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Trial record 1 of 1 for:    NCT04442048
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Immunization With IMM-101 vs Observation for Prevention of Respiratory and Severe COVID-19 Related Infections in Cancer Patients at Increased Risk of Exposure (COV-IMMUNO)

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ClinicalTrials.gov Identifier: NCT04442048
Recruitment Status : Active, not recruiting
First Posted : June 22, 2020
Last Update Posted : September 13, 2022
Immodulon Therapeutics Ltd
BioCan Rx
Canadian Cancer Society (CCS)
ATGen Canada Inc
Canadian Centre for Applied Research in Cancer Control (ARCC)
Ontario Institute for Cancer Research
Information provided by (Responsible Party):
Canadian Cancer Trials Group

Brief Summary:
The purpose of this study is to find out if immunization with IMM-101 will reduce the incidence of severe respiratory and COVID-19 infections in cancer patients.

Condition or disease Intervention/treatment Phase
Cancer Covid-19 Biological: IMM-101 Other: Observation Phase 3

Detailed Description:
IMM-101 is a new type of immune stimulating therapy being developed for the treatment of cancer that may also help in preventing severe respiratory and COVID-19 infections. Laboratory tests show that IMM-101 works by activating parts of the immune system that are also involved with protecting against viral and bacterial infections, so that if you are exposed to these types of infections your body may be able fight off the infection better. That could help prevent severe symptoms from respiratory and COVID-19 related infections. It has been studied in over 300 cancer patients who have also been receiving other cancer treatments, including chemotherapy and radiation, and seems promising, but it is not clear if it can offer better results than not having the immunization at all.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 195 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: COV-IMMUNO: A Randomized, Phase III Trial of Immunization With IMM-101 Versus Observation for the Prevention of Severe Respiratory and COVID-19 Related Infections in Cancer Patients at Increased Risk of Exposure
Actual Study Start Date : June 25, 2020
Estimated Primary Completion Date : December 31, 2022
Estimated Study Completion Date : June 30, 2023

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: IMM-101
The treatment regimen with IMM-101 will be one 1.0 mg (= 0.1 mL) dose given on Day 0, followed by a second dose of 0.5 mg (= 0.05 mL) on Day 14 (-2/+5 days), and a third Dose of 0.5 mg (= 0.05 mL) on Day 45 (+/-14 days)
Biological: IMM-101
Three doses of IMM-101 on days 0, 14, and 45.

Active Comparator: Observation Other: Observation
No active treatment. Observation only

Primary Outcome Measures :
  1. The rate of "flu-like illness" which includes: [ Time Frame: 1 year ]
    • WHO definition of "influenza-like illness" (ILI) [Fitzner 2018] or confirmed viral/bacterial respiratory infection AND
    • Results in a change or delay in cancer treatment or requirement for and unscheduled medical assesment, hospitalization or death.

Secondary Outcome Measures :
  1. The incidence of documented COVID-19 infection (confirmed by any Health Canada approved COVID-19 test. Both symptomatic and asymptomatic infections will be documented [ Time Frame: 1 year ]
  2. The rate of severe respiratory and COVID-19 infection defined as a confirmed COVID-19 infection leading to hospitalization, ICU admission or death [ Time Frame: 1 year ]
  3. The number of events that meet the definition of the primary endpoint, as measured within the one-year follow-up (patients may meet the primary endpoint more than once and be counted multiple times). [ Time Frame: 1 year ]
  4. The incidence of COVID-19 seroconverted patients between baseline, 3 months, 6 months and 12 months [ Time Frame: 3, 6, and 12 months ]
  5. The incremental cost-effectiveness ratio (in the unit of CAD$ per life-years gained) measured with EQ-5D-5L [ Time Frame: 1 year ]
  6. Failure-free survival, as time from enrollment to recurrence or progression declared by the investigator on the basis of objective standard evaluation consistent with the disease site or death [ Time Frame: 1 year ]
  7. Overall survival (OS), as time from enrollment to death from any cause [ Time Frame: 1 year ]
  8. Incidence, frequency, and severity of AEs considered possibly, probably or definitely related to receipt of IMM-101 [ Time Frame: 1 year ]
  9. Incidence and frequency of local injection site reactions subsequent to IMM-101 administration [ Time Frame: 1 year ]
  10. Incidence and duration of ICU admission related to documented COVID-19 infection [ Time Frame: 1 year ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patient must be undergoing (or be planned to undergo) active treatment for one or more solid malignancy, lymphoma or myeloma. active treatment includes adjuvant, neoadjuvant and palliative intent treatment with surgery, radiation, chemotherapy, targeted therapy or immunotherapy.
  • Patients must have one or more of the following risk factors [CDC 2019] for a severe COVID-19 infection:

    • Age > 65 years old
    • Hypertension (on medications);
    • Type 1 or 2 Diabetes (on medication)
    • A relevant chronic condition as per the investigator based on the medical record, including:

      • heart (e.g. heart failure, coronary artery disease, congenital heart disease, cardiomyopathies, and pulmonary hypertension)
      • lung (e.g. chronic obstructive pulmonary disease (COPD including emphysema and chronic bronchitis), moderate to severe asthma, idiopathic pulmonary fibrosis and cystic fibrosis)
      • liver cirrhosis
      • serious kidney disease requiring dialysis
    • Receiving systemic therapy (such as cytotoxic chemotherapy, immunotherapy or targeted agents excluding single-agent hormonal therapy)
    • Body Mass Index > 40
    • Living in a nursing home or long term care facility
  • Patient must have a life expectancy of >6 months as assessed by the investigator
  • Patient must have an ECOG Performance Status ≤ 2
  • Patient has adequate organ function appropriate for the therapy the patient is planned to receive in the opinion of the investigator and based on local assessment and practices.
  • Patient is aged ≥ 18 years
  • Patient has agreed to receive pneumococcal vaccination and a seasonal influenza vaccination in accordance with Canadian Guidelines.
  • Patient is able (i.e. sufficiently fluent) and willing to complete the health utility questionnaires in either English or French.
  • Patient consent must be appropriately obtained in accordance with applicable local and regulatory requirements. Each patient must sign a consent form prior to enrollment in the trial to document their willingness to participate.
  • Patient must be willing to provide identifying information including provincial health insurance number to facilitate data linkage and follow up.
  • Patients must be accessible for treatment and follow-up. Investigators must assure themselves the patients enrolled on this trial will be available for complete documentation of the treatment, adverse events, and follow-up.
  • Women/men of childbearing potential must have agreed to use a highly effective contraceptive method throughout the treatment period and for at least 3 months after discontinuation of treatment.

Exclusion Criteria:

  • Patient previously received treatment with IMM-101.
  • Patient cannot have either at present or in the past, a positive test for COVID-19 infection. If a patient has been tested for COVID-19, result must be confirmed as negative prior to enrollment.
  • Patient cannot have experienced "flu-like symptoms" within 14 days prior to enrollment, including fever, extreme fatigue, new or worsening cough, myalgias, new or worsening dyspnea, and/or sputum production.
  • Patient is receiving concomitant treatment with another investigational product or has received such treatment within the 3 weeks prior to enrollment.
  • Patient has any co-existing active infection that, in the opinion of the Investigator, may increase the risk associated with study participation or study drug administration, impair the ability of the subject to receive protocol therapy, interfere with the patient's participation for the full duration of the study, or is not in the best interest of the patient to participate.
  • Patient has previously experienced an allergic reaction to any mycobacterial product, including the BCG vaccine.
  • Patients with superficial bladder cancer or any other condition currently receiving or planned to be treated with BCG.
  • Patient has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies) or a known history of or is known to have a positive test for Hepatitis B (HBsAg reactive) or Hepatitis C (HCV RNA [qualitative]).
  • Patients with prior or concurrent leukemia.
  • Patient has had a prior bone marrow transplant.
  • Patient is pregnant or breast-feeding
  • Patient has documented history of clinically severe autoimmune disease or a syndrome that requires systemic steroids or immunosuppressive agents. This includes patient requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent, or depot corticosteroids in the 6 weeks before enrollment) or immunosuppressant drugs (such as azathioprine, tacrolimus, cyclosporine, etc.) within the 14 days prior to enrollment. Inhaled or topical steroids, and adrenal replacement steroid doses ≤ 10 mg daily prednisone equivalent, are permitted in the absence of active autoimmune disease. Steroids used for premedication prior to chemotherapy or as part of a chemotherapy regimen are allowed.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04442048

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Canada, Ontario
Juravinski Cancer Centre at Hamilton Health Sciences
Hamilton, Ontario, Canada, L8V 5C2
London Regional Cancer Program
London, Ontario, Canada, N6A 5W9
Ottawa Hospital Research Institute
Ottawa, Ontario, Canada, K1H 8L6
Odette Cancer Centre
Toronto, Ontario, Canada, M4N 3M5
University Health Network
Toronto, Ontario, Canada, M5G 2M9
Canada, Quebec
CHUM-Centre Hospitalier de l'Universite de Montreal
Montreal, Quebec, Canada, H2X 3E4
The Research Institute of the McGill University
Montreal, Quebec, Canada, H4A 3J1
CIUSSS de l'Estrie - Centre hospitalier
Sherbrooke, Quebec, Canada, J1H 5N4
Sponsors and Collaborators
Canadian Cancer Trials Group
Immodulon Therapeutics Ltd
BioCan Rx
Canadian Cancer Society (CCS)
ATGen Canada Inc
Canadian Centre for Applied Research in Cancer Control (ARCC)
Ontario Institute for Cancer Research
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Study Chair: Rebecca A Auer Ottawa Hospital Research Institute
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Responsible Party: Canadian Cancer Trials Group
ClinicalTrials.gov Identifier: NCT04442048    
Other Study ID Numbers: IC8
First Posted: June 22, 2020    Key Record Dates
Last Update Posted: September 13, 2022
Last Verified: June 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Respiratory Tract Infections
Pneumonia, Viral
Virus Diseases
Coronavirus Infections
Coronaviridae Infections
Nidovirales Infections
RNA Virus Infections
Lung Diseases
Respiratory Tract Diseases