Single-Dose Pharmacokinetics (PK) Study of Novel Neurogenic Compound NSI-189

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Neuralstem Inc.
ClinicalTrials.gov Identifier:
NCT01310881
First received: February 24, 2011
Last updated: November 17, 2011
Last verified: May 2011
  Purpose

This is a subject single blinded, randomized, placebo-controlled, single dose, first-time-in-human study with three or more ascending cohorts.


Condition Intervention Phase
Depression
Drug: NSI-189 Phosphate
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Phase 1, Randomized, Subject Single Blinded, Placebo-Controlled, Single-Dose Escalation Study Evaluating the Safety, Tolerability, and Pharmacokinetics (PK) of NSI-189 Phosphate in Healthy Subjects

Resource links provided by NLM:


Further study details as provided by Neuralstem Inc.:

Primary Outcome Measures:
  • Safety of drug assessed by number and severity of adverse events in drug vs placebo groups [ Time Frame: 7 days ] [ Designated as safety issue: Yes ]
    Values for vital signs, standard physical examination, ECG, EEG and standard clinical laboratory tests (haematology and biochemistry), and for standard neurological exam and the Columbia Suicide Severity Rating Scale will be compared between NS189 and placebo.


Secondary Outcome Measures:
  • Pharmacokinetics of NS189 will be determined by plasma sample collection at various timepoints post-dosing, and measuring concentration of drug over time. [ Time Frame: 7 days ] [ Designated as safety issue: Yes ]
    Concentration of NS189 will be measured in plasma and standard PK values determined: AUC, Cmax, Tmax, T1/2, CL, Vz


Enrollment: 35
Study Start Date: February 2011
Study Completion Date: November 2011
Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Dose 1 Drug: NSI-189 Phosphate
Once daily oral administration
Experimental: Dose 2 Drug: NSI-189 Phosphate
Once daily oral administration
Experimental: Dose 3 Drug: NSI-189 Phosphate
Once daily oral administration
Experimental: Dose 4 Drug: NSI-189 Phosphate
Once daily oral administration
Experimental: Dose 5 Drug: NSI-189 Phosphate
Once daily oral administration
Experimental: Dose 6 Drug: NSI-189 Phosphate
Once daily oral administration
Experimental: Dose 7 Drug: NSI-189 Phosphate
Once daily oral administration

Detailed Description:

Each subject will undergo Screening (Day -28 to Day -2). Subjects will return to the clinical site on Day -1, be admitted to the unit, and eligibility will be reconfirmed. Eligible subjects will receive a single dose of investigational medicinal product (IMP, NSI-189 Phosphate or Placebo) on Day 1 and will be followed for safety and PK until discharge on Day 3. Subjects who are experiencing any significant AEs that are considered possibly related to study drug will be kept at the unit for an additional day (or longer) until the event resolves or it is considered medically safe for the subject to be discharged. Subjects will have a telephone Follow-up on Day 4 and return to the unit on Day 7 (± 1) for End-of-study. Participation of an individual subject may last up to 36 days from the time of Screening until the End-of-study.

  Eligibility

Ages Eligible for Study:   18 Years to 55 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • A subject must meet all of the following criteria:

    1. Subject has the ability to understand the purpose and risks of the study and to provide signed and dated informed consent.
    2. Males and females between 18 to 55 years of age, inclusive, at the time of informed consent.
    3. The following applies to female subjects:

      • Non-childbearing potential (surgically sterile [hysterectomy or bilateral tubal ligation] or post-menopausal ≥ 1 year with follicle stimulating hormone >40 U/L).

    4. The following applies to male subjects:

      • Male subjects with a female partner of childbearing potential will be required to use an effective method of birth control or practice abstinence during this study and for 3 months following discontinuation of IMP.

    5. Non-smokers (or other nicotine use) as determined by history (no nicotine use over the past year) and by negative urine cotinine test at screening and Day -1.
    6. BMI ≥ 19.5 and ≤30.0 kg/m2, at screening. Bodyweight must be >50 kg.
    7. Healthy, determined by pre-study medical evaluation and investigator discretion (medical history, physical examination, vital signs, ECG, and clinical laboratory evaluations).

Exclusion Criteria:

  1. Clinically significant history or evidence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, neurological, immunological, dermatological or psychiatric disorder(s), or other major disease as determined by the Investigator or designee.
  2. History of seizures including febrile seizures, loss of consciousness, or any clinically significant finding on the neurologic examination.
  3. Clinically significant abnormal clinical chemistry values, as determined by the Investigator.
  4. Clinically significant (as determined by the Investigator) 12-lead ECG abnormalities, including corrected QT interval using Bazett's correction method of >450 msec for males and >470 msec for females.
  5. History of severe allergic or anaphylactic reactions.
  6. Subjects who have plans to undergo elective procedures/surgeries at any time during the study through the follow-up visits.
  7. A positive screening test for human immunodeficiency virus (HIV), hepatitis C virus antibody (HCVAb), hepatitis B core antibody (HBcAb), or hepatitis B surface antigen (HBsAg).
  8. Serious infection (e.g. pneumonia, septicemia) as determined by the Investigator within 3 months prior to Day -1.
  9. Fever or bacterial, or viral infection (including upper respiratory tract infection) within 2 weeks prior to Day -1.
  10. Treatment with any prescribed medication within 28 days prior to Day -1.
  11. Treatment with any over-the-counter products (OTC), including herbal and/or alternative health preparations and procedures within the 14 days prior to Day -1. Note: Intermittent treatment with acetaminophen [≤1000 mg/day] and/or ibuprofen [≤400 mg/day] is permitted.
  12. Current enrollment in any other drug, biologic, device, or clinical study, or treatment with an investigational product or approved therapy for investigational use within 30 days (or 5 half-lives, whichever is longer) prior to Day -1.
  13. Any live or attenuated immunization/vaccination within 1 month prior to the study drug administration or planned to occur during the study period.
  14. Donation of blood (>500 mL) or blood products within 1 month prior to screening.
  15. History of alcohol or substance abuse (cocaine, amphetamines, barbiturates, opiates, benzodiazepines, cannabinoids, etc.) (as determined by the Investigator).
  16. Vigorous exercise (as determined by the Investigator) within 48 hours prior to the study drug administration.
  17. Inability to comply with study requirements.
  18. Any disorder that would interfere with the absorption, distribution, metabolism, or excretion of drugs.
  19. Any concurrent disease or condition that, in the opinion of the Investigator, would make the subject unsuitable for participation in the clinical study.
  20. Subject unwilling to avoid consumption of coffee and caffeine containing beverages within 48 hours prior to Day -1 until discharge from the clinical site.
  21. Use of an investigational product within 30 days prior to Day -1.
  22. Subject is unable to understand the protocol requirements, instructions and study-related restrictions, the nature, scope and possible consequences of the clinical study.
  23. Subject is unlikely to comply with the protocol requirements, instructions and study-related restrictions.
  24. Subject has previously been enrolled in this clinical study.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01310881

Locations
United States, California
California Clinical Trials
Glendale, California, United States, 91206
Sponsors and Collaborators
Neuralstem Inc.
Investigators
Study Director: Karl Johe, PhD Neuralstem Inc.
Principal Investigator: David Han, MD California Clinical Trials
  More Information

Publications:
Responsible Party: Neuralstem Inc.
ClinicalTrials.gov Identifier: NCT01310881     History of Changes
Other Study ID Numbers: NS2010-2
Study First Received: February 24, 2011
Last Updated: November 17, 2011
Health Authority: United States: Food and Drug Administration

Keywords provided by Neuralstem Inc.:
Neurogenesis
hippocampal stem cells
depression
stroke

Additional relevant MeSH terms:
Depression
Depressive Disorder
Behavioral Symptoms
Mood Disorders
Mental Disorders

ClinicalTrials.gov processed this record on April 17, 2014