Purpose

The purpose of this study is to evaluate the safety and tolerability of three dose levels of ASP3772 in comparison to the active comparator Prevnar 13® (PCV13) in toddlers who have previously been administered the routine three-dose series of PCV13. This study will also evaluate the immunogenicity (production of an immune response) of three different dose levels of ASP3772 in comparison to the active comparator PCV13 in toddlers who have previously been administered the routine three-dose series of PCV13.

Conditions

Eligibility

Eligible Ages
Between 12 Months and 15 Months
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Subject is a healthy toddler who has previously completed a 3-dose infant series of PCV13 with the last vaccination greater than 2 months prior to study vaccination. - Subject is afebrile within the last 48 hours (temperature measured orally is < 100 °F [37.8°C]; measured rectally or tympanic is < 101 °F [38.3°C]; measured in an axillary position or temporal is < 98.4 °F [36.9°C]). - Subject's parent/legal guardian is able to read, understand and complete study questionnaires (i.e., the electronic subject diary device). - Subject's parent/legal guardian along with the subject is able and is willing to attend all scheduled visits and to comply with the study procedures. - Subject's parent/legal guardian has access to a telephone. - Subject's parent/legal guardian agrees not to enroll subject in another interventional study while participating in the present study.

Exclusion Criteria

  • Subject has a known hypersensitivity to any vaccine. - Subject has an immune disorder(s) (including autoimmune disease) and/or clinical conditions requiring immunosuppressive drugs, known or suspected impairment of immunological function or a history of congenital or acquired immunodeficiency. - Subject has or his/her mother has known human immunodeficiency virus infection or known to be hepatitis B surface antigen-positive. - Subject has functional or anatomic asplenia. - Subject has known neurological or cognitive behavioral disorders including clinically significant developmental disorder and related disorders. - Subject has any evidence of any unstable or active clinically significant cardiovascular, gastrointestinal, endocrine, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal and/or other major disease. - Subject has any active malignancy or history of malignancy. - Subject has been in receipt of intramuscular, oral, intravenous, inhaled or intranasal corticosteroid treatment within 2 weeks prior to study vaccination or is planned to receive these medications within 4 weeks after study vaccination. Note: Use of topical corticosteroids is permitted. - Subject has received any live-attenuated vaccines within 4 weeks prior to receipt of the study vaccine or inactivated vaccines within 2 weeks prior to receipt of study vaccine. - Subject has previously received an approved (other than PCV13) or investigational pneumococcal vaccine. - Subject has had any prior receipt of a blood transfusion or blood products, including immunoglobulins. - Subject has received investigational therapy within 30 days or 5 half-lives, whichever is longer, prior to screening. - Subject has received a systemically absorbed antibacterial agent within 7 days prior to study vaccination. - Subject has a history of microbiologically-proven invasive disease caused by S. pneumoniae. - Subject has received acetaminophen or nonsteroidal anti-inflammatorydrugs (NSAIDs) within 24 hours prior to receipt of study vaccine. - Subject has a coagulation disorder. - Subject's parent/legal guardian is unlikely to adhere to study procedures, keep appointments, or is planning to relocate during the study and the subject cannot be adequately followed for safety according to the protocol. - Subject who has a condition which makes the subject unsuitable for study participation. - Subject's parent(s)/legal guardian is an employee of Astellas Pharma Global Development Inc., the study-related contract research organizations (CROs), or the study site.

Study Design

Phase
Phase 1
Study Type
Interventional
Allocation
Randomized
Intervention Model
Sequential Assignment
Primary Purpose
Prevention
Masking
Double (Participant, Care Provider)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Group 1, ASP3772 Low Dose
Participants will receive a single intramuscular injection of ASP3772 administered on Day 1 at a low-dose level.
  • Biological: ASP3772
    Intramuscular (IM) injection
Active Comparator
Group 1, PCV13 Comparator
Participants will receive a single intramuscular injection of the approved dose of PCV13 on Day 1.
  • Biological: PCV13
    Intramuscular injection
    Other names:
    • Prevnar 13
Experimental
Group 2, ASP3772 Medium Dose
Participants will receive a single intramuscular injection of ASP3772 administered on Day 1 at a medium-dose level.
  • Biological: ASP3772
    Intramuscular (IM) injection
Active Comparator
Group 2, PCV13 Comparator
Participants will receive a single intramuscular injection of the approved dose of PCV13 on Day 1.
  • Biological: PCV13
    Intramuscular injection
    Other names:
    • Prevnar 13
Experimental
Group 3, ASP3772 High Dose
Participants will receive a single intramuscular injection of ASP3772 administered on Day 1 at a high-dose level.
  • Biological: ASP3772
    Intramuscular (IM) injection
Active Comparator
Group 3, PCV13 Comparator
Participants will receive a single intramuscular injection of the approved dose of PCV13 on Day 1.
  • Biological: PCV13
    Intramuscular injection
    Other names:
    • Prevnar 13

Recruiting Locations

University of Texas Medical Branch
Galveston, Texas 77555

More Details

Status
Recruiting
Sponsor
Astellas Pharma Global Development, Inc.

Study Contact

Astellas Pharma Global Development, Inc.
800-888-7704
astellas.registration@astellas.com

Detailed Description

After screening, participants will be randomized to ASP3772 or PCV13 on Day 1. A single dose of ASP3772 will be administered on Day 1 as an injection into the right or left thigh muscle at one of three dose levels. The participants randomized to PCV13 will receive a single intramuscular injection of the approved dose of PCV13 into the right or left thigh muscle. All participants will remain at the study site for approximately 30 to 60 minutes following vaccination in order for study site personnel to evaluate any immediate reactions, if needed. The participant's parent/legal guardian will observe for reactions, including daily body temperature measurements and tolerability assessments, from Day 2 through Day 7 and record observed events in the electronic diary device. All participants will have study visits on Day 7 (+ 1 day) and Day 30 (± 5 days) post-vaccination. The Day 7 visit may be conducted on site or by telephone call.The end-of-study visit will occur on Day 180 (± 14 days), which will be a safety follow-up by telephone call.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.