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Phase IIb-III Study of BL-1020 Small Molecule for Schizophrenia (CLARITY)

Primary Purpose

Schizophrenia, Cognitive Effect on Schizophrenic Patients

Status
Terminated
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
CYP-1020
Risperidone
Sponsored by
BioLineRx, Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male or non-pregnant or lactating female, 18-50 years of age inclusive
  2. Patients must have exhibited symptoms meeting the criteria of schizophrenia for at least one year, but not more than 20 years, prior to Screening
  3. Recent onset (not more than 30 days) of worsening of psychiatric symptoms at Screening.
  4. Currently experiencing an acute exacerbation of schizophrenia, as defined by the following results at Screening and Baseline:

    • ≥70 total score on the PANSS
    • ≥4 (moderate) on two of the following four PANSS items: (1) delusions, (2) hallucinatory behaviors, (3) conceptual disorganization or (4) suspiciousness/persecution, where at least one of the two items must be either delusions or hallucinatory behaviors
  5. CGI-S score between 4 and 6 (moderately ill to severely ill) at the Screening and Baseline visits.
  6. Has exhibited a sufficient clinical response to at least one previous course of an anti-psychotic agent prescribed at a generally recognized therapeutic dose.
  7. Must have completed at least 5 years of formal education or its equivalent

Exclusion Criteria:

  1. Breastfeeding or pregnant
  2. Symptoms of schizophrenia for more than 20 years at the time of screening.
  3. Psychotic symptoms that have failed to improve (based on Investigator's opinion or documented medical history) following sufficient treatment with therapeutic doses of two or more anti-psychotics agents over the preceding 2 years
  4. Prior history of neuroleptic malignant syndrome
  5. Prior history or current evidence of moderate or severe tardive dyskinesia (mild is acceptable).
  6. Abnormal ECG evaluation
  7. History of confirmed epilepsy or prior seizure disorder (history of a single febrile seizure is not exclusionary)
  8. In the opinion of the investigator, unstable medical disease (e.g., malignancy, poorly controlled diabetes or hypertension, ischemic cardiac disease, dilated cardiomyopathy or valvular heart disease, pulmonary disease, liver disease, kidney disease)
  9. Acute infectious disease (e.g., malaria, dengue fever, hepatitis A), or chronic infectious disease (e.g., history of AIDS or HIV positivity, tuberculosis)
  10. Likely allergy, sensitivity or intolerance to BL-1020, perphenazine, risperidone, paliperidone, or any of the drug product excipients
  11. Any suicide attempt within the preceding 2 years
  12. Any Substance Dependence disorder
  13. High likelihood of substance abuse
  14. Diagnosis with one of the following DSM-IV-TR Axis I diagnoses: schizophreniform disorder, schizoaffective disorder, bipolar disorder, substance dependency, mood disorder with psychotic features; psychotic disorder NOS
  15. Requiring chronic treatment with benzodiazepines
  16. Requiring chronic treatment with mood stabilizers
  17. Previously treated with clozapine within 6 months prior to screening
  18. Any abnormal clinical laboratory test result that is judged by the Investigator to be clinically significant
  19. History of, or serologic evidence of, acute or chronic active hepatitis B or C

Sites / Locations

  • Department of Psychiatry, Sheath VS General Hospital, Sheath KM School of Post Graduate Medicine & Research
  • Saoji Tupkari Hospital
  • Spandana Nursing Home
  • KHM Hospital
  • Asha Hospital
  • Department of Psychiatry, Owaisi Hospital & Research Centre
  • RK Yadav Memorial Mental Health and De-addiction Hospital
  • Mahendru Psychiatric Centre
  • Dreamland Nursing Home
  • Dayanand Medical College & Hospital
  • Centre for Psychiatric Research, Department of Psychiatry, K.S Hegde Medical Academy
  • Jaslok Hospital&Research Centre
  • JSS Medical College Hospital
  • Sujata Birla Hospital
  • Vimhans Hospital
  • S.V.Medical College
  • Deva Mental Health Care
  • Vijayawada Institute of Mental Health & Neurosciences
  • IMSP Spitalul Clinic de Psihiatrie, Sectia 14
  • IMSP Spitalul Clinic de Psihiatrie, Sectia 17
  • IMSP Spitalul Clinic de Psihiatrie, Sectia 8
  • pitalul Clinic Judetean de Urgenta Arad Clinica Psihiatrie
  • Spitalul de Psihiatrie si Neurologie Brasov
  • Spitalul Clinic de Psihiatrie "Prof. Dr. Al. Obregia"
  • Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 13
  • Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 1
  • Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 8
  • Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 9
  • Spitalul de Psihiatrie C.E.T.T.T. "Sf. Stelian"
  • Spitalul Judetean Cluj Napoca
  • Spitalul Clinic Judetean de Urgenta Constanţa Clinica de Psihiatrie
  • Spitalul Clinic de Neuropsihiatrie Clinica de Psihiatrie nr. 2
  • Spitalul de Neuropsihiatrie Clinica de Psihiatrie I
  • Spitalul Clinic de Psihiatrie Socola
  • Spital Clinic de Neurologie si Psihiatrie Oradea
  • Spitalul Clinic Municipal "Dr.Gavril Curteanu" Oradea
  • Spitalul de Psihiatrie "Dr. Gh. Preda"
  • Spitalul Judetean de Urgenta Targoviste Clinica Psihiatrie Adulti nr. 7
  • Spitalul Clinic Judetean Mures, Clinica Psihiatrie Nr. 2

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CYP-1020

Risperidone

Arm Description

Dose titration 15-35mg/day for 6 months

Dose titration 2-6mg/day for 6 months

Outcomes

Primary Outcome Measures

Cognition
To evaluate the cognitive benefits of treatment with CYP-1020 (formerly known as BL-1020) compared to risperidone after 6 weeks of treatment in patients experiencing acute exacerbation of schizophrenia. Assessed by calculating difference between CYP-1020 and Risperidone on mean change from baseline to Week 6 endpoint on MATRICS Consensus Cognition Battery (MCCB) normative composite score. MCCB is a neuropsychological test battery that comprises 10 measures of 7 different cognitive areas including speed of processing, verbal learning, memory-verbal and non verbal reasoning and problem solving, visual learning, social cognition, attention/vigilance.The study was terminated after the interim analysis. MCBB total score ranges from -50 to 150. Change from Baseline by Visit (LOCF)Higher score means better cognitive functioning.

Secondary Outcome Measures

Long Term Cognition
Evaluation of the cognitive benefits of treatment with BL-1020 compared to risperidone after 12 and 24 weeks of treatment
Long Term Schizophrenia Treatment
Evaluation of the antipsychotic efficacy of BL-1020 compared to risperidone after 6, 12 and 24 weeks of treatment

Full Information

First Posted
May 30, 2011
Last Updated
September 17, 2014
Sponsor
BioLineRx, Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT01363349
Brief Title
Phase IIb-III Study of BL-1020 Small Molecule for Schizophrenia
Acronym
CLARITY
Official Title
A Randomized, Double-Blind, Active-Controlled,Phase 2/3 Study to Determine the Short-Term (6-Week) and Long-Term (6 Month) Cognitive and Anti-Psychotic Efficacy, Safety and Tolerability of CYP-1020 Compared to Risperidone in Patients With Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Terminated
Why Stopped
pre-planned interim analysis of the Phase II/III CLARITY trial of BL-1020 indicate that the trial would not meet the pre-specified primary efficacy endpoint.
Study Start Date
May 2011 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
April 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
BioLineRx, Ltd.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a randomized, double-blind, active-controlled, 6 month study designed to evaluate the cognitive effects of treatment with CYP-1020 compared to risperidone. The primary efficacy endpoint will occur after 6 weeks of treatment; additional (secondary) efficacy endpoints will occur after 12 and 24 weeks of treatment. Up to 450 patients will be randomized to CYP-1020 or risperidone in a 1:1 ratio. The study will utilize a flexible dose escalation scheme designed to allow patients to titrate to their maximally tolerated dose; doses of CYP-1020 may range from a minimum of 15 mg to a maximum of 35 mg, whereas doses of risperidone will range from a minimum of 1 mg to 3 mg BID (2-6 mg daily). To ensure effective blinding across all treatment groups, all patients will be treated twice daily with study drug and/or placebo, as indicated (i.e., double-dummy design).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Cognitive Effect on Schizophrenic Patients

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
269 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CYP-1020
Arm Type
Experimental
Arm Description
Dose titration 15-35mg/day for 6 months
Arm Title
Risperidone
Arm Type
Active Comparator
Arm Description
Dose titration 2-6mg/day for 6 months
Intervention Type
Drug
Intervention Name(s)
CYP-1020
Other Intervention Name(s)
BL-1020
Intervention Description
CYP-1020 (formerly known as BL-1020) is an orally available new chemical entity.
Intervention Type
Drug
Intervention Name(s)
Risperidone
Primary Outcome Measure Information:
Title
Cognition
Description
To evaluate the cognitive benefits of treatment with CYP-1020 (formerly known as BL-1020) compared to risperidone after 6 weeks of treatment in patients experiencing acute exacerbation of schizophrenia. Assessed by calculating difference between CYP-1020 and Risperidone on mean change from baseline to Week 6 endpoint on MATRICS Consensus Cognition Battery (MCCB) normative composite score. MCCB is a neuropsychological test battery that comprises 10 measures of 7 different cognitive areas including speed of processing, verbal learning, memory-verbal and non verbal reasoning and problem solving, visual learning, social cognition, attention/vigilance.The study was terminated after the interim analysis. MCBB total score ranges from -50 to 150. Change from Baseline by Visit (LOCF)Higher score means better cognitive functioning.
Time Frame
Baseline and 6 weeks
Secondary Outcome Measure Information:
Title
Long Term Cognition
Description
Evaluation of the cognitive benefits of treatment with BL-1020 compared to risperidone after 12 and 24 weeks of treatment
Time Frame
12 and 24 weeks of treatment
Title
Long Term Schizophrenia Treatment
Description
Evaluation of the antipsychotic efficacy of BL-1020 compared to risperidone after 6, 12 and 24 weeks of treatment
Time Frame
Baseline and 6, 12 and 24 weeks of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or non-pregnant or lactating female, 18-50 years of age inclusive Patients must have exhibited symptoms meeting the criteria of schizophrenia for at least one year, but not more than 20 years, prior to Screening Recent onset (not more than 30 days) of worsening of psychiatric symptoms at Screening. Currently experiencing an acute exacerbation of schizophrenia, as defined by the following results at Screening and Baseline: ≥70 total score on the PANSS ≥4 (moderate) on two of the following four PANSS items: (1) delusions, (2) hallucinatory behaviors, (3) conceptual disorganization or (4) suspiciousness/persecution, where at least one of the two items must be either delusions or hallucinatory behaviors CGI-S score between 4 and 6 (moderately ill to severely ill) at the Screening and Baseline visits. Has exhibited a sufficient clinical response to at least one previous course of an anti-psychotic agent prescribed at a generally recognized therapeutic dose. Must have completed at least 5 years of formal education or its equivalent Exclusion Criteria: Breastfeeding or pregnant Symptoms of schizophrenia for more than 20 years at the time of screening. Psychotic symptoms that have failed to improve (based on Investigator's opinion or documented medical history) following sufficient treatment with therapeutic doses of two or more anti-psychotics agents over the preceding 2 years Prior history of neuroleptic malignant syndrome Prior history or current evidence of moderate or severe tardive dyskinesia (mild is acceptable). Abnormal ECG evaluation History of confirmed epilepsy or prior seizure disorder (history of a single febrile seizure is not exclusionary) In the opinion of the investigator, unstable medical disease (e.g., malignancy, poorly controlled diabetes or hypertension, ischemic cardiac disease, dilated cardiomyopathy or valvular heart disease, pulmonary disease, liver disease, kidney disease) Acute infectious disease (e.g., malaria, dengue fever, hepatitis A), or chronic infectious disease (e.g., history of AIDS or HIV positivity, tuberculosis) Likely allergy, sensitivity or intolerance to BL-1020, perphenazine, risperidone, paliperidone, or any of the drug product excipients Any suicide attempt within the preceding 2 years Any Substance Dependence disorder High likelihood of substance abuse Diagnosis with one of the following DSM-IV-TR Axis I diagnoses: schizophreniform disorder, schizoaffective disorder, bipolar disorder, substance dependency, mood disorder with psychotic features; psychotic disorder NOS Requiring chronic treatment with benzodiazepines Requiring chronic treatment with mood stabilizers Previously treated with clozapine within 6 months prior to screening Any abnormal clinical laboratory test result that is judged by the Investigator to be clinically significant History of, or serologic evidence of, acute or chronic active hepatitis B or C
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arnon Aharon, MD
Organizational Affiliation
BioLineRx, Ltd.
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Psychiatry, Sheath VS General Hospital, Sheath KM School of Post Graduate Medicine & Research
City
Ahmedabad
Country
India
Facility Name
Saoji Tupkari Hospital
City
Aurangabad
Country
India
Facility Name
Spandana Nursing Home
City
Bangalore
Country
India
Facility Name
KHM Hospital
City
Chennai
Country
India
Facility Name
Asha Hospital
City
Hyderabad
Country
India
Facility Name
Department of Psychiatry, Owaisi Hospital & Research Centre
City
Hyderabad
Country
India
Facility Name
RK Yadav Memorial Mental Health and De-addiction Hospital
City
Jaipur
Country
India
Facility Name
Mahendru Psychiatric Centre
City
Kanpur
Country
India
Facility Name
Dreamland Nursing Home
City
Kolkata
Country
India
Facility Name
Dayanand Medical College & Hospital
City
Ludhiana
Country
India
Facility Name
Centre for Psychiatric Research, Department of Psychiatry, K.S Hegde Medical Academy
City
Mangalore
Country
India
Facility Name
Jaslok Hospital&Research Centre
City
Mumbai
Country
India
Facility Name
JSS Medical College Hospital
City
Mysore
Country
India
Facility Name
Sujata Birla Hospital
City
Nashik
Country
India
Facility Name
Vimhans Hospital
City
New Delhi
Country
India
Facility Name
S.V.Medical College
City
Tirupati
Country
India
Facility Name
Deva Mental Health Care
City
Varanasi
Country
India
Facility Name
Vijayawada Institute of Mental Health & Neurosciences
City
Vijayawada
Country
India
Facility Name
IMSP Spitalul Clinic de Psihiatrie, Sectia 14
City
Chisinau
Country
Moldova, Republic of
Facility Name
IMSP Spitalul Clinic de Psihiatrie, Sectia 17
City
Chisinau
Country
Moldova, Republic of
Facility Name
IMSP Spitalul Clinic de Psihiatrie, Sectia 8
City
Chisinau
Country
Moldova, Republic of
Facility Name
pitalul Clinic Judetean de Urgenta Arad Clinica Psihiatrie
City
Arad
Country
Romania
Facility Name
Spitalul de Psihiatrie si Neurologie Brasov
City
Brasov
Country
Romania
Facility Name
Spitalul Clinic de Psihiatrie "Prof. Dr. Al. Obregia"
City
Bucharest
Country
Romania
Facility Name
Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 13
City
Bucharest
Country
Romania
Facility Name
Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 1
City
Bucharest
Country
Romania
Facility Name
Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 8
City
Bucharest
Country
Romania
Facility Name
Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 9
City
Bucharest
Country
Romania
Facility Name
Spitalul de Psihiatrie C.E.T.T.T. "Sf. Stelian"
City
Bucharest
Country
Romania
Facility Name
Spitalul Judetean Cluj Napoca
City
Cluj Napoca
Country
Romania
Facility Name
Spitalul Clinic Judetean de Urgenta Constanţa Clinica de Psihiatrie
City
Constanta
Country
Romania
Facility Name
Spitalul Clinic de Neuropsihiatrie Clinica de Psihiatrie nr. 2
City
Craiova
Country
Romania
Facility Name
Spitalul de Neuropsihiatrie Clinica de Psihiatrie I
City
Craiova
Country
Romania
Facility Name
Spitalul Clinic de Psihiatrie Socola
City
Iasi
Country
Romania
Facility Name
Spital Clinic de Neurologie si Psihiatrie Oradea
City
Oradea
Country
Romania
Facility Name
Spitalul Clinic Municipal "Dr.Gavril Curteanu" Oradea
City
Oradea
Country
Romania
Facility Name
Spitalul de Psihiatrie "Dr. Gh. Preda"
City
Sibiu
Country
Romania
Facility Name
Spitalul Judetean de Urgenta Targoviste Clinica Psihiatrie Adulti nr. 7
City
Targoviste
Country
Romania
Facility Name
Spitalul Clinic Judetean Mures, Clinica Psihiatrie Nr. 2
City
Targu-Mures
Country
Romania

12. IPD Sharing Statement

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Phase IIb-III Study of BL-1020 Small Molecule for Schizophrenia

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