Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05421325

Efficacy of QBKPN Site-Specific Immunomodulator in Improving Innate Immune Function & Reducing Respiratory Tract Infection in Older Adults

This study is designed to test whether QBKPN SSI can improve immune function in older adults, including how well it can protect against respiratory and other infections, whether it improves the body's response to COVID-19 vaccines, what effect it has on maintaining or improving quality of life, activity level and health status and whether it has an effect on glycemic control.

QBKPN is a new medication in a class known as Site-Specific Immunomodulators (SSI). SSIs are designed to train and/or improve innate immune function to reduce the risk of infections, improve immune response to cancer, and slow the progression of chronic inflammatory diseases.

It is believed that QBKPN SSI can work with the immune system to help protect against respiratory and other infections.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Immune Deficiency Immune System Diseases Immunologic Deficiency Syndromes

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Qu Biologics Trial Site

Burnaby, British Columbia, V5G 4X4, Canada

Location status: Recruiting

Location contact

Alastair Teale, MD FRCPC

SUB_INVESTIGATOR

Boingotlo Masake, MD MSc FRCPC

SUB_INVESTIGATOR

Issa Ephtimios, MD FRCPC

SUB_INVESTIGATOR

Nimmy George, BSc

CONTACT

[email protected]

672-963-7872

Selena Bloom, MD MCFP SEP

SUB_INVESTIGATOR

Shannon Turvey, MD MSc MHA FRCPC

SUB_INVESTIGATOR

Theodore Steiner, MD FRCPC

PRINCIPAL_INVESTIGATOR

About this study

This is a randomized, double-blind, placebo-controlled study of adults 65 years of age or older residing in the community, in independent-living, assisted-living and long-term care (LTC) facilities to assess the effect of QBKPN SSI on improvement of innate immunity and reduction of all-cause respiratory tract infection morbidity.

Approximately 72 participants will be enrolled; approximately 36 from the community and independent-living facilities and approximately 36 from assisted-living and LTC facilities.

Eligible participants will be screened and enrolled by study staff, who will conduct all study visits, and administer or teach self-administration of study treatment. Blood/sample collections will be performed by study staff or by staff at Vancouver Coastal Health Research Institute Clinical Research Unit. Participants will have the options of nurse-administration, self-administration or a combination of nurse- and self-administration of study treatment. Participants will receive study treatment for 4 weeks then be monitored for 22 weeks. Blood/urine sampling will be performed at Baseline, Weeks 4, End of Treatment, Week 8, Week 12 and Week 26. A phone call visit will be conducted at Week 20.

Immunological testing for trained innate immunity, capacity for anti-viral innate immune response, measures of immune augmentation, duration of adaptive immune response to SARS-CoV-2 vaccination and/or infection, change in metabolome and Natural Killer (NK) cell function will be performed.

Safety and tolerability of study treatment will be assessed through clinical laboratory parameters and treatment-emergent adverse events.

Clinical benefits of study treatment will be assessed via medical record review and patient-reported outcomes. Study staff will record any confirmed/probable/possible infections (viral and bacterial, including respiratory and non-respiratory), any microbiologic or radiologic testing performed to investigate for infection, any prescribed antibiotics/antivirals and duration of treatment and reason for and duration of any hospitalizations.

Clinical assessments will also include frailty index (Rockwood Clinical Frailty Scale), quality of life [Dementia Quality of Life Questionnaire(DEMQOL)], end-of-life prediction score (CHESS Scale) and all-cause mortality.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be a resident of the community or a long-term care, independent-living or assisted living facility participating in the study
  • Be aged 65 years or older
  • Be able to provide written, informed consent themselves
  • Male subjects engaged in vaginal intercourse with women of childbearing potential must be surgically sterile or agree to practice effective barrier contraception during the entire study treatment period (4 weeks) and one month after the last dose of study drug or agree to completely abstain from vaginal intercourse with women of childbearing potential during this period.

Exclusion criteria

  • Life expectancy of less than 3 months due to terminal illness as determined by the Study Investigator
  • Taking biologic immunosuppressive agents (e.g., Anti-Tumour Necrosis Factor Alpha (anti-TNFa) antibodies, rituximab, ibrutinib, imatinib) calcineurin inhibitors, myelosuppressants (e.g., methotrexate, mycophenolate), or other systemic immunosuppressants. Note: NSAIDs, colchicine, aspirin and oral glucocorticoids at a dose equivalent to less than or equal to 5mg prednisone per day are allowed
  • Currently being treated or less than 30 days from being treated for confirmed or probable infection with systemic (i.e., not topical) antibiotics or antivirals
  • Have a known allergy or hypersensitivity to killed whole-cell bacterial vaccines
  • Any condition that, in the opinion of the Investigator, would preclude the person from participation in the study due to safety or monitoring concerns
  • Any treatment with experimental or investigational therapies within 3 months prior to Screening and/or any planned treatment with experimental or investigational therapies during the entire course of study participation
  • On current treatment for active malignancies (e.g., chemotherapy, radiation) or planned cancer surgery during the study period. Note: People on exclusively hormonal therapy for breast or prostate cancer are allowed. People with prior or planned surgery for localized squamous cell or basal cell carcinoma of the skin are allowed

Treatment and study plan

QBKPN SSI

Biological

Site-Specific Immunomodulator

Normal Saline Placebo

Other

Normal Saline

Primary outcomes

  1. Evaluate innate immune training in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to End of Treatment (EOT) (Week 4)

    Innate immune training will be measured by change in stimulated IL-β using RBM Myriad's TLR4 ligand (LPS) TruCulture Tube assay.

  2. Incidence of treatment-emergent adverse events (safety & tolerability) in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to EOT (Week 4) and Week 8

    Treatment-emergent adverse events assessed by Common Terminology Criteria for Adverse Events (CTCAE) v5.0.

  3. Change in clinical laboratory parameters (safety & tolerability) measured by blood hematology analysis in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to EOT (Week 4) and Week 8

    Hematology analysis includes: Hematocrit (Hct), Hemoglobin (Hgb), Mean Corpuscular Hemoglobin (MCH), Mean Corpuscular Hemoglobin Concentration (MCHC), Mean Corpuscular Volume (MCV), platelet count, Red Blood Cell (RBC) count, White Blood Cell (WBC) count with differential.

  4. Change in clinical laboratory parameters (safety & tolerability) measured by blood chemistry analysis in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to EOT (Week 4) and Week 8

    Clinical chemistry analysis includes: Alanine Aminotransferase (ALT), Albumin (ALB), Alkaline Phosphatase (ALK-P), Aspartate Aminotransferase (AST), bilirubin, Gamma-Glutamyl Transferase (GGT), creatinine, estimated Glomerular Filtration Rate (eGFR), C-Reactive Protein (CRP), electrolytes.

  5. Change in clinical laboratory parameters (safety & tolerability) measured by urinalysis in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to EOT (Week 4) and Week 8

    Urinalysis includes: blood, glucose, ketones, leukocyte esterase, nitrite, pH, protein and specific gravity.

Secondary outcomes

  1. Evaluate capacity for anti-viral innate immune response by measuring change in stimulated type I and type III interferon production in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to EOT (Week 4)

    Type I and type III interferon production measured using RBM Myriad's Toll-like Receptor 7/8 agonist (TLR7/8) (Resiquimod R848) TruCulture Tube assay.

  2. Difference in incidence of all-cause respiratory tract infections assessed by medical record review in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to Week 26

    Respiratory tract infections identified using revised McGeer Criteria and/or as determined by participants' medical providers.

  3. Difference in incidence of all-cause respiratory tract infections assessed by patient reported outcomes (PROs) in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to Week 26

    Respiratory tract infections identified using revised McGeer Criteria and/or as determined by participants' medical providers

  4. Difference in severity of all-cause respiratory tract infections assessed by medical record review in participants treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to Week 26

    Severity of all-cause respiratory tract infections measured using World Health Organization (WHO) 8-point ordinal scale for respiratory viral infections [minimum score 0 (uninfected) to maximum score 8 (death)] and Pneumonia Severity Index (PORT Score) (minimum: Class I, 0.1% mortality to maximum: Class V, 27% mortality) for respiratory bacterial infections. [Note: if source of infection is unknown, both WHO 8-point ordinal scale and PORT score will be collected.]

  5. Difference in severity of all-cause respiratory tract infections assessed by PROs in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Severity of all-cause respiratory tract infections measured using World Health Organization (WHO) 8-point ordinal scale for respiratory viral infections and Pneumonia Severity Index (PORT Score) for respiratory bacterial infections. [Note: if source of infection is unknown, both WHO 8-point ordinal scale and PORT score will be collected.]

  6. Difference in symptom duration of all-cause respiratory tract infections assessed by medical record review in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Symptom duration assessed by medical record review

  7. Difference in symptom duration of all-cause respiratory tract infections assessed by PROs in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Symptom duration assessed by PROs

  8. Number of courses of antibiotic/antiviral drugs prescribed for respiratory infections assessed by medical record review in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Number of courses of antibiotic/antiviral drugs assessed by medical record review

  9. Number of courses of antibiotic/antiviral drugs prescribed for respiratory infections assessed by PROs in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Number of courses of antibiotic/antiviral drugs assessed by PROs

  10. Difference in incidence of all-cause non-respiratory infection assessed by medical record review in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    All-cause non-respiratory infection identified using revised McGeer Criteria and/or as determined by participants' medical providers

  11. Difference in incidence of all-cause non-respiratory infection assessed by PROs in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    All-cause non-respiratory infection identified using revised McGeer Criteria and/or as determined by participants' medical providers

  12. Difference in severity of all-cause non-respiratory infection assessed by medical record review in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Severity of all-cause non-respiratory infection assessed by medical record review

  13. Difference in severity of all-cause non-respiratory infection assessed by PROs in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Severity of all-cause non-respiratory infection assessed by PROs

  14. Difference in severity of all-cause non-respiratory infection assessed by hospitalizations due to non-respiratory infections in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Severity of all-cause non-respiratory infection assessed by hospitalizations due to non-respiratory infections

  15. Difference in severity of all-cause non-respiratory infection assessed by mortality due to non-respiratory infections in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Severity of all-cause non-respiratory infection assessed by mortality due to non-respiratory infections

  16. Difference in symptom duration of all-cause non-respiratory infection assessed via medical record review in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Symptom duration assessed via medical record review

  17. Difference in symptom duration of all-cause non-respiratory infection assessed by PROs in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Symptom duration assessed by PROs

  18. Number of courses of antibiotic/antiviral drugs prescribed for non-respiratory infections assessed by medical record review in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    assessed by medical record review

  19. Number of courses of antibiotic/antiviral drugs prescribed for non-respiratory infections assessed by PROs in participants treated to QBKPN SSI compared to placebo

    Time frame: Baseline to Week 26

    Number of courses of antibiotic/antiviral drugs assessed by PROs

  20. Change in quality of life as measured by Dementia Quality of Life (DEMQOL) Scale in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 & 26

    Quality of life measured using DEMQOL Scale. Scores are from 28 to 112; higher scores indicate better quality of life

  21. Change in frailty as measured by the Rockwood Clinical Frailty Scale in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 & 26

    Frailty measured using Rockwood Clinical Frailty Scale. Scores are from minimum of 1 (very fit) to maximum of 7 (severely frail)

  22. Change in end-of-life prediction score as measured by Changes in Health, End-Stage Disease and Signs and Symptoms (CHESS) scale in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 & 26

    End-of-life prediction score measuring using CHESS scale. Scores are from minimum 0 (no health instability) to 5 (very high health instability)

  23. Change in all-cause mortality in participants treated with QBKPN SSI compared to placebo

    Time frame: Up to 26 weeks after first dose of study drug

    Recording all-cause mortality

Other outcomes

  1. Change in additional measures of plasma immune biomarkers that regulate innate & adaptive immune function augmentation measured using TruCulture Tube® assay (under stimulated & unstimulated conditions) of 48 analytes (cytokines & chemokines)

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 and 26

    Plasma immune biomarkers measured using TruCulture Tube assay (under stimulated and unstimulated conditions) of 48 analytes (cytokines & chemokines) using multiplex technology assessment

  2. Evaluation of duration of adaptive immune response to SARS-CoV-2 vaccination and/or infection measured by change in Cluster of Differentiation 4+ (CD4+) and Cluster of Differentiation 8+ (CD8+) T-cell response to SARS-CoV-2 S protein-derived peptides

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 and 26

    Adaptive immune response measured by CD4+ and CD8+ T-cell response to SARS-CoV-2 S protein-derived peptides

  3. Evaluation of duration of adaptive immune response to SARS-CoV-2 vaccination and/or infection measured by change in SARS-CoV-2 anti-S antibody titer in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 and 26

    Adaptive immune response to SARS-CoV-2 vaccination and/or infection measured by SARS-CoV-2 anti-S antibody titer

  4. Evaluation of duration of adaptive immune response to SARS-CoV-2 vaccination and/or infection measured by change in SARS-CoV-2 anti-S antibody secretion from antigen stimulated Peripheral Blood Mononuclear Cells (PBMCs)

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 and 26

    Adaptive immune response to SARS-CoV-2 vaccination and/or infection measured by SARS-CoV-2 anti-S antibody secretion from antigen stimulated Peripheral Blood Mononuclear Cells (PBMCs) in participants treated with QBKPN versus placebo

  5. Change in plasma metabolome measured using mass spectrometry (untargeted) to assess which metabolites are significantly changed by treatment and which may predict response to treatment in patients treated with QBKPN SSI compared to placebo.

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 and 26

    Change in plasma metabolome measured using untargeted mass spectrometry

  6. Assessment of correlation of Immunoglobulin G (IgG) antibodies to K.variicola with the NK cell function and innate immune training in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to EOT (Week 4) and Week 26

    Correlation assessed by quantification of IgG antibodies to K. variicola and correlation with NK Vue assay and RBM Myriad's TLR4 ligand (LPS) TruCulture Tube assay results

  7. Evaluation of durability of QBKPN SSI beyond EOT in participants treated with QBKPN SSI compared to placebo

    Time frame: Up to 26 weeks after first dose of study drug

    Durability of QBKPN SSI assessed by measuring innate immune training (see Outcome #1), anti-viral innate immunity (see Outcome #6), circulating Natural Killer (NK) cell function (see Outcome #37), all-cause respiratory and non-respiratory infections (see Outcomes #7 to #24)

  8. Assessment of glycemic control through hemoglobin A1C (HbA1c) in participants treated with QBKPN compared to placebo

    Time frame: Baseline to EOT (Week 4) and Weeks 8, 12 & 26.

    Change in HbA1c

  9. Assessment of NK cell function in participants treated with QBKPN SSI compared to placebo

    Time frame: Baseline to EOT (Week 4)

    NK cell function assessed by measuring stimulated IFN-y production using the NK Vue assay

Study contacts

Contact information is provided by the study sponsor or research team.

Hal Gunn, MD

CONTACT

[email protected]

604-734-1450

Oksana Korolova, Director, Clinical Operations

CONTACT

[email protected]

236-512-3119

Sponsors and collaborators

Lead sponsor

Qu Biologics Inc.

Industry

Collaborators

  • The National Research Council of Canada Industrial Research Assistance Program

Registry information

Official study title

Assessment of QBKPN Site-Specific Immunomodulator (SSI) Efficacy in Improving Innate Immune Function and Reducing All-Cause Respiratory Tract Infection Morbidity in Adults 65 Years of Age or Older Residing in the Community, in Independent-Living, Assisted-Living and Long-term Care Facilities

Acronym: RESILIENCE

Important dates

Study start
2023
Primary completion
2025
Study completion
2026
First posted
Jun 16, 2022
Registry last updated
Jan 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.