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Safety and Pharmacokinetics Study of Healthy Male Adults When Repeatedly Administered Through Intravenous Injection

Primary Purpose

Hepatitis B

Status
Completed
Phase
Phase 1
Locations
Korea, Republic of
Study Type
Interventional
Intervention
GC1102
JW normal saline
Sponsored by
Green Cross Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hepatitis B

Eligibility Criteria

20 Years - 45 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Those who are healthy, male adult aged 20 years- 45 years when screened.
  • Those whose body weights are over 45kg when screened, and whose BMI scores are 19kg/㎡-28 kg/㎡.
  • Those whose HBs-Ag, HBc-Ab(IgM), HBc-Ab(IgG), HBV DNA quantitative are all negative when screened.
  • Those whose HBs-Ab(titer) in blood is below 500 IU/L when screened.
  • Those who agree to use double protective contraceptive measures from one days before administration of first investigative drug to last follow-up visit(protective contraceptive measures using more than 2 ways among a male condom, a female condom of sex partner, a spermicide of sex partner, an intrauterine device(IUD) of sex partner, a diaphragm of sex partner and a cervical cap of sex partner), and not to provide sperm.
  • Those who voluntarily decide to follow matters that require attention of this study and give written consent to participate in this clinical trial.
  • Those who can visit the medical center to be monitored, and agree to collect blood during study period.

Exclusion Criteria:

  • Those who have GC1102 anti-body when screened
  • Those who have a clinically meaningful disease or history concerning liver, kidney, alimentary system, respiratory system, musculoskeletal system, endocrine system, neuropsychiatry system, blood tumor system, cardiovascular system.
  • Those who have anaphylaxis of drug allergy including HBIG or who have allergy disease requiring treatment.
  • Those who have immunodeficiency disease now.
  • Those who have an anamnesis of Guillain-Barre syndrome.
  • Hemophiliac patients who have a risk of serious bleeding when getting a shot through intravascular injection or those who are being administered anticoagulants
  • Those who are administered live vaccine parenterally within 120 days from being administered first investigative drug. (ex: measles vaccine, epidemic parotitis vaccine, rubella vaccine, cholera vaccine, chickenpox vaccine)
  • Those who are administered interferon or antiviral agents within 120 days from being administered first investigative drug. (except for topical medication)
  • Those who showed signs of an acute fever(over 38℃) within 72 hours from being administered first investigative drug.
  • Those who showed signs of acute disease within 14 days from being administered first investigative drug.
  • Those who donated whole blood within 60 days or ingredient blood within 30 days from being administered first investigative drug or those who are administered blood transfusion within 30 days from being administered first investigative drug.
  • Those who took other investigative drugs within 60 days from being administered first investigative drug.
  • Those who took herbal medicine within 30 days from being administered first investigative drug or took ethical drug(ETC) within 14 days or took over-the- counter drug(OTC) within 7 days from being administered first investigative drug.(but, Those who meet other conditions can join the clinical trials according to investigator's decision)
  • Those who drink excessively caffeine-contained beverage, excessive alcohol, and who are smokers( caffeine> 5 units/ day, alcohol>21 units/ week, cigarette> 10 pieces) or have a history of alcoholism
  • Those who have a history of drug addiction, or showed positive response of urine-drug screening examination (ex: amphetamine, methamphetamine, barbiturate, cocaine, opiate, benzodiazepines, cannabinoid, methadone, etc)
  • Those who showed positive sign of serum test(A-type hepatitis test(HAV IgM Ab), C-type hepatitis test(HCV Ab screening), HIV test(HIV Ag & Ab), Syphilis high quality reagin test.
  • Those whose serum creatinine, ALT, AST, or total bilirubin exceeded the standard 1.5 times by the diagnostic lab test.
  • Those who cannot eat standard meals provided by Seoul Asan medical center.
  • Those who are judged disqualified to join clinical trials by investigator for other causes.

Sites / Locations

  • Department of clinical pharmacology and therapeutics

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

group 1

group 2

group 3

group 4

Arm Description

Drug:GC1102 Amount:3ml (30,000IU)

Drug: GC1102 Amount: 5ml(50,000IU)

Drug: GC1102 Amount: 8ml (80,000IU)

drug: JW normal saline

Outcomes

Primary Outcome Measures

Safety of GC1102 when repeatedly administered by intravenous injection to healthy male adults
Adverse event Diagnostic examinations Physical examinations Vital signs ECG(electrocardiogram) Check of concomitant drug

Secondary Outcome Measures

Pharmacokinetics of GC1102 when repeatedly administered by intravenous injection to healthy male adults
Terminal elimination half-life (t½β) Maximum and Average concentration at steady state(Cmax,ss, Cav,ss,) Area-under the concentration-time curve within a dosing interval at steady state (AUCτ,ss) Clearance (CL) Volume of distribution at steady state (Vd,ss) Mean residence time (MRT) Accumulation Index (AI)

Full Information

First Posted
May 23, 2012
Last Updated
January 1, 2014
Sponsor
Green Cross Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT01606163
Brief Title
Safety and Pharmacokinetics Study of Healthy Male Adults When Repeatedly Administered Through Intravenous Injection
Official Title
A Phase 1, Randomized, Double-blind, Placebo-controlled, Multiple-dose, Dose Escalation Study to Assess the Safety and Pharmacokinetics of GC1102 (Hepabig-Gene) in Healthy Male Adults
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Green Cross Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the safety and pharmacokinetics of healthy male adults when subjects are repeatedly administered GC1102 (Hepabig_Gene) through intravenous injection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Arm Title
group 1
Arm Type
Experimental
Arm Description
Drug:GC1102 Amount:3ml (30,000IU)
Arm Title
group 2
Arm Type
Experimental
Arm Description
Drug: GC1102 Amount: 5ml(50,000IU)
Arm Title
group 3
Arm Type
Experimental
Arm Description
Drug: GC1102 Amount: 8ml (80,000IU)
Arm Title
group 4
Arm Type
Placebo Comparator
Arm Description
drug: JW normal saline
Intervention Type
Biological
Intervention Name(s)
GC1102
Other Intervention Name(s)
Hepabig_Gene
Intervention Description
Description: GC1102 IV bolus injection during 10~ 30 seconds. Amount: group1-3ml, group2-5ml, group3-8ml Subject number: group1-8, group2-8, group3-8 Administration time: 1day, 2day, 3day, 4day, 5day, 6day, 7day(total: 7 times)
Intervention Type
Other
Intervention Name(s)
JW normal saline
Other Intervention Name(s)
saline solution
Intervention Description
Description: Normal saline IV bolus injection through 10~ 30 seconds. Each 3 subjects of this placebo comparator group will match with group 1,2,3 respectively. Placebo comparator subjects in each group will be treated with same condition of each group(group 1, group 2, group 3) except being administered JW normal saline. Subject number: 9 Administration time: 1day, 2day, 3day, 4day, 5day, 6day, 7day(total: 7 times)
Primary Outcome Measure Information:
Title
Safety of GC1102 when repeatedly administered by intravenous injection to healthy male adults
Description
Adverse event Diagnostic examinations Physical examinations Vital signs ECG(electrocardiogram) Check of concomitant drug
Time Frame
screening, -1d, 1d, 2d, 3d, 4d, 5d, 6d, 7d, 8d, 9d, 14d, 21d, 28d
Secondary Outcome Measure Information:
Title
Pharmacokinetics of GC1102 when repeatedly administered by intravenous injection to healthy male adults
Description
Terminal elimination half-life (t½β) Maximum and Average concentration at steady state(Cmax,ss, Cav,ss,) Area-under the concentration-time curve within a dosing interval at steady state (AUCτ,ss) Clearance (CL) Volume of distribution at steady state (Vd,ss) Mean residence time (MRT) Accumulation Index (AI)
Time Frame
1)1d:predose(0h), 0.5, 1, 2, 5, 9, 14 hours after dose 2) 2d~6d:predose(0h) 3) 7d:predose(0h), 0.5, 1, 2, 5, 9, 14 hours after dose 4) 8d, 9d, 14d, 21d, 28d: 0h

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Those who are healthy, male adult aged 20 years- 45 years when screened. Those whose body weights are over 45kg when screened, and whose BMI scores are 19kg/㎡-28 kg/㎡. Those whose HBs-Ag, HBc-Ab(IgM), HBc-Ab(IgG), HBV DNA quantitative are all negative when screened. Those whose HBs-Ab(titer) in blood is below 500 IU/L when screened. Those who agree to use double protective contraceptive measures from one days before administration of first investigative drug to last follow-up visit(protective contraceptive measures using more than 2 ways among a male condom, a female condom of sex partner, a spermicide of sex partner, an intrauterine device(IUD) of sex partner, a diaphragm of sex partner and a cervical cap of sex partner), and not to provide sperm. Those who voluntarily decide to follow matters that require attention of this study and give written consent to participate in this clinical trial. Those who can visit the medical center to be monitored, and agree to collect blood during study period. Exclusion Criteria: Those who have GC1102 anti-body when screened Those who have a clinically meaningful disease or history concerning liver, kidney, alimentary system, respiratory system, musculoskeletal system, endocrine system, neuropsychiatry system, blood tumor system, cardiovascular system. Those who have anaphylaxis of drug allergy including HBIG or who have allergy disease requiring treatment. Those who have immunodeficiency disease now. Those who have an anamnesis of Guillain-Barre syndrome. Hemophiliac patients who have a risk of serious bleeding when getting a shot through intravascular injection or those who are being administered anticoagulants Those who are administered live vaccine parenterally within 120 days from being administered first investigative drug. (ex: measles vaccine, epidemic parotitis vaccine, rubella vaccine, cholera vaccine, chickenpox vaccine) Those who are administered interferon or antiviral agents within 120 days from being administered first investigative drug. (except for topical medication) Those who showed signs of an acute fever(over 38℃) within 72 hours from being administered first investigative drug. Those who showed signs of acute disease within 14 days from being administered first investigative drug. Those who donated whole blood within 60 days or ingredient blood within 30 days from being administered first investigative drug or those who are administered blood transfusion within 30 days from being administered first investigative drug. Those who took other investigative drugs within 60 days from being administered first investigative drug. Those who took herbal medicine within 30 days from being administered first investigative drug or took ethical drug(ETC) within 14 days or took over-the- counter drug(OTC) within 7 days from being administered first investigative drug.(but, Those who meet other conditions can join the clinical trials according to investigator's decision) Those who drink excessively caffeine-contained beverage, excessive alcohol, and who are smokers( caffeine> 5 units/ day, alcohol>21 units/ week, cigarette> 10 pieces) or have a history of alcoholism Those who have a history of drug addiction, or showed positive response of urine-drug screening examination (ex: amphetamine, methamphetamine, barbiturate, cocaine, opiate, benzodiazepines, cannabinoid, methadone, etc) Those who showed positive sign of serum test(A-type hepatitis test(HAV IgM Ab), C-type hepatitis test(HCV Ab screening), HIV test(HIV Ag & Ab), Syphilis high quality reagin test. Those whose serum creatinine, ALT, AST, or total bilirubin exceeded the standard 1.5 times by the diagnostic lab test. Those who cannot eat standard meals provided by Seoul Asan medical center. Those who are judged disqualified to join clinical trials by investigator for other causes.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kyun-Seop Bae, MD, PhD
Organizational Affiliation
Department of clinical pharmacology and therapeutics
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of clinical pharmacology and therapeutics
City
Seoul
ZIP/Postal Code
138-736
Country
Korea, Republic of

12. IPD Sharing Statement

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Safety and Pharmacokinetics Study of Healthy Male Adults When Repeatedly Administered Through Intravenous Injection

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