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Linagliptin in Schizophrenia Patients

Primary Purpose

Schizophrenia

Status
Terminated
Phase
Phase 1
Locations
Malaysia
Study Type
Interventional
Intervention
Linagliptin
Sponsored by
Monash University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years of age and above
  • Diagnosis of schizophrenia.
  • Clinically stable antipsychotic regimen for the last 3 months
  • A total score of 80 or greater at baseline on the Positive and Negative Syndrome Scale
  • Competent and willing to provide written, informed consent

Exclusion Criteria:

  • History of substance dependence within the past 2 months
  • Existing relevant physical health problems: such as uncontrolled cardiovascular disease and impaired liver/ renal function
  • History of diabetes
  • History of hepatic or biliary diseases / biliary obstruction
  • A serious suicide/homicide risk in the opinion of the investigator
  • Known allergy to linagliptin

Sites / Locations

  • Pusat Perubatan Universiti Kebangsaan Malaysia

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Linagliptin

Arm Description

Linagliptin daily

Outcomes

Primary Outcome Measures

PANSS Score

Secondary Outcome Measures

Drug safety
No of adverse events recorded per patients

Full Information

First Posted
August 22, 2013
Last Updated
August 14, 2018
Sponsor
Monash University
Collaborators
Universiti Kebangsaan Malaysia Medical Centre
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1. Study Identification

Unique Protocol Identification Number
NCT01943019
Brief Title
Linagliptin in Schizophrenia Patients
Official Title
A Pilot Study to Assess the Efficacy of Linagliptin as an Adjunct in Schizophrenia Patients
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Terminated
Why Stopped
Inability to obtain patients
Study Start Date
August 2013 (undefined)
Primary Completion Date
July 2018 (Actual)
Study Completion Date
August 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Monash University
Collaborators
Universiti Kebangsaan Malaysia Medical Centre

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Approximately one third of patients with schizophrenia show a poor response to standard treatment with antipsychotic medications. This treatment resistant group of patients represents a major challenge in everyday psychiatry, and consumes a disproportionate amount of time from the clinicians, resulting in considerable costs to the society and government. Anecdotal evidence suggests that the enzyme dipeptidyl peptidase IV (DPPIV) may be altered in patients with schizophrenia, with a higher level DPPIV enzyme activity being noted. We postulate that this may play a role in the neuropathology of schizophrenia patients and by inhibiting the DPPIV enzyme activity with a DPPIV inhibitor such as linagliptin, we will be able to improve and even ameliorate the symptoms of schizophrenic patients. However, until now there have yet any studies on the potential of these inhibitors in schizophrenia patients. A pilot study is thus proposed to evaluate the potential of the DPPIV inhibitor, linagliptin as an adjunct in schizophrenia patients who are non-responsive to treatment, which will establish the feasibility of a larger trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Linagliptin
Arm Type
Experimental
Arm Description
Linagliptin daily
Intervention Type
Drug
Intervention Name(s)
Linagliptin
Primary Outcome Measure Information:
Title
PANSS Score
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Drug safety
Description
No of adverse events recorded per patients
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
DPP-4 enzyme levels
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age and above Diagnosis of schizophrenia. Clinically stable antipsychotic regimen for the last 3 months A total score of 80 or greater at baseline on the Positive and Negative Syndrome Scale Competent and willing to provide written, informed consent Exclusion Criteria: History of substance dependence within the past 2 months Existing relevant physical health problems: such as uncontrolled cardiovascular disease and impaired liver/ renal function History of diabetes History of hepatic or biliary diseases / biliary obstruction A serious suicide/homicide risk in the opinion of the investigator Known allergy to linagliptin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maniam Thambu
Organizational Affiliation
Pusat Perubatan UKM
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pusat Perubatan Universiti Kebangsaan Malaysia
City
Bandar Tun Razak
State/Province
Kuala Lumpur
ZIP/Postal Code
56000
Country
Malaysia

12. IPD Sharing Statement

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Linagliptin in Schizophrenia Patients

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