptoms, as measured by the NSA-16 total score
Description
NSA-16 = 16-item Negative Symptom Assessment Scale, an efficacy scale used for the primary endpoint
Time Frame
12 Weeks
Secondary Outcome Measure Information:
Title
Response defined as a ≥ 20% decrease in the NSA-16 total score at week 12
Description
NSA-16 = 16-item Negative Symptom Assessment Scale
Time Frame
12 Weeks
Title
Change from baseline to week 12 on the PANSS total score and Marder factor scores
Description
Positive and Negative Syndrome Scale (PANSS)
Time Frame
12 weeks
Title
Change from baseline to week 12 on the CGI-S
Description
Clinical Global Impression Severity Scale (CGI-S)
Time Frame
12 weeks
Title
CGI-I scores at week 12
Description
Clinical Global Impression Improvement (CGI-I)
Time Frame
12 weeks
Title
Change on cognition battery
Time Frame
12 weeks
Title
Change in personal and social functioning
Time Frame
12 weeks
Title
Change on patient reported outcomes
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) schizophrenia Total score on the PANSS Marder Negative Symptom Factor Scale (NSFS) ≥ 20 Total score on the PANSS Marder Positive Symptom Factor Scale (PSFS) ≤ 30 Receiving stable antipsychotic therapy for at least 8 weeks prior to screening Receiving a stable dose of other psychotropic agents for at least 8 weeks prior to screening Subject has had a stable residence or living arrangement for at least 8 weeks prior to screening and the residence or living arrangement is not anticipated to change for the duration of the study The subject or subject's legally acceptable representative has provided informed consent. Exclusion Criteria: Current schizoaffective or bipolar disorder, panic disorder, obsessive compulsive disorder, evidence of mental retardation by history or clinical examination or known premorbid IQ ≤ 70 Clinically significant suicidal ideation or suicide attempts, assaultive behavior or marked changes in mood within the 8 weeks prior to screening, or currently endorsing suicidal ideation in clinical exam Substance abuse (with the exception of nicotine or caffeine abuse) within the 8 weeks prior to screening, or during screening Substance dependence (with the exception of nicotine or caffeine dependence) within the 6 months prior to screening, or during screening Planning to initiate a smoking cessation therapy or otherwise substantially modify nicotine use during the study Positive urine drug test for substances of abuse (with the exception of positive screens for prescribed agents such as benzodiazepines). Other criteria may apply
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MD
Organizational Affiliation
Amgen
Official's Role
Study Director
Facility Information:
Facility Name
Research Site
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72211
Country
United States
Facility Name
Research Site
City
Springdale
State/Province
Arkansas
ZIP/Postal Code
72764
Country
United States
Facility Name
Research Site
City
Long Beach
State/Province
California
ZIP/Postal Code
90813
Country
United States
Facility Name
Research Site
City
Oakland
State/Province
California
ZIP/Postal Code
94612
Country
United States
Facility Name
Research Site
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
Research Site
City
Hialeah
State/Province
Florida
ZIP/Postal Code
33018
Country
United States
Facility Name
Research Site
City
Kissimmee
State/Province
Florida
ZIP/Postal Code
34741
Country
United States
Facility Name
Research Site
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30328
Country
United States
Facility Name
Research Site
City
Rockville
State/Province
Maryland
ZIP/Postal Code
20850
Country
United States
Facility Name
Research Site
City
Flowood
State/Province
Mississippi
ZIP/Postal Code
39232
Country
United States
Facility Name
Research Site
City
Princeton
State/Province
New Jersey
ZIP/Postal Code
08540
Country
United States
Facility Name
Research Site
City
Buffalo
State/Province
New York
ZIP/Postal Code
14215
Country
United States
Facility Name
Research Site
City
New York
State/Province
New York
ZIP/Postal Code
10027
Country
United States
Facility Name
Research Site
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Name
Research Site
City
Scranton
State/Province
Pennsylvania
ZIP/Postal Code
18503
Country
United States
Facility Name
Research Site
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38119
Country
United States
Facility Name
Research Site
City
Dallas
State/Province
Texas
ZIP/Postal Code
75230
Country
United States
Facility Name
Research Site
City
Brno
ZIP/Postal Code
615 00
Country
Czech Republic
Facility Name
Research Site
City
Olomouc
ZIP/Postal Code
779 00
Country
Czech Republic
Facility Name
Research Site
City
Praha 2
ZIP/Postal Code
120 00
Country
Czech Republic
Facility Name
Research Site
City
Praha 9
ZIP/Postal Code
190 00
Country
Czech Republic
Facility Name
Research Site
City
Prerov
ZIP/Postal Code
750 01
Country
Czech Republic
Facility Name
Research Site
City
Strakonice
ZIP/Postal Code
386 29
Country
Czech Republic
Facility Name
Research Site
City
Créteil cedex
ZIP/Postal Code
94010
Country
France
Facility Name
Research Site
City
Dôle
ZIP/Postal Code
39100
Country
France
Facility Name
Research Site
City
Montauban cedex
ZIP/Postal Code
82013
Country
France
Facility Name
Research Site
City
Nimes
ZIP/Postal Code
30029
Country
France
Facility Name
Research Site
City
Ipoh
State/Province
Perak
ZIP/Postal Code
30450
Country
Malaysia
Facility Name
Research Site
City
Ipoh
State/Province
Perak
ZIP/Postal Code
31250
Country
Malaysia
Facility Name
Research Site
City
Kuala Lumpur
State/Province
Wilayah Persekutuan
ZIP/Postal Code
55100
Country
Malaysia
Facility Name
Research Site
City
Kuala Lumpur
State/Province
Wilayah Persekutuan
ZIP/Postal Code
56000
Country
Malaysia
Facility Name
Research Site
City
Kuala Lumpur
State/Province
Wilayah Persekutuan
ZIP/Postal Code
59100
Country
Malaysia
Facility Name
Research Site
City
Bydgoszcz
ZIP/Postal Code
85-096
Country
Poland
Facility Name
Research Site
City
Chelmno
ZIP/Postal Code
86-200
Country
Poland
Facility Name
Research Site
City
Katowice
ZIP/Postal Code
40-340
Country
Poland
Facility Name
Research Site
City
Skorzewo
ZIP/Postal Code
60-185
Country
Poland
Facility Name
Research Site
City
Torun
ZIP/Postal Code
87-100
Country
Poland
Facility Name
Research Site
City
Zuromin
ZIP/Postal Code
09-300
Country
Poland
Facility Name
Research Site
City
Barnet
ZIP/Postal Code
EN5 3DJ
Country
United Kingdom
Facility Name
Research Site
City
Edinburgh
ZIP/Postal Code
EH10 5HF
Country
United Kingdom
Facility Name
Research Site
City
London
ZIP/Postal Code
SE5 8AF
Country
United Kingdom
Facility Name
Research Site
City
Norwich
ZIP/Postal Code
NR1 3RE
Country
United Kingdom
Facility Name
Research Site
City
Sheffield
ZIP/Postal Code
S10 3TH
Country
United Kingdom
Facility Name
Research Site
City
Warrington
ZIP/Postal Code
WA2 8WA
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
27789188
Citation
Dunayevich E, Buchanan RW, Chen CY, Yang J, Nilsen J, Dietrich JM, Sun H, Marder S. Efficacy and safety of the glycine transporter type-1 inhibitor AMG 747 for the treatment of negative symptoms associated with schizophrenia. Schizophr Res. 2017 Apr;182:90-97. doi: 10.1016/j.schres.2016.10.027. Epub 2016 Oct 24.
Results Reference
derived
Links:
URL
http://www.amgentrials.com
Description
AmgenTrials clinical trials website

Learn more about this trial

20110165: Study to Evaluate the Effect of AMG 747 on Schizophrenia Negative Symptoms (Study 165)

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