A Study to Evaluate Pain, Tolerability, Safety, and Usability of a Single Self-administered Etrolizumab by Auto-injector in Healthy Participants



Status:Completed
Conditions:Healthy Studies
Therapuetic Areas:Other
Healthy:No
Age Range:18 - 65
Updated:8/6/2016
Start Date:December 2015
End Date:June 2016

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A PHASE 1, OPEN-LABEL, SINGLE-ARM STUDY IN HEALTHY SUBJECTS TO EVALUATE PAIN, TOLERABILITY, SAFETY, AND USABILITY OF A PREFILLED AUTOINJECTOR TO SELF-ADMINISTER ETROLIZUMAB SUBCUTANEOUSLY

This study is a multi-center, single-arm, open-label study in healthy participants to assess
the pain, tolerability, injection leakage, safety, and usability of a single
self-administered subcutaneous (SC) dose of etrolizumab. Some participants will receive
"needle-experience" training using a needle and syringe on Days -7 and -5, and health care
professionals (HCPs) will then assess the participant's suitability to self-inject with a
prefilled auto-injector (AI). The remainder of participants will be "needle naïve" and will
not have previously self-injected. Eligible" needle experienced" and" needle naive"
participants will attend an AI training visit at the study site on Day -3 (three days prior
to etrolizumab dosing on Day 1). Following training and simulated injections by the
participant the HCP will determine if the participant is suitable to proceed to actual
etrolizumab dosing. All eligible study participants will self administer a single dose of
etrolizumab (by AI) on Day 1 and will be followed up to Day 85 following dosing. Pain,
tolerability, safety and usuability will be assessed.


Inclusion Criteria:

- Males or females, between 18 and 65 years of age, inclusive

- Within body mass index (BMI) range 18.0 to 32.0 kilograms per square meter (kg/m^2),
inclusive

- In good health, determined by no clinically significant findings from medical
history, 12-lead electrocardiograms (ECGs), and vital signs

- Females will be non-pregnant, non-lactating, and either postmenopausal (at least 1
year of non therapy induced amenorrhea), surgically sterile (absence of ovaries
and/or uterus) for at least 90 days, or agree to remain abstinent or use a highly
effective method of contraception for at least 24 weeks after the single dose of
study drug

- Males will either be sterile or agree to remain abstinent or use a highly effective
method of contraception for at least 24 weeks after the single dose of study drug.
Male participants will refrain from sperm donation from Check-in (Day -1) until 24
weeks following study drug administration

Exclusion Criteria:

- Participation in any other investigational study drug or biological agent trial
(including investigational vaccines) in which receipt of an investigational study
drug occurred within 30 days or 5 half-lives or receipt of a biologic agent occurred
within 90 days or 5 half-lives, whichever is longer, prior to Check-in (Day -1) and
during the entire study

- Any prior treatment with etrolizumab or other anti integrin agents (including
natalizumab, vedolizumab, and efalizumab)

- Any prior exposure to immunosuppressive agents (e.g., methotrexate, azathoprine,
mercaptopurine)

- Use of IV steroids within 30 days prior to Screening;

- Chronic nonsteroidal anti inflammatory drug (NSAID)

- Use of any prescription medications/products within 14 days prior to Check in (Day
-1)

- History of demyelinating disease

- Neurological conditions or diseases

- History of cancer

- History of alcoholism or drug addiction within 1 year prior to Check-in (Day -1)

- History of active or latent tuberculosis (TB), regardless of treatment history

- History of recurrent opportunistic infections, severe disseminated viral infections
(e.g., herpes), or any serious opportunistic infection within the last 6 months

- Positive for human immunodeficiency virus (HIV) antibody

- Any current or recent signs or symptoms of infection

- Inability to sense pain (e.g., peripheral neuropathy) and have a history of or have
been diagnosed with a chronic pain syndrome
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