PACE-CLL: Passive Antibodies Against COVID-19 With EVUSHELD in Vaccine Non-responsive CLL
Study Details
Study Description
Brief Summary
Chronic lymphocytic leukaemia (CLL) is a common lymphoid malignancy affecting older adults. CLL patients are immunocompromised by the disease itself and by several of its therapies. It has now been shown that many CLL patients do not mount an antibody response following COVID-19 vaccination and are therefore at risk of COVID-19 infection. Furthermore, patients with hematologic malignancies are known to be at increased risk of severe infection if they do acquire COVID-19 infection.
The purpose of this trial is to document evidence of passive immunity to COVID-19 infection after EVUSHELD administration with serologic and neutralization assays at multiple post administration time points in patients with no response to standard of care vaccination to COVID-19.
This trial will include a single dose of EVUSHELD to be administered, with a 1-year follow-up period, comprising of 8 health status visits.
Blood samples will be taken at screening, baseline and at multiple health status visits over the course of the year for various antibody testing and analysis. T cell reactivity to COVID-19 epitopes will be studied at baseline and again monthly for 3 months in any participants that become infected with COVID-19.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: EVUSHELD
|
Biological: EVUSHELD
EVUSHELD is a combination of 2 monoclonal antibodies (mAbs), Tixagevimab and Cilgavimab. The single dose, is to be administered intramuscular, each mAb sequentially into the deltoid
|
Outcome Measures
Primary Outcome Measures
- Passive Immunity [12 months]
The primary study objective is to confer passive immunity to CLL patients, so the primary outcome measurement is the proportion of of participants after EVUSHELD administration with anti-spike antibodies above the minimal level set as a standard for convalescent serum or 210 u/ml using the Roche assay
Secondary Outcome Measures
- Surrogate Viral Neutralization Assay [12 months]
Serum neutralization using a surrogate viral neutralization assay levels (representing levels of EVUSHELD) at months 1-6, 9 and 12 to document longevity of protection following one-time administration of the product.
- Pseudo- Viral Naturalization Assay [12 months]
Serum neutralization with a pseudo-typed viral-like particle (pseudo-virus) neutralization assay will be completed using samples obtained from 50% of participants (i.e. 25) within each treatment group at baseline and five post treatment time points. These results will be modeled over the course of the study.
- Pharmacokinetic Assessments [12 months]
Serum pharmacokinetic levels of antibodies to the COVID-19 RBD epitope at the baseline visit and visits 1, 3, 5, 7, and 8 to provide additional supportive data documenting longevity of protection following one-time administration of the product (in a subset of patients)
- COVID-19 Infection (antibodies) [12 months]
COVID-19 infection as documented by evidence of antibodies to the nucleocapsid (NC) protein
- COVID-19 Infection (RAT/PCR) [12 months]
COVID-19 infection documented by PCR or RAT.
- Symptomatic COVID-19 infection [12 months]
Symptomatic COVID-19 infection and outcomes as documented by participant clinical symptomatology and status (hospital admission, ICU admission, or death) at conclusion of the trial
- Safety of EVUSHELD [12 months]
Safety will be evaluated at each clinical visit and will include the documentation of; any changes in grade/seriousness or severity of baseline medical history, body temperature, blood pressure, oxygen saturation, heart rate, pulse, and review of symptoms, toxicities at monthly time points. Toxicities will be graded according to the NCI Common Terminology Criteria for Adverse Events, version 5.0 (NCI CTCAE, v5.0).
- Baseline T cell responses to COVID-19 as a potential predictor of breakthrough COVID-19 infections [12 months]
T cell responses at baseline will be evaluated by COVID-19-specific LEGEND-plex cytokine detection with stratification according to participant treatment group to help understand mechanisms of viral escape in participants who do become infected with COVID after EVUSHELD administration.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Have a diagnosis of CLL according to international working group CLL criteria
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Treatment-naïve, post treatment or on-treatment for CLL
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Male or female ≥ 18 years of age on day of signing informed consent
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Weight ≥ 40 kg at the screening
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Have received at least 2 standard of care SARS-CoV-2 vaccines within the last 18 months prior to enrolment. These vaccines may include all vaccines given in Canada since the beginning of the pandemic including: Pfizer BNT162b2 (COMIRNATY®), Moderna mRNA-1273 (SPIKEVAX®), and Astra Zeneca AZD1222 (Vaxzevria®)
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Last SARS-CoV-2 vaccination ≥28 days ago and no more than 18 months ago.
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Participants must have a demonstrated absent or suboptimal response to standard of care SARS-CoV-2 vaccinations on screening bloodwork and will be prioritized for this study as they are deemed to be at higher risk of serious COVID-19 infection.
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Have a performance status of 0-2 on the ECOG Performance Scale.
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Have adequate organ function laboratory values, anytime during the screening period
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Have a life expectancy > 6 months in the opinion of the referring hematologist.
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Female subject of childbearing potential should have a negative serum pregnancy test prior to receiving study medication (study day 0).
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Female participants of childbearing potential should be willing to use 2 highly effective methods of birth control or be surgically sterile, or abstain from heterosexual activity for the duration of the study (after signing consent) to prevent pregnancy. Participants of childbearing potential are those who have not been surgically sterilized or have not been free from menses for > 1 year.
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Male participants should be surgically sterile or agree to use a highly effective method of contraception for the duration of the study (after signing consent) to prevent pregnancy in their partner.
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Participants must agree to abstain from donating blood or plasma from the time of informed consent and for one year
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Able and willing to provide signed informed consent for the trial
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Ability to comply with protocol requirements.
Exclusion Criteria:
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Signs and symptoms consistent with symptomatic COVID-19 illness within 30 days of consent.
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Prior (within 30 days), current, or planned use of any of COVID-19 convalescent plasma, other monoclonal antibodies against SARS-CoV-2 or any COVID-19 treatment, or if clinically indicated as standard of care for a COVID-19 infection, should not be administered within 14 days of the EVUSHELD administration
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Current infection requiring treatment with antibiotics or antifungals (not including prophylactic medications given with current therapy). Note: Participants completing a course of antibiotics for acute infection 7 days prior to SD0 and who do not experience a recurrence of symptoms or fever are eligible.
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Has a known history of active TB (Bacillus Tuberculosis)
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Has known psychiatric or substance abuse disorders that would interfere with adherence with the requirements of the trial.
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Previous hypersensitivity reaction following administration of a monoclonal antibody
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Currently pregnant, lactating or breast feeding
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Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 21 days of treatment (SD0).
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Receive a COVID-19 booster shot within 90 days of EVUSHELD administration
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Known history of allergy to any component of the study drug formulation or its excipients
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History of clinically significant bleeding disorder, or prior history of significant bleeding or bruising following IV infusions or venipuncture.
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Any other significant disease, disorder, or finding that may; significantly increase the risk to the participant because of participation in the study; affect the ability of the subject to participate in the study; or impair interpretation of the study data.
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Blood drawn in excess of a total of 450 mL (1 unit) for any reason within 30 days prior to enrollment.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Sunnybrook Health Sciences Cente | Toronto | Ontario | Canada | M4N 3M5 |
Sponsors and Collaborators
- Sunnybrook Health Sciences Centre
- AstraZeneca
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 3989