A Study to Evaluate the Safety, Tolerance, and Pharmacokinetic and Pharmacodynamic Profile Of 1 SR Formulation of EB-1020

Phase 1

Completed

• Conditions: Normal, Healthy Volunteers
• Interventions: Drug: EB-1020 IR; Other: Placebo; Drug: EB-1020 SR1; Drug: EB-1020 SR2; Drug: EB-1020 SR3

• Registration Number: NCT01744808
• Lead Sponsor: Neurovance, Inc.

Brief Summary

To investigate whether there is a food-effect with oral administration with EB-1020 as well as to obtain information on the safety, and tolerability of EB-1020 in a range of doses.

Detailed Description

* To investigate the safety and tolerance of single doses of EB-1020 immediate release (IR) versus three sustained release (SR) formulations.

* To investigate the safety and tolerance of a single oral dose of a SR formulation of EB-1020 in the fed and fasted state.

* To investigate the safety, tolerance, and cognitive effects of multiple oral rising doses of a SR formulation of EB-1020.

Secondary Objectives

* To characterize the single dose and steady state pharmacokinetic profiles of EB-1020 SR formulations.

* To investigate the effect of food on the pharmacokinetic profile of EB-1020 SR following single oral doses.

Study Timeline

• Study First Submitted: 2012-11-19
• Study First Submitted QC: 2012-12-05
• Study First Posted: 2012-12-07
• Study Start: 2013-02
• Primary Completion: 2014-02
• Study Completion: 2014-02
• Status Verified: 2014-04
• Last Update Submitted: 2014-04-02
• Last Update Posted: 2014-04-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 54

Inclusion Criteria

1. Aged 18-45 years inclusive
2. Body weight with the normal range for height (body mass index [BMI] between 19-30 kg/m2 inclusive)
3. If female, be of non-child bearing potential (surgically sterile, post-menopausal for 12 months or receiving a stable dose of implanted or injectable contraceptive for at least 3 months with last dose of injectable contraceptive within 2 months). Non-surgical menopause history must be confirmed by follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels as defined by established lab ranges.
4. Be in general good health without clinically significant medical history
5. Have clinical laboratory test results that are within the laboratory reference range; or if out of range are not clinically relevant and are acceptable to the Investigator and Sponsor medical representative
6. Negative Human Immunodeficiency Virus (HIV), Hepatitis B and Hepatitis Screening test
7. Able and willing to give written informed consent

Exclusion Criteria

1. Receipt of any investigational agent or drug within 3 months of entry into the study
2. Use of prescription drugs within 4 weeks prior to first dosing. Subjects who have used over the counter medication excluding paracetamol, topical over the counter medications and routine vitamins but including megadose (intake of 20 to 600 times the recommended daily dose) vitamin therapy within 7 days of first dosing, unless agreed as non-clinically relevant by the Principal Investigator and Sponsor
3. A history of, or current evidence for, suicidal ideation, based upon clinical interview and a psychiatric questionnaire
4. A history of known or suspected seizures, spasms, infantile spasms, febrile convulsions, unexplained significant and recent loss of consciousness or history of significant head trauma with loss of consciousness or a family history (first degree relative) of epilepsy or seizures (fits)
5. A history of sleep problems in the last 3 months
6. A history of relevant atopy or drug hypersensitivity
7. A history (within the last 5 years) or evidence of alcohol or drug abuse. Subject who consume more than 14 units (female) or 21 (male) units of alcohol a week (unit = 1 glass (125 mL) of wine = 1 measure of spirits = ½ pint of beer) will also be ineligible
8. A positive urine test for drugs of abuse or alcohol at Screening or on the day of admittance to the Study Unit
9. A history of smoking in the last 3 months
10. Have a significant infection (such as influenza) or known inflammatory process on screening or admission
11. Have acute gastrointestinal symptoms at the time of screening or admission (e.g. nausea, vomiting, diarrhea, heartburn )
12. Have previously received EB-1020
13. Be vegetarians, vegans or have medical dietary restrictions
14. Any major surgical procedure within one month of entry into the study
15. Have difficulties communicating reliably with the Investigator or appear unlikely to co-operate with the requirements of the study in the investigator's judgment.
16. Any other condition which in the view of the Investigator is likely to interfere with study or put the subject at risk.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
EB-1020 IR	EB-1020 IR	Immediate Release Formulation
Placebo	Placebo	Placebo Formulation
EB-1020 SR1	EB-1020 SR1	Sustained release formulation
EB-1020 SR2	EB-1020 SR2	Sustained Release Formulation
EB-1020 SR3	EB-1020 SR3	Sustained Release Formulation

Primary Outcome Measures

Name	Time	Method
Cmax	up to 6 months	Pharmacokinetic parameters
Tmax	up to 6 months	Pharmacokinetic parameter
AUC	up to 6 months	Pharmacokinetic parameter

Secondary Outcome Measures

Name	Time	Method
Effect of food on Cmax	up to 6 months

Trial Locations

Locations (1)

Nucleus Network Ltd.; 🇦🇺 Melbourne, Victoria, Australia