Autoinjector Device Assessment Study (BCB119)

Evaluation of the Single-Use Pre-Filled Autoinjector

Phase I study to determine the device-related injection failure rate of the single-use, pre-filled autoinjector.

Study Overview

• Status: Completed
• Conditions: Healthy Subjects
• Intervention / Treatment: Drug: Auto-injector with exenatide suspension; Drug: Syringe with exenatide suspension

Detailed Description

Phase I multi-cohort study will employ a flexible study design to accommodate multiple cohorts. Healthy male or female subjects >or= 18 years with no significant health issues will be included. Each cohort will employ an open-label, single-arm, repeat-dose design. Injection failure rates will be continually assessed. Injection pain will also be assessed.

• Study Type: Interventional
• Enrollment (Actual): 3052
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Arizona
    • Tempe, Arizona, United States
      • Research Site
  • Nebraska
    • Lincoln, Nebraska, United States
      • Research Site

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Is at least 18 years old at Visit 1 (Screening). Subjects must be of legal age of consent.
• Has no significant health issues that would preclude study participation, as determined by medical history and physical examination
• Has body mass index of 22 kg/m2 to 45 kg/m2, inclusive, at Visit 1 (Screening)
• Has normal renal function (creatinine clearance adjusted for body surface area ≥90 mL/min/1.73 m2 as calculated using the MDRD equation) at Visit 1 (Screening)

• Is male, or is female and meets all the following criteria:

  1. Not breastfeeding
  2. Negative pregnancy test result (human chorionic gonadotropin, beta subunit [bhCG]) at Visit 1 (Screening)
  3. If of childbearing potential (including perimenopausal women who have had a menstrual period within 1 year), must practice and be willing to continue to practice appropriate birth control (defined as a method which results in a low failure rate, i.e., less than 1% per year, when used consistently and correctly, such as implants, injectables, hormonal contraceptives, some intrauterine contraceptive devices, sexual abstinence, tubal ligation or occlusion, or a vasectomized partner) during the entire duration of the study. Subjects must practice appropriate birth control as stated above for 10 weeks after the last dose of study drug.
• Has no clinically significant abnormal laboratory test values (clinical chemistry, hematology, urinalysis) as judged by the investigator at Visit 1 (Screening)
• Has a physical examination and electrocardiogram (ECG) with no clinically significant abnormality, as judged by the investigator, at Screening
• Is able to read, understand, and sign the Informed Consent Forms (ICFs) and, if applicable, an Authorization to Use and Disclose Protected Health Information form (consistent with Health Insurance Portability and Accountability Act of 1996 [HIPAA] legislation), communicate with the investigator, and understand and comply with protocol requirements

Exclusion Criteria:

• Has a clinically significant medical condition that could potentially affect study participation and/or personal well-being, as judged by the investigator, including but not limited to the following conditions:

  1. History of, or currently have, acute or chronic pancreatitis, or have triglyceride concentrations

     • 500 mg/dL at Visit 1 (Screening)
  2. Presence of medullary carcinoma or multiple endocrine neoplasia (MEN II) OR a family history of medullary carcinoma or MEN II
  3. Organ transplantation
  4. Active cardiovascular disease within 3 months of Visit 1 such as myocardial infarction, clinically significant arrhythmia, unstable angina, coronary artery bypass surgery, or angioplasty; or are expected to require coronary artery bypass surgery or angioplasty during the course of the study. Subjects with stable cardiac disease are not excluded.
  5. Presence or history of severe congestive heart failure (New York Heart Association Class IV [CCNYHA 1994])
  6. Central nervous system disease, including epilepsy (individuals with a history of convulsions associated with hypoglycemia will not be excluded)
  7. Liver disease, acute or chronic hepatitis, alanine aminotransaminase (ALT), or serum glutamic pyruvic transaminase (SGPT) greater than 3 times the upper limit of the reference range
  8. History or presence of inflammatory bowel disease or other severe gastrointestinal diseases, particularly those which may impact gastric emptying, such as gastroparesis, pyloric stenosis, gastric bypass surgery or gastric banding surgery
  9. Clinically significant malignant disease (with the exception of basal and squamous cell carcinoma of the skin) within 5 years of Visit 1 (Screening)
  10. Hemoglobinopathy, hemolytic anemia, or anemia (hemoglobin concentration below the lower limit of normal unless deemed not clinically significant by the investigator)
  11. Two or more episodes of severe hypoglycemia within 6 months prior to Visit 1. Refer to Section 9.1.5.2 for more information on hypoglycemia
  12. Evidence of acute or chronic illness including known or suspected human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV) infection
• Has any abdominal skin abnormalities (e.g., extensive scarring, burns, inflammation, hyperkeratosis, etc.) which, in the investigator's opinion, could interfere with the injection.
• Has serum calcitonin concentration ≥100 pg/mL at Visit 1 (Screening)
• Has evidence of current abuse of drugs or alcohol or a history of abuse that, in the investigator's opinion, would cause the individual to be noncompliant
• Has a positive urine drug screen (including screen for cocaine, opiates, amphetamines, and cannabinoids)
• Has received any investigational drug within 30 days (or 5 half-lives of the investigational drug, whichever is greater) prior to Visit 1 (Screening)
• Has donated blood or had a significant blood loss within 2 months of first dose of study drug or is planning to donate blood during the study
• Has had a major surgery or a blood transfusion within 2 months prior to Visit 1 (Screening)
• Has known contraindication, allergies, or hypersensitivity to any component of study drug (including poly-D,L lactide co-glycolide [PLG] and MCT)
• Is employed by Amylin, Alkermes, Bristol-Myers Squibb, or AstraZeneca (i.e. that is an employee, temporary contract worker, or designee responsible for the conduct of the study)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

5

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Arm 1; exenatide suspension - 9 mg / 0.85 mL	Drug: Auto-injector with exenatide suspension; A flexible study design to accommodate multiple cohorts.
Experimental: Arm 2; exenatide suspension - 9 mg / 0.85 mL	Drug: Syringe with exenatide suspension; A flexible study design to accommodate multiple cohorts.
Experimental: Arm 3; exenatide suspension - 4.5 mg /1.1 mL	Drug: Syringe with exenatide suspension; A flexible study design to accommodate multiple cohorts.
Experimental: Arm 4; exenatide suspension - 9 mg / 1.1 mL	Drug: Syringe with exenatide suspension; A flexible study design to accommodate multiple cohorts.
Experimental: Arm 5; exenatide suspension - 9 mg / 1.5 mL	Drug: Syringe with exenatide suspension; A flexible study design to accommodate multiple cohorts.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of device-related failure injections	The primary outcome measure is the number of device-related injection failures of the single-use, pre-filled auto-injector.	10 week study

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of device-related injection failures of alternate device configuration	The secondary outcome measure is the number of device-related injection failures of alternate device configuration.	10 week study

Collaborators and Investigators

• Sponsor: AstraZeneca
• Collaborators: Celerion
• Investigators: Principal Investigator: Peter Davidson, DO, Celerion; Study Director: Elise Hardy, MD, AstraZeneca

Publications and helpful links

Helpful Links

• D5554C00001_CSR_Synopsis

Study record dates

Study Major Dates

• Study Start: February 1, 2013
• Primary Completion (Actual): December 1, 2013
• Study Completion (Actual): December 1, 2013

Study Registration Dates

• First Submitted: January 26, 2015
• First Submitted That Met QC Criteria: January 26, 2015
• First Posted (Estimate): January 29, 2015

Study Record Updates

• Last Update Posted (Estimate): February 2, 2015
• Last Update Submitted That Met QC Criteria: January 29, 2015
• Last Verified: January 1, 2015

More Information

Terms related to this study

• Keywords: Auto-injector Device, device-related injection, Auto-injector
• Additional Relevant MeSH Terms: Hypoglycemic Agents; Physiological Effects of Drugs; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Anti-Obesity Agents; Incretins; Exenatide
• Other Study ID Numbers: D5554C00001