Status:
COMPLETED
Safety and Tolerability Comparison of Immediate and Controlled Release Formulations of Ecopipam
Lead Sponsor:
Emalex Biosciences Inc.
Collaborating Sponsors:
Psyadon Pharma
Conditions:
Healthy
Eligibility:
MALE
18-45 years
Phase:
PHASE1
Brief Summary
Ecopipam hydrochloride (HCl) is an investigational drug being studied for several possible diseases. To date, all clinical studies have been done using the ecopipam immediate release (IR) tablet. Howe...
Detailed Description
Ecopipam hydrochloride (HCl) is an investigational drug being studied for several possible diseases. To date, all clinical studies have been done using the ecopipam immediate release (IR) tablet. Howe...
Eligibility Criteria
Inclusion
- Signed and dated, IRB-approved informed consent form before any protocol-specific screening procedures
- Non-smoking male subjects between the ages of 18 and 45 years (inclusive)
- In good general health as determined by a thorough medical history and physical examination, ECG, vital signs, and clinical laboratory evaluation
- Willing and able to complete all study assessments and procedures
- Body mass index (BMI) between 18 and 30 kg/m2 (inclusive) and a weight between 65 and 100 kg (inclusive)
- QTcB interval (Bazett's correction factor) of the baseline ECG must be ≤ 450 ms at screening
Exclusion
- Subjects with a history of suicide attempt or with past or current active suicidal ideation
- Subjects with a history of seizures or with head trauma leading to loss of consciousness
- Subjects with clinically significant neurologic, cardiovascular, hepatic, renal, endocrinologic, pulmonary, hematological, psychiatric, or other medical illness that would interfere with participation in this study
- History of any primary malignancy, with the exception of basal cell or squamous cell carcinomas of the skin or cervical carcinoma in situ or other malignancies curatively treated and with no evidence of disease for at least 5 years
- Supine blood pressure \>140/90 mm/Hg or resting heart rate ≥100 bpm at the screening visit
- History of substance-related disorders (with the exception of caffeine-related and nicotine-related disorders) or eating disorders as defined in the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) within 1 year of screening
- History of smoking or the use of nicotine containing products within 3 months of screening by self reporting
- A positive alcohol Breathalyzer or urine drug screen for drugs of abuse at the screening visit or at the beginning of the inpatient period
- Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to the beginning of the screening period
- Treatment with any other prescription or non-prescription drugs (including vitamins, herbal, and dietary supplements) within 7 days or 5 half-lives of the screening visit, whichever is longer. Acetaminophen will be permitted for intermittent treatment at doses of less than 2 grams/day
- Subjects with a history of previous administration of ecopipam or of an allergic reaction or hypersensitivity to any drug or to any component of the CR formulation
- Blood collection or blood loss of greater than 500 mL within 56 days prior to screening
- Positive for human immunodeficiency virus (HIV) at screening
- Positive for Hepatitis B surface antigen (HbsAg) or positive Hepatitis C virus (HCV) antibody at screening
- Any other condition and/or situation that causes the investigator to deem a subject unsuitable for the study (e.g., due to expected study medication non-compliance, inability to medically tolerate the study procedures, or a subject's unwillingness to comply with study-related procedures)
Key Trial Info
Start Date :
August 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2012
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT01408394
Start Date
August 1 2011
End Date
May 1 2012
Last Update
April 19 2024
Active Locations (1)
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1
SNBL Clinical Pharmacology Center, Inc.
Baltimore, Maryland, United States, 21201