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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/show/NCT01505491




Registration number
NCT01505491
Ethics application status
Date submitted
4/01/2012
Date registered
4/01/2012
Date last updated
12/12/2012

Titles & IDs
Public title
Pharmacokinetics and Safety Study of BI 695501 in Healthy Subjects
Scientific title
Pharmacokinetics and Safety of BI 695501 in Healthy Subjects: a Randomized, Open-label, Single Dose, Parallel Arm, Active Comparator Clinical Phase I Study
Secondary ID [1] 0 0
1297.1
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
Treatment: Drugs - adalimumab
Treatment: Drugs - BI695501
Treatment: Drugs - adalimumab

Experimental: BI 695501 - Subject to receive one subcutaneous (s.c.) injection from a prefilled syringe containing BI 695501

Active Comparator: adalimumab - US - Subject to receive one s.c. injection from a prefilled syringe containing 40mg adalimumab

Active Comparator: adalimumab - EU - Subject to receive one s.c. injection from a prefilled syringe containing 40mg adalimumab


Treatment: Drugs: adalimumab
40mg adalimumab single s.c. injection

Treatment: Drugs: BI695501
BI 695501 single s.c injection

Treatment: Drugs: adalimumab
40mg adalimumab single s.c. injection

Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity
Timepoint [1] 0 0
72 days
Primary outcome [2] 0 0
Maximum measured concentration of the analyte in plasma
Timepoint [2] 0 0
72 days
Secondary outcome [1] 0 0
Area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the time of the last quantifiable data point
Timepoint [1] 0 0
72 days
Secondary outcome [2] 0 0
Area under the concentration-time curve of the analyte in plasma over the time interval from 0 to 14
Timepoint [2] 0 0
72 days
Secondary outcome [3] 0 0
Terminal phase half life
Timepoint [3] 0 0
72 days
Secondary outcome [4] 0 0
Apparent clearance of the analyte in the plasma after extravascular administration
Timepoint [4] 0 0
72 days

Eligibility
Key inclusion criteria
Inclusion criteria:

1. Healthy males

2. Body mass index (BMI) =18.5 to =29.9 kg/m2
Minimum age
18 Years
Maximum age
55 Years
Gender
Males
Can healthy volunteers participate?
Yes
Key exclusion criteria
Exclusion criteria:

1. Any clinically relevant abnormal finding of the medical examination (including blood
pressure, pulse rate and electrocardiogram) deviating from normal and of clinical
relevance

2. Any evidence of a clinically relevant previous or concomitant disease as judged by the
investigator.

3. Chronic or relevant acute infections. A negative result for Human Immunodeficiency
Virus, Hepatitis B and Hepatitis C testing is required for participation.

4. History of relevant allergy/hypersensitivity (including allergy to drug or its
excipients)

5. Intake of prescribed or over-the-counter drugs with a long half-life (>24 hours)
within at least one month or less than 5 half-lives of the respective drug prior to
administration or during the trial

6. Smoker (> 10 cigarettes or > 3 cigars or > 3 pipes/day)

7. Inability to refrain from smoking during days of confinement at the study center

8. Alcohol abuse (average more than 30 g/day)

9. Current drug abuse

Study design
Purpose of the study
Treatment
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
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
New Zealand
State/province [1] 0 0
Auckland
Country [2] 0 0
New Zealand
State/province [2] 0 0
Christchurch

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Boehringer Ingelheim
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This trial will investigate the pharmacokinetics, safety and tolerability of BI 695501 and to
establish pharmacokinetic equivalence of BI 695501 to adalimumab.
Trial website
https://clinicaltrials.gov/show/NCT01505491
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Boehringer Ingelheim
Address 0 0
Boehringer Ingelheim
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

No data has been provided for results reporting
Summary results
Other publications