Trials / Completed
CompletedNCT00480571
Safety and Tolerability of BL-1020 in Hospitalized Subjects With Chronic Schizophrenia or Schizo-Affective Disorder
An Open-label, Multi-center, 6-week, Sequential Cohort Study Designed to Determine the Safety and Tolerability of Two Dose Ranges of BL-1020 in Hospitalized Subjects With Chronic Schizophrenia or Schizo-affective Disorder
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- Sponsor
- BioLineRx, Ltd. · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
An open-label, multi-center, 6-week, sequential cohort study designed to determine the safety and tolerability of two dose ranges of BL-1020 in hospitalized subjects with chronic schizophrenia or schizo-affective disorder
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | BL-1020 | BL-1020 Low Dose |
| DRUG | BL 1020 High Dose | BL 1020 High Dose |
Timeline
- Start date
- 2007-06-01
- Primary completion
- 2007-12-01
- Completion
- 2007-12-01
- First posted
- 2007-05-31
- Last updated
- 2009-07-21
Locations
2 sites across 2 countries: Israel, Romania
Source: ClinicalTrials.gov record NCT00480571. Inclusion in this directory is not an endorsement.