Schizophrenia
Conditions
Keywords
Schizophrenia
Brief summary
This is a single-site, randomized, double-blind, placebo-controlled, multiple dose, flexible dosage range, PK and PD study of SKL15508 as monotherapy in subjects with stable schizophrenia.
Interventions
DRUGSKL15508
DRUGPlacebo
Sponsors
SK Life Science, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No
Inclusion criteria
1. The subject or, when applicable, the subject's legally acceptable representative signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any study procedures. 2. Participants who are nonsterile and sexually active agree to use a double-barrier method of contraception (must be used regardless of any other contraception in use) from the time of providing informed consent throughout the duration of the study and for 12 weeks after the last dose of study drug. Nonsterile males must be advised not to donate sperm and women should not donate ova throughout the duration of the study and for 12 weeks after the last dose of study drug. 3. Must be male or non-pregnant, non-lactating female subjects, 18 to 60 years of age, inclusive 4. Has a body mass index (BMI) between 18.0 and 38.0 kg/m2, inclusive 5. Has a clinical diagnosis of schizophrenia and, in the opinion of the Investigator, is able to safely be off his or her prescribed antipsychotic medications while participating in the study and has a very high likelihood of not deteriorating over a 3-week timeframe when off standard of care as outpatients during the Screening Period 6. Has been receiving a stable dose of antipsychotic medication for at least 1 month before Screening 7. Has not had an acute exacerbation of psychosis or hospitalization for the treatment of schizophrenia for at least 3 months before Screening 8. By history, has not had a marked change in smoking or tobacco/nicotine use from 30 days before Screening. 9. Must reside in a stable residence for at least 8 weeks before the Screening Visit
Exclusion criteria
1. At risk of suicide (e.g., per Columbia Suicide Severity Rating Scale \[C-SSRS\]) or have made a suicide attempt in the 6 months before Screening 2. Has a known sensitivity to sulfur-containing drugs or sulfates in food 3. Taking any medication known to influence coagulation, such as acetylsalicylic acid (aspirin), and including prescription, herbal remedies, vitamin supplements and over-the-counter products 4. Has uncontrolled, clinically significant neurologic, cardiovascular, pulmonary, hepatic, renal, metabolic, gastrointestinal or endocrine disease or other abnormality (other than the disease being studied), which may impact the ability of the subject to participate or potentially confound the study results 5. Has a positive urine drug result for drugs of abuse (i.e., illicit, illegal or without valid prescription or medical need) at Screening or Admission 6. Has donated or lost 450 mL or more of his or her blood volume (including plasmapheresis), or had a transfusion of any blood product within 45 days before Day 1 7. Has an abnormal (clinically significant) electrocardiogram (ECG) at Screening or unit admission day 8. Has a blood pressure and pulse rate outside the protocol defined ranges 9. Has a QT interval or PR outside of the protocol defined ranges 10. Has abnormal laboratory values that suggest a clinically significant underlying disease 11. Has a history of a primary DSM-IV axis I diagnosis other than schizophrenia 12. Has a medical condition other than schizophrenia (e.g., dementia, antisocial personality, borderline personality disorders) that can cause cognitive impairment or interfere with the performance or completion of study-defined procedures 13. Has been taking medication for a medical condition for less than 2 months even if at a stable dose or regimen 14. Currently taking lithium or any psychotropic medication that cannot be discontinued for safety reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number and percent of subjects experiencing an adverse event. | 10 days |
| Change from baseline in event-related potentials (ERP) following multiple oral doses of SKL15508. | During the course of 10 days |
| Change from baseline in clinical laboratory assessments. | 10 days |
| Change from baseline in vital signs. | 10 days |
Countries
United States
Outcome results
None listed