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Single Ascending Dose of ASP3772 Study in Japanese Healthy Male and Female Adults, and Single Ascending Dose Study of ASP3772 in Comparison With PPSV23 in Japanese Elderly Male and Female Subjects

Phase 1
Completed
Conditions
Healthy Volunteers
Interventions
Biological: PPSV23 (subcutaneous)
Biological: ASP3772 (intramuscular)
Biological: PPSV23 (intramuscular)
Biological: ASP3772 (subcutaneous)
Registration Number
NCT04265911
Lead Sponsor
Affinivax, Inc.
Brief Summary

The purpose of this study is to evaluate the safety and tolerability of 3 different dose levels of ASP3772 administered subcutaneously or intramuscularly to Japanese healthy adults 20 to 49 years of age.

This study will also evaluate the safety and tolerability of 3 different dose levels of ASP3772 administered subcutaneously or intramuscularly, in comparison to the active comparator 23-valent pneumococcal polysaccharide vaccine (PPSV23) in Japanese elderly subjects 65 to 85 years of age.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
126
Inclusion Criteria
  • Group 1: Subject is a healthy male or female between 20 and 49 years of age inclusive, at informed consent.
  • Group 2: Subject is a male or female between 65 and 85 years of age inclusive, at informed consent who is healthy or has chronic controlled, stable disease with no change in disease severity, medical therapy and no hospitalization history in last 12 weeks from informed consent as determined by medical history, physical examination, and laboratory data.
  • Female subject of non-childbearing potential; male subject not able to father children or who is able to father children and willing to use a highly effective method of contraception.
  • Subject agrees not to participate in another interventional study while participating in the present study.
  • Subject has a body mass index (BMI) range of 17.6 to 26.4 kg/m^2 inclusive in Group 1 and 15.4 to 28.6 kg/m^2 inclusive in Group 2, and body weight at least 50 kg for male and 40 kg for female at screening.
Exclusion Criteria
  • Subject has had previous vaccination with any licensed or investigational pneumococcal vaccine at any time.
  • Subject has a history of microbiologically-proven invasive disease caused by Streptococcus pneumoniae.
  • Subject has an immune disorder(s) (including autoimmune disease), clinical conditions requiring immunosuppressive drugs and/or a close relative who has congenital immunodeficiency.
  • Group 1: Subject has any illness that requires medication or treatment.
  • Group 2: Subject has any evidence of unstable or active clinically significant cardiovascular, gastrointestinal, endocrine, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal and/or other major disease, e.g., uncontrolled hypertension, uncontrolled diabetes, heart failure, uncontrolled chronic obstructive pulmonary disease, end-stage renal disease, malignancy which is active and requires treatment.
  • Subject has any clinically significant history of allergic conditions including drug allergies, asthma or anaphylactic reactions, but excluding untreated asymptomatic seasonal allergies just before study vaccine administration.
  • Subject has a positive serology test for hepatitis B surface antigen (HBsAg), hepatitis B core antibody (anti-HBc), hepatitis A virus antibodies (immunoglobulin M), hepatitis C virus antibodies (anti-HCV) or antigens/antibodies to human immunodeficiency virus (HIV) type 1 and/or type 2 at screening.
  • Subject has/had febrile illness or symptomatic of viral, bacterial (including upper respiratory infection) or fungal (excluding skin infection) infection within 7 days prior to day 1.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
PPSV23 (subcutaneous) in ElderlyPPSV23 (subcutaneous)Participants will receive a single subcutaneous injection of the standard dose of PPSV23 on Day 1.
ASP3772 ((intramuscular) in AdultsASP3772 (intramuscular)Participants will receive a single dose of ASP3772 administered as an intramuscular injection on Day 1 at one of three dose levels.
PPSV23 (intramuscular) in ElderlyPPSV23 (intramuscular)Participants will receive a single intramuscular injection of the standard dose of PPSV23 on Day 1.
ASP3772 (subcutaneous) in AdultsASP3772 (subcutaneous)Participants will receive a single dose of ASP3772 administered as an subcutaneous injection on Day 1 at one of three dose levels.
ASP3772 (subcutaneous) in ElderlyASP3772 (subcutaneous)Participants will receive a single dose of ASP3772 administered as an subcutaneous injection on Day 1 at one of three dose levels.
ASP3772 (intramuscular) in ElderlyASP3772 (intramuscular)Participants will receive a single dose of ASP3772 administered as an intramuscular injection on Day 1 at one of three dose levels
Primary Outcome Measures
NameTimeMethod
Percentage of participants reporting solicited local adverse reactionsUp to Day 7

Local reactions include pain, tenderness, erythema/redness, swelling, and induration. The reaction will be graded with 4-range grade: 1 (mild) to 4 (potentially life-threatening).

Percentage of participants with laboratory value abnormalities and/or adverse events (AEs)Up to Day 30

Percentage of participants with potentially clinically significant laboratory values.

Percentage of participants reporting solicited systemic adverse reactionsUp to Day 7

Systemic reactions include nausea, vomiting, diarrhea, headache, fever, fatigue and myalgia and arthralgia. Vital signs up to 7 days postvaccination are collected as systemic reactions. The reaction will be graded with 4-range grade: 1 (mild) to 4 (potentially life-threatening).

Percentage of participants with treatment emergent adverse events (TEAEs) including serious AEs (SAEs), medically attended adverse events (MAAEs), potentially immune mediated medical conditions (PIMMCs) and new onset chronic diseases (NOCDs)Up to Day 30

An adverse event (AE) is any untoward medical occurrence in a subject administered an investigational product (IP), and which does not necessarily have to have a causal relationship with this treatment. TEAE is defined as an AE occurring after study immunization to the last visit (up to 30 days post-vaccination if the study is discontinued for an individual subject). An IP-related TEAE is defined as any TEAE with a causal relationship assessed as "yes" by the investigator or subinvestigator.

Percentage of participants with vital sign abnormalities and/or adverse events (AEs)Up to Day 30

Percentage of participants with potentially clinically significant vital sign values.

Percentage of participants with electrocardiogram (ECG) abnormalities and/or Adverse Events (AEs)Up to Day 30

Percentage of participants with potentially clinically significant ECG values.

Percentage of participants with physical exam abnormalities and/or adverse events (AEs)Up to Day 30

Percentage of participants with potentially clinically significant physical exam values.

Secondary Outcome Measures
NameTimeMethod
Geometric mean fold rise (GMFR) in anticapsular PS IgG concentration on day 30 relative to pre-immunization contained in ASP3772On Day 30

PS IgG measure will be used to characterize the immunological response on Day 30 after administration of ASP3772.

GMC for pneumococcal serotype-specific anticapsular PS IgG for each serotype contained in PPSV23On Day 30

PS IgG measure measure will be used to characterize the immunological response on Day 30 after administration of PPSV23

Ratio of GMC for pneumococcal serotype-specific anticapsular PS IgG (each ASP3772 dose level/PPSV23)On Day 30

PS IgG measure will be used to characterize the immunological response on Day 30 after administration of ASP3772 and PPSV23.

Ratio of the OPA GMT (each ASP3772 dose level/PPSV23)On Day 30

OPA measure will be used to characterize the immunological response on Day 30 after administration of ASP3772 and PPSV23

GMFR in OPA titer on day 30 relative to pre-immunization contained in PPSV23On Day 30

OPA titer will be used to characterize the immunological response on Day 30 after administration of PPSV23

Proportion of subjects with a ≥ 4-fold increase relative to baseline in OPA titer for each serotype contained in PPSV23On Day 30

OPA titer will be used to characterize the immunological response on Day 30 after administration of PPSV23

Geometric mean concentration (GMC) for pneumococcal serotype-specific anticapsular polysaccharide immunoglobulin G (PS IgG) for each serotype contained in ASP3772On Day 30

PS IgG measure will be used to characterize the immunological response on Day 30 after administration of ASP3772.

GMFR in anticapsular PS IgG concentration on day 30 relative to pre-immunization contained in PPSV23On Day 30

PS IgG measure will be used to characterize the immunological response on Day 30 after administration of PPSV23

Geometric mean titer (GMT) for opsonophagocytic activity (OPA) for each serotype contained in ASP3772On Day 30

OPA measure will be used to characterize the immunological response on Day 30 after administration of ASP3772.

GMT for OPA for each serotype contained in PPSV23On Day 30

OPA measure will be used to characterize the immunological response on Day 30 after administration of PPSV23

GMFR in OPA titer on day 30 relative to pre-immunization contained in ASP3772On Day 30

OPA titer will be used to characterize the immunological response on Day 30 after administration of ASP3772.

Proportion of subjects with a ≥ 4-fold increase relative to baseline in OPA titer for each serotype contained in ASP3772On Day 30

OPA titer will be used to characterize the immunological response on Day 30 after administration of ASP3772.

Proportion of subjects with a ≥ 4-fold increase relative to baseline in pneumococcal serotype-specific anticapsular PS IgG concentration for each serotype contained in ASP3772On Day 30

PS IgG measure will be used to characterize the immunological response on Day 30 after administration of ASP3772.

Proportion of subjects with a ≥ 4-fold increase relative to baseline in pneumococcal serotype-specific anticapsular PS IgG concentration for each serotype contained in PPSV23On Day 30

PS IgG measure will be used to characterize the immunological response on Day 30 after administration of PPSV23

Trial Locations

Locations (1)

JP81001

🇯🇵

Fukuoka, Japan

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