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

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ClinicalTrials.gov Identifier: NCT02254369
Recruitment Status : Completed
First Posted : October 1, 2014
Last Update Posted : February 18, 2015
Sponsor:
Information provided by (Responsible Party):
GliaCure, Inc.

Brief 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.

Condition or disease Intervention/treatment Phase
Healthy Volunteers Drug: GC021109 Other: Placebo Phase 1

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 44 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
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
Study Start Date : September 2014
Actual Primary Completion Date : December 2014
Actual Study Completion Date : December 2014

Arm Intervention/treatment
Experimental: Cohort 1- GC021109
single dose, 0.0014 mg/kg GC021109
Drug: GC021109
Experimental: Cohort 2- GC021109
single dose, 0.014 mg/kg GC021109
Drug: GC021109
Experimental: Cohort 3-GC021109
single dose, 0.14 mg/kg GC021109
Drug: GC021109
Experimental: Cohort 4- GC021109
single dose, 1.4 mg/kg GC021109 subjects will receive GC021109 under fasting then under fed conditions separated by a washout of 14 (± 1) days after the first dose.
Drug: GC021109
Experimental: Cohort 5- GC021109
single dose, 4.2 mg/kg GC021109
Drug: GC021109
Placebo Comparator: Cohort 1- placebo
single dose, 0.0014 mg/kg matching placebo
Other: Placebo
Placebo Comparator: Cohort 2- placebo
single dose, 0.014 mg/kg matching placebo
Other: Placebo
Placebo Comparator: Cohort 3- placebo
single dose, 0.14 mg/kg matching placebo
Other: Placebo
Placebo Comparator: Cohort 4- placebo
single dose, 1.4 mg/kg subjects will receive matching placebo under fasting then under fed conditions separated by a washout of 14 (+/- 1) days after the first dose.
Other: Placebo
Placebo Comparator: Cohort 5- placebo
single dose, 4.2 mg/kg matching placebo
Other: Placebo



Primary Outcome Measures :
  1. Number and severity of TEAEs [ Time Frame: following single dosage ]


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Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02254369


Locations
United States, New Jersey
Celerion
Neptune, New Jersey, United States, 07753
Sponsors and Collaborators
GliaCure, Inc.

Responsible Party: GliaCure, Inc.
ClinicalTrials.gov Identifier: NCT02254369     History of Changes
Other Study ID Numbers: GC-100-01
First Posted: October 1, 2014    Key Record Dates
Last Update Posted: February 18, 2015
Last Verified: February 2015