Phase IIb-III Study of BL-1020 Small Molecule for Schizophrenia (CLARITY)
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Purpose
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).
| Condition | Intervention | Phase |
|---|---|---|
|
Schizophrenia Cognitive Effect on Schizophrenic Patients |
Drug: CYP-1020 Drug: Risperidone |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| 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 |
- Cognition [ Time Frame: Baseline and 6 weeks ] [ Designated as safety issue: No ]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 exacerbations of schizophrenia
- Long term cognition [ Time Frame: 12 and 24 weeks of treatment ] [ Designated as safety issue: No ]Evaluation of the cognitive benefits of treatment with BL-1020 compared to risperidone after 12 and 24 weeks of treatment
- Long term schizophrenia treatment [ Time Frame: Baseline and 6, 12 and 24 weeks of treatment ] [ Designated as safety issue: No ]Evaluation of the antipsychotic efficacy of BL-1020 compared to risperidone after 6, 12 and 24 weeks of treatment
| Estimated Enrollment: | 435 |
| Study Start Date: | May 2011 |
| Arms | Assigned Interventions |
|---|---|
| Experimental: CYP-1020 |
Drug: CYP-1020
CYP-1020 (formerly known as BL-1020) is an orally available new chemical entity.
Other Name: BL-1020
|
|
Active Comparator: Risperidone
2-6 mg, 6 months
|
Drug: Risperidone |
Eligibility| Ages Eligible for Study: | 18 Years to 50 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
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
Contacts and Locations| India | |
| Department of Psychiatry, Sheath VS General Hospital, Sheath KM School of Post Graduate Medicine & Research | |
| Ahmedabad, India | |
| Saoji Tupkari Hospital | |
| Aurangabad, India | |
| Spandana Nursing Home | |
| Bangalore, India | |
| KHM Hospital | |
| Chennai, India | |
| Department of Psychiatry, Owaisi Hospital & Research Centre | |
| Hyderabad, India | |
| Asha Hospital | |
| Hyderabad, India | |
| RK Yadav Memorial Mental Health and De-addiction Hospital | |
| Jaipur, India | |
| Mahendru Psychiatric Centre | |
| Kanpur, India | |
| Dreamland Nursing Home | |
| Kolkata, India | |
| Dayanand Medical College & Hospital | |
| Ludhiana, India | |
| Centre for Psychiatric Research, Department of Psychiatry, K.S Hegde Medical Academy | |
| Mangalore, India | |
| Jaslok Hospital&Research Centre | |
| Mumbai, India | |
| JSS Medical College Hospital | |
| Mysore, India | |
| Sujata Birla Hospital | |
| Nashik, India | |
| Vimhans Hospital | |
| New Delhi, India | |
| S.V.Medical College | |
| Tirupati, India | |
| Deva Mental Health Care | |
| Varanasi, India | |
| Vijayawada Institute of Mental Health & Neurosciences | |
| Vijayawada, India | |
| Moldova, Republic of | |
| IMSP Spitalul Clinic de Psihiatrie, Sectia 14 | |
| Chisinau, Moldova, Republic of | |
| IMSP Spitalul Clinic de Psihiatrie, Sectia 8 | |
| Chisinau, Moldova, Republic of | |
| IMSP Spitalul Clinic de Psihiatrie, Sectia 17 | |
| Chisinau, Moldova, Republic of | |
| Romania | |
| pitalul Clinic Judetean de Urgenta Arad Clinica Psihiatrie | |
| Arad, Romania | |
| Spitalul de Psihiatrie si Neurologie Brasov | |
| Brasov, Romania | |
| Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 8 | |
| Bucharest, Romania | |
| Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 13 | |
| Bucharest, Romania | |
| Spitalul Clinic de Psihiatrie "Prof. Dr. Al. Obregia" | |
| Bucharest, Romania | |
| Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 9 | |
| Bucharest, Romania | |
| Spitalul Clinic de Psihiatrie Dr. Alexandru Obregia Department 1 | |
| Bucharest, Romania | |
| Spitalul de Psihiatrie C.E.T.T.T. "Sf. Stelian" | |
| Bucharest, Romania | |
| Spitalul Judetean Cluj Napoca | |
| Cluj Napoca, Romania | |
| Spitalul Clinic Judetean de Urgenta Constanţa Clinica de Psihiatrie | |
| Constanta, Romania | |
| Spitalul Clinic de Neuropsihiatrie Clinica de Psihiatrie nr. 2 | |
| Craiova, Romania | |
| Spitalul de Neuropsihiatrie Clinica de Psihiatrie I | |
| Craiova, Romania | |
| Spitalul Clinic de Psihiatrie Socola | |
| Iasi, Romania | |
| Spital Clinic de Neurologie si Psihiatrie Oradea | |
| Oradea, Romania | |
| Spitalul Clinic Municipal "Dr.Gavril Curteanu" Oradea | |
| Oradea, Romania | |
| Spitalul de Psihiatrie "Dr. Gh. Preda" | |
| Sibiu, Romania | |
| Spitalul Judetean de Urgenta Targoviste Clinica Psihiatrie Adulti nr. 7 | |
| Targoviste, Romania | |
| Spitalul Clinic Judetean Mures, Clinica Psihiatrie Nr. 2 | |
| Targu-Mures, Romania | |
More Information
No publications provided
| Responsible Party: | BioLineRx, Ltd. |
| ClinicalTrials.gov Identifier: | NCT01363349 History of Changes |
| Obsolete Identifiers: | NCT01365299 |
| Other Study ID Numbers: | 1020-CLIN-201 |
| Study First Received: | May 30, 2011 |
| Last Updated: | April 10, 2013 |
| Health Authority: | India: Drugs Controller General of India Romania: National Medicines Agency Moldavia: Ministry of Health |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders Risperidone Serotonin Antagonists Serotonin Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Pharmacologic Actions |
Physiological Effects of Drugs Antipsychotic Agents Tranquilizing Agents Central Nervous System Depressants Central Nervous System Agents Therapeutic Uses Psychotropic Drugs Dopamine Antagonists Dopamine Agents |
ClinicalTrials.gov processed this record on May 23, 2013