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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02572245
Other study ID # B5381005
Secondary ID
Status Completed
Phase Phase 1
First received September 25, 2015
Last updated June 3, 2016
Start date January 2016
Est. completion date May 2016

Study information

Verified date June 2016
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This is a study comparing adalimumab Pfizer (PF-06410293) administered as a subcutaneous(SC) injection using a pre-filled syringe (PFS) or pre-filled pen in healthy adult subjects


Recruitment information / eligibility

Status Completed
Enrollment 164
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

1. Healthy female subjects and/or male subjects, who, at the time of screening, are between the ages of 18 and 55 years, inclusive. Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, complete physical examination including blood pressure and pulse rate measurement, 12 lead electrocardiogram (ECG), and clinical laboratory tests.

2. Body Mass Index (BMI) of 17.5 to 32 kg/m2; and a total body weight >50 kg (110 pounds).

3. Chest X ray with no evidence of current, active TB or previous (inactive) TB, fungal or general infections, heart failure, malignancy, or other clinically significant abnormalities taken at Screening or within 24 weeks prior to Day 1 and read by a qualified radiologist.

4. Female subjects of non childbearing potential must meet at least one of the following criteria: a. Achieved postmenopausal status, defined as follows: cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause; status may be confirmed by having a serum follicle stimulating hormone (FSH) level confirming the post menopausal state; b. Have undergone a documented hysterectomy and/or bilateral oophorectomy; c. Have medically confirmed ovarian failure.

All other female subjects (including females with tubal ligations) will be considered to be of childbearing potential.

Exclusion Criteria:

1. Evidence or history of clinically significant infectious, hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, autoimmune, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing).

2. Evidence or history of nervous system demyelinating diseases (including multiple sclerosis, optic neuritis, Guillain Barré syndrome).

3. History of relevant orthostatic hypotension, fainting spells or blackouts.

4. Previous history of cancer, except for adequately treated basal cell or squamous cell carcinoma of the skin

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Device:
PF-06410293 PFS
PF-06410293 40 mg administered subcutaneously by Prefilled syringe
PF-06410293 PFP
PF-06410293 40 mg administered subcutaneously by prefilled pen

Locations

Country Name City State
United States ICON Early Phase Services, LLC San Antonio Texas

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum serum concentration (Cmax) Day 1 - Day 15 No
Primary Area under the concentration curve (AUC 0-2wk) Day 1-Day 15 No
Secondary Injection site tolerability (Subject Assessment - Visual Analog Scale) - Mean Injection site pain over 24 hour period post dose Mean injection site pain over a 24 hour period post dose rated by subject on a visual analog scale (VAS), compared for injection by PFS or PFP, and for the 2 injection locations using each device Hour 0 (immediately after injection), 15 minutes, 1, 3, 8, 12 and 24 hours post injection Yes
Secondary Injection site tolerability (Blinded Safety Assessor - Modified Draize Scale) - Mean injection site tolerability over 24 hour post dose Mean injection site tolerability using the Modified Draize Scale Numerical Grade over 24 hours post dose rated by the blinded Safety Assessor, compared for injection by PFS or PFP, and for the 2 injection locations using each device 1, 3, 8, 12 and 24 hours post injection Yes
Secondary Time to reach the maximum serum concentration (Tmax) Day 1 - Day 43 No
Secondary AUC from time 0 to the last time point with quantifiable concentration (AUCT) Day 1 - Day 43 No
Secondary AUC extrapolated to infinity (AUC0 inf) Day 1 - Day 43 No
Secondary Volume of distribution (Vz/F), Day 1 - Day 43 No
Secondary Apparent clearance (CL/F) Day 1 - Day 43 No
Secondary Terminal half life (t1/2) Day 1 - Day 43 No
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