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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT02326233




Registration number
NCT02326233
Ethics application status
Date submitted
22/12/2014
Date registered
29/12/2014
Date last updated
18/03/2019

Titles & IDs
Public title
Pharmacokinetics, Safety, and Tolerability Study of the Pen and PFS of SB5 in Healthy Subjects
Scientific title
A Randomised, Open-labelled, Two-arm, Parallel Group, Single-dose Study to Compare the Pharmacokinetics, Safety, and Tolerability of the Pre-filled Pen and PFS of SB5 in Healthy Subjects
Secondary ID [1] 0 0
2014-005178-12
Secondary ID [2] 0 0
SB5-G12-NHV
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Healthy 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Other interventions - Pen of SB5
Other interventions - PFS of SB5

Experimental: Pen of SB5 - Pen of SB5, single-dose of 40 mg via subcutaneous injection (study drug)

Active Comparator: PFS of SB5 - PFS of SB5, single-dose of 40 mg via subcutaneous injection (reference drug)


Other interventions: Pen of SB5


Other interventions: PFS of SB5
Intervention code [1] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Area Under the Concentration-time Curve From Time Zero to Infinity (AUCinf)
Timepoint [1] 0 0
0, 24, 48, 96, 120, 144, 168, 216, 264, 336, 408, 504, 600, 696, 840, 1008, and 1344 h postdose
Primary outcome [2] 0 0
Area Under the Concentration-time Curve From Time Zero to the Last Quantifiable Concentration (AUClast)
Timepoint [2] 0 0
0, 24, 48, 96, 120, 144, 168, 216, 264, 336, 408, 504, 600, 696, 840, 1008, and 1344 h postdose
Primary outcome [3] 0 0
Maximum Serum Concentration (Cmax)
Timepoint [3] 0 0
0, 24, 48, 96, 120, 144, 168, 216, 264, 336, 408, 504, 600, 696, 840, 1008, and 1344 h postdose
Secondary outcome [1] 0 0
Time to Reach Cmax (Tmax)
Timepoint [1] 0 0
0, 24, 48, 96, 120, 144, 168, 216, 264, 336, 408, 504, 600, 696, 840, 1008, and 1344 h postdose

Eligibility
Key inclusion criteria
- Healthy subjects

- Have a body mass index between 20.0 to 29.9 kg/m², inclusive.
Minimum age
18 Years
Maximum age
55 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
- History and/or current presence of clinical significant atopic allergy,
hypersensitivity or allergic reactions, also including known or suspected clinically
relevant drug hypersensitivity to any components of the test and reference
investigational product formulation or comparable drugs

- Active or latent Tuberculosis or who have a history of Tuberculosis

- History of invasive systemic fungal infections or other opportunistic infections

- Systemic or local infection, a known risk for developing sepsis and/or known active
inflammatory process

- Serious infection associated with hospitalisation and/or which required intravenous
antibiotics

- History of and/or current cardiac disease

- Have received live vaccine(s) within 4 weeks prior to Screening or who will require
live vaccine(s) between Screening and the subject's last visit

- Intake medication with a half-life > 24 h within 4 weeks or 10 half-lives of the
medication prior to investigational product administration

Study design
Purpose of the study
Other
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/06/2015
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/09/2015
Sample size
Target
Accrual to date
Final
190
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
Belgium
State/province [1] 0 0
Antwerpen
Country [2] 0 0
New Zealand
State/province [2] 0 0
Auckland

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Samsung Bioepis Co., Ltd.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
The purpose of this study is to compare the pharmacokinetics, safety, and tolerability of the
pre-filled pen and pre-filled syringe of SB5 in healthy subjects.
Trial website
https://clinicaltrials.gov/ct2/show/NCT02326233
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT02326233