Safety, Tolerability, and Pharmacokinetic Study of Single Ascending Doses of GC021109 in Healthy Subjects

Healthy Volunteers Clinical Trial

Official title:

A Randomized, Phase 1, Double-Blind, Placebo-Controlled, First-in-Human, Safety, Tolerability, and Pharmacokinetic Study of Single Ascending Doses of GC021109 in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02254369
• Other study ID #: GC-100-01
• Status: Completed
• Phase: Phase 1
• First received: September 29, 2014
• Last updated: February 17, 2015
• Start date: September 2014
• Est. completion date: December 2014

Study information

• Verified date: February 2015
• Source: GliaCure, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary objective of the study is to assess the safety and tolerability of single oral doses of GC021109 when administered to healthy adult subjects.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: December 2014
• Est. primary completion date: December 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Healthy adult male and/or non-childbearing potential females, 18 to 55 years of age, inclusive, at the time of informed consent.

2. Continuous non-smoker who has not used nicotine-containing products for at least 3 months prior to dosing of study drug.

3. BMI = 18.5 and = 32.0 (kg/m2) at screening with a maximum weight of 120 kg.

4. Medically healthy with no clinically significant screening results that would exclude subject from the study as deemed by the PI.

5. Females must have undergone 1 of the following sterilization procedures, and have official documentation, at least 6 months prior to dosing of study drug:

• Hysteroscopic sterilization

• Bilateral tubal ligation or bilateral salpingectomy

• Hysterectomy.

• Bilateral oophorectomy. OR be postmenopausal with amenorrhea for at least 1 year prior to dosing of study drug and have follicle-stimulating hormone (FSH) serum levels consistent with postmenopausal status.

6. All male subjects must agree to use a condom with spermicide or abstain from sexual intercourse during the study until 90 days beyond the last dose of study drug.

7. If male, must agree to not donate sperm from Day -1 until 90 days after dosing.

8. Understand the study procedures in the ICF, and be willing and able to comply with the protocol.

Exclusion Criteria:

1. Subject is mentally or legally incapacitated or has significant emotional problems at the time of screening visit or expected during the conduct of the study.

2. History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the PI.

3. History of any illness that, in the opinion of the PI, might confound the results of the study or pose an additional risk to the subject by their participation in the study.

4. History or presence of alcoholism or drug abuse within the past 2 years prior to screening.

5. History or presence of hypersensitivity or idiosyncratic reaction to component of the study drug or related compounds.

6. History of cancer within the past 5 years (excluding non-melanoma skin cancer) prior to screening.

7. Clinically significant abnormal screening laboratory test values (as determined by the

PI), including, but not limited to, the following:

• any values for alanine aminotransferase (ALT) or aspartate aminotransferase (AST) that are above the upper limit of the reference range at screening or check-in.

• any values for total or direct bilirubin that are 1.5 times above the upper limit of the reference range at screening or check-in.

• estimated creatinine clearance <90 mL/min at screening only.

8. Clinically significant infection within 3 months prior to screening as determined by the PI.

9. Female subjects of child-bearing potential.

10. Female subjects who are pregnant or lactating.

11. Positive urine drug or urine alcohol results at screening or check-in.

12. Positive urine cotinine at screening.

13. Positive results at screening for HIV, hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV).

14. Seated blood pressure is less than 90/40 mmHg or greater than 140/90 mmHg at screening.

15. Seated heart rate is lower than 40 bpm or higher than 99 bpm at screening.

16. Orthostatic vital sign results as deemed clinically significant in the opinion of the PI at screening.

17. QTcB interval is >430 msec (males) or >450 msec (females) or deemed clinically abnormal by the PI, prior to dosing of study drug.

18. Unable to refrain from or anticipates the use of:

• Any drug, including prescription and non-prescription medications, herbal remedies, vitamin supplements or substrates of CYP1A2, CYP3B6, or CYP3A4 beginning 14 days prior to dosing of study drug and throughout the study. Acetaminophen (up to 2 g per 24 hour period) may be permitted during the study.

• Any drugs known to be significant inducers of CYP enzymes and/or P-glycoprotein (P-gp), including St. John's Wort, for 28 days prior to dosing of study drug and throughout the study. Appropriate sources will be consulted by the PI or designee to confirm lack of PK/PD interaction with study drug.

19. Has been on a diet incompatible with the on-study diet, in the opinion of the PI, within the 28 days prior to dosing of study drug, and throughout the study.

20. Has donated blood within 3 months of screening visit or plans to donate blood within 3 months of study completion, except for blood collected during another clinical trial performed 30 days prior to screening.

21. Plasma donation within 7 days prior to dosing of study drug.

22. Participation in another clinical trial within 30 days prior to screening. The 30-day window will be derived from the date of the last study scheduled blood collection or dosing, whichever is later, in the previous study to the date of screening for the current study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Healthy Volunteers

Intervention

Drug:
• GC021109

Other:
• Placebo

Locations

Country	Name	City	State
United States	Celerion	Neptune	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
GliaCure, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number and severity of TEAEs		following single dosage	Yes