A Study to Evaluate the Safety, Tolerability and Immunogenicity of Two Vaccinations of Ad26.RSV.preF One Year Apart in Adults Aged 60 Years and Older in Stable Health

NCT02926430 | Completed Phase 1

• 2 other identifiers: CR108214VAC18193RSV1003
• Study Type: interventional
• Target: 73
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to assess the safety and tolerability of 2 single doses of either 5\*10\^10 viral particles (vp) or 1\*10\^11 vp of Ad26.RSV.preF, administered intramuscularly to elderly adults given approximately 12 months apart.

Conditions

Healthy

Outcome Measures

Primary Outcomes (6)

• Number of Participants With Solicited Local Adverse Events (AEs) for 7 Days After Each Vaccination (Day 1)

  7 days after each vaccination (Day 1)

• Number of Participants With Solicited Local Adverse Events (AEs) for 7 Days After Each Vaccination (Day 365)

  7 days after each vaccination (Day 365)

• Number of Participants With Solicited Systemic Adverse Events (AEs) for 7 Days After Each Vaccination (Day 1)

  7 days after each vaccination (Day 1)

• Number of Participants With Solicited Systemic Adverse Events (AEs) for 7 Days After Each Vaccination (Day 365)

  7 days after each vaccination (Day 365)

• Number of Participants With Unsolicited AEs for 28 Days After Each Vaccination

  28 days after each vaccination (from signing the informed consent form [ICF] to Day 29 inclusive)

• Number of Participants With Serious Adverse Events (SAEs) Throughout Study

  Up to 730 days

Secondary Outcomes (3)

• Respiratory Syncytial Virus (RSV) Neutralization A2

  Days 1, 29, 183, 365, 393, 547, 730

• RSV Fusion Protein (F-protein) Enzyme-linked Immunosorbent Assay

  Days 1, 29, 183, 365, 393, 547, 730

• Intracellular Cytokine Staining

  Day 1, 29, 183, 365, 393, 547, 730

Study Arms (5)

Ad26.RSV.preF 5*10^10 vp (Day 1 and Day 365): Group 1

EXPERIMENTAL

Participants will receive 5\*10\^10 viral particles (vp) Ad26.RSV.preF at Day 1 and Day 365 (10 to 13 months after first vaccination).

Biological: Ad26.RSV.preF 5*10^10 vp

Ad26.RSV.preF 5*10^10 vp (Day 1)- Placebo (Day 365): Group 2

EXPERIMENTAL

Participants will receive 5\*10\^10 vp Ad26.RSV.preF at Day 1 and placebo on Day 365 (10 to 13 months after first vaccination).

Biological: Ad26.RSV.preF 5*10^10 vp; Drug: Placebo

Ad26.RSV.preF 1*10^11 vp (Day 1 and Day 365): Group 3

EXPERIMENTAL

Participants will receive 1\*10\^11 vp Ad26.RSV.preF at Day 1 and Day 365 (10 to 13 months after first vaccination).

Biological: Ad26.RSV.preF 1*10^11 vp

Ad26.RSV.preF 1*10^11 vp (Day 1)- Placebo (Day 365): Group 4

EXPERIMENTAL

Participants will receive 1\*10\^11 vp Ad26.RSV.preF at Day 1 and placebo on Day 365 (10 to 13 months after first vaccination).

Biological: Ad26.RSV.preF 1*10^11 vp; Drug: Placebo

Placebo (Day 1 and Day 365): Group 5

EXPERIMENTAL

Participants will receive placebo at Day 1 and Day 365 (10 to 13 months after first vaccination).

Drug: Placebo

Interventions

Ad26.RSV.preF 5*10^10 vp BIOLOGICAL

Ad26.RSV.preF will be given at a concentration of 5\*10\^10 vp/0.5 milliliter (mL).

Also known as: JNJ-64400141

Ad26.RSV.preF 5*10^10 vp (Day 1 and Day 365): Group 1; Ad26.RSV.preF 5*10^10 vp (Day 1)- Placebo (Day 365): Group 2

Ad26.RSV.preF 1*10^11 vp BIOLOGICAL

Ad26.RSV.preF will be given at a concentration of 1\*10\^11 vp/0.5 milliliter (mL).

Also known as: JNJ-64400141

Ad26.RSV.preF 1*10^11 vp (Day 1 and Day 365): Group 3; Ad26.RSV.preF 1*10^11 vp (Day 1)- Placebo (Day 365): Group 4

Placebo DRUG

Participants will receive placebo as formulation buffer.

Ad26.RSV.preF 1*10^11 vp (Day 1)- Placebo (Day 365): Group 4; Ad26.RSV.preF 5*10^10 vp (Day 1)- Placebo (Day 365): Group 2; Placebo (Day 1 and Day 365): Group 5

Eligibility Criteria

• Age: 60 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Each participant must sign an informed consent form (ICF) indicating that he or she understands the purpose of and procedures required for the study, is willing to participate in the study and attend all scheduled visits, and is willing and able to comply with all study procedures and adhere to the prohibitions and restrictions specified in this protocol
• Before randomization, a woman must be: postmenopausal - A postmenopausal state is defined as no menses for 12 months without an alternative medical cause; and not intending to conceive by any methods
• From the time of first vaccination until 3 months after the first dose of study vaccine, and from the second vaccination through 3 months after, a man who has not had a vasectomy (or if a vasectomy was performed less than 1 year ago and the absence of sperm cannot be verified)
• In the investigator's clinical judgment, participant must be either in good or stable health. Participants may have underlying illnesses such as hypertension, type 2 diabetes, hyperlipoproteinemia, or hypothyroidism, as long as their symptoms/signs are medically controlled. If they are on medication for a condition, the medication dose must have been stable for at least 12 weeks preceding vaccination and expected to remain stable for the duration of the study. Participants will be included on the basis of physical examination, medical history, vital signs, and 12-lead electrocardiogram (ECG) performed at screening
• Participant must be healthy on the basis of clinical laboratory tests performed at screening. If the results of the laboratory screening tests are outside the central laboratory normal reference ranges and additionally within the limits of toxicity Grades 1 or 2 according to the US Food and Drug Administration (FDA) toxicity tables (for tests in the FDA table ), the participant may be included only if the investigator judges the abnormalities or deviations from normal to be not clinically significant and appropriate and reasonable for the population under study. This determination must be recorded in the participant's source documents and initialed by the investigator

You may not qualify if:

• Participant has acute illness (this does not include minor illnesses such as diarrhea) or temperature greater than or equal to (\>=) 38.0 degree celsius within 24 hours prior to the first dose of study vaccine; enrollment at a later date is permitted
• Participant has a serious chronic disorder, including severe chronic obstructive pulmonary disease or clinically significant congestive heart failure, requirement for supplemental oxygen, end stage renal disease with or without dialysis, clinically unstable cardiac disease, Alzheimer's disease, or has any condition for which, in the opinion of the investigator, participation would not be in the best interest of the participant (for example, compromise well-being) or that could prevent, limit, or confound the protocol-specified assessments
• Participant has had major surgery within the 4 weeks prior to randomization or has planned major surgery through the course of the study
• Participant has chronic active hepatitis B or hepatitis C infection, documented by hepatitis B surface antigen and hepatitis C antibody, respectively
• Participant has human immunodeficiency virus (HIV) type 1 or type 2 infection

Sponsors & Collaborators

• Janssen Vaccines & Prevention B.V.: lead

Study Sites (1)

Unknown Facility

Miami, Florida, United States

Location

Study Officials

• Janssen Vaccines & Prevention B.V. Clinical Trial

  Janssen Vaccines & Prevention B.V.

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, CARE PROVIDER
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 22, 2016
• First Posted: October 6, 2016
• Study Start: November 8, 2016
• Primary Completion: March 14, 2018
• Study Completion: January 29, 2019
• Last Updated: February 19, 2019

Record last verified: 2019-02

Locations

US (1)