Safety and Immunogenicity of Pvs25-IMX313/Matrix-M1 Vaccine
Study Details
Study Description
Brief Summary
This is an open-label, single-centre, non-randomised, first-in-human Phase Ia study to assess the safety and immunogenicity of the Pvs25-IMX313 vaccine, administered in Matrix-M1 adjuvant.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Early Phase 1 |
Detailed Description
Volunteers will be recruited into one of three groups (n=8-10 per group) at the Centre for Clinical Vaccinology and Tropical Medicine (CCVTM), Oxford over approximately 18 months. All volunteers will receive three doses of Pvs25-IMX313 in Matrix-M1, administered intramuscularly and given four weeks apart. Enrolment will be staggered with clinical and safety reviews, follow-up visits and monitoring via a diary card.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Group 1 (low dose) 8-10 volunteers receiving three doses of 10 µg Pvs25-IMX313 in 50 µg Matrix-M1 on days 0, 28 and 56 via intramuscular injection (IM) in the deltoid region of the arm |
Biological: Pvs25-IMX313/Matrix-M1
Three doses of Pvs25-IMX313 in Matrix-M1 at different concentrations
|
| Experimental: Group 2 (standard dose) 8-10 volunteers receiving three doses of 50 µg Pvs25-IMX313 in 50 µg Matrix-M1 on days 0, 28 and 56 via intramuscular injection (IM) in the deltoid region of the arm |
Biological: Pvs25-IMX313/Matrix-M1
Three doses of Pvs25-IMX313 in Matrix-M1 at different concentrations
|
| Experimental: Group 3 (fractional dose) 8-10 volunteers receiving two doses of 50 µg Pvs25-IMX313 in 50 µg Matrix-M1 on days 0 and 28, followed by one dose of 10 µg Pvs25-IMX313 in 50 µg Matrix-M1 on day 56 via intramuscular injection (IM) in the deltoid region of the arm |
Biological: Pvs25-IMX313/Matrix-M1
Three doses of Pvs25-IMX313 in Matrix-M1 at different concentrations
|
Outcome Measures
Primary Outcome Measures
- To assess safety and tolerability of the Pvs25-IMX313/Matrix-M1 vaccine in healthy adult volunteers by assessing occurrence of solicited local reactogenicity signs and symptoms in the 7 days following each vaccination using the patient-reported e-diaries [7 days following each vaccination]
Occurrence of solicited local reactogenicity signs and symptoms using the patient-reported e-diaries
- To assess safety and tolerability of the Pvs25-IMX313/Matrix-M1 vaccine in healthy adult volunteers by assessing occurrence of solicited systemic reactogenicity signs and symptoms in the 7 days following each vaccination using patient-reported e-diaries [7 days following each vaccination]
Occurrence of solicited systemic reactogenicity signs and symptoms using the patient-reported e-diaries
- Safety and tolerability of the Pvs25-IMX313/Matrix-M1 vaccine in healthy adult volunteers, assessed through collection of data on the frequency, duration and severity of solicited and unsolicited adverse events. [28 days following the vaccination]
The specific endpoints for safety and tolerability will be actively and passively collected data on adverse event
- Safety of the Pvs25-IMX313/Matrix-M1 vaccine in healthy adult volunteers, assessed through the number of participants with abnormal laboratory test results [28 days following vaccination]
Occurrence of change from baseline laboratory test results
- Assessment of the safety and tolerability of the Pvs25-IMx313/Matrix-M1 vaccine in healthy adult volunteers assessed through the number of participants with serious adverse events [Whole duration of the study period (8 months following enrolment)]
Occurrence of serious adverse events including grading of causality
Secondary Outcome Measures
- Assessment of the humoral immunogenicity of the Pvs25-IMX313/Matric-M1 vaccine, when administered to healthy adult volunteers as assessed by humoral responses to the Pvs25 protein [Days 1, 29, 57, 140 and 240.]
Antibody responses to the Pvs25 protein will be assessed through total IgG isotypes and avidity
- Assessment of the cellular immunogenicity of the Pvs25-IMX313/Matrix-M1 vaccine, when administered to healthy adult volunteers as assessed by cellular responses to the Pvs25 protein. [Days 1, 29, 57, 140 and 240.]
T cell responses to Pvs25 will be assessed by ex vivo enzyme-linked immunospot assays (ELISpot) and flow cytometry assays.
- Assessment of ex vivo efficacy of the Pvs25-IMX313/Matrix-M1 vaccine when administered to healthy adult volunteers using direct membrane feeding assays as assessed by transmission-reducing activity. [Days 1, 29, 57, 140 and 240.]
Transmission-reducing activity
- Assessment of ex vivo efficacy of the Pvs25-IMX313/Matrix-M1 vaccine when administered to healthy adult volunteers using direct membrane feeding assays as assessed by transmission-blocking activity. [Days 1, 29, 57, 140 and 240.]
Transmission-blocking activity
Eligibility Criteria
Criteria
Inclusion Criteria:
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Healthy adult aged 18 to 45 years.
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Able and willing (in the Investigator's opinion) to comply with all study requirements.
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Willing to allow the Investigators to discuss the volunteer's medical history with their GP.
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Women only: must practice continuous effective contraception for the duration of the study. This includes established use of oral, injected or implanted hormonal methods of contraception, placement of an intrauterine device or intrauterine system, total abdominal hysterectomy, male sterilisation if the vasectomised partner is the sole partner for the participant, true abstinence, when this is in line with the preferred and usual lifestyle of the participant (periodic abstinence and withdrawal are not acceptable methods of contraception).
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Agreement to refrain from blood donation for the duration of the study.
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Able and willing to provide written informed consent to participate in the trial.
Exclusion Criteria:
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History of clinical malaria (any species).
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Travel to a clearly malaria endemic locality during the study period or within the preceding six months.
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Use of immunoglobulins or blood products (e.g., blood transfusion) in the last three months.
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Receipt of any vaccine in the 30 days preceding enrolment, or planned receipt of any other vaccine within 30 days following each study vaccination, with the exception of --COVID-19 vaccines, which should not be received between 14 days before to 7 days after any study vaccination.
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Receipt of an investigational product in the 30 days preceding enrolment, or planned receipt during the study period.
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Concurrent involvement in another clinical trial or planned involvement during the study period.
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Prior receipt of an investigational vaccine likely to impact on interpretation of the trial data, as assessed by the Investigator.
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Any confirmed or suspected immunosuppressive or immunodeficient state, including HIV infection; asplenia; recurrent, severe infections and chronic (more than 14 days) immunosuppressant medication within the past 6 months (inhaled and topical steroids are allowed).
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History of allergic disease or reactions likely to be exacerbated by any component of the -vaccine.
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Any history of anaphylaxis in reaction to vaccinations.
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Pregnancy, lactation or intention to become pregnant during the study.
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History of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ).
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History of serious psychiatric condition that may affect participation in the study.
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Any other serious chronic illness requiring hospital specialist supervision.
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Suspected or known current alcohol abuse as defined by an alcohol intake of greater than 25 standard UK units every week.
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Suspected or known injecting drug abuse in the 5 years preceding enrolment.
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Hepatitis B surface antigen (HBsAg) detected in serum.
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Seropositive for hepatitis C virus (antibodies to HCV) at screening (unless volunteer has taken part in a prior hepatitis C vaccine study with confirmed negative HCV antibodies prior to participation in that study, and negative HCV ribonucleic acid (RNA) PCR at screening for this study).
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Volunteers unable to be closely followed for social, geographic or psychological reasons.
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Any clinically significant abnormal finding on biochemistry or haematology blood tests, urinalysis or clinical examination. In the event of abnormal test results, confirmatory repeat tests will be requested. Procedures for identifying laboratory values meeting exclusion criteria are shown in SOP VC027.
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Any other significant disease, disorder, or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data.
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Inability of the study team to contact the volunteer's GP to confirm medical history and safety to participate.
Vaccination and re-vaccination exclusion criteria:
Absolute CI's:
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Anaphylactic reaction following administration of vaccine
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Pregnancy
CI's at that point in time (may be rescheduled):
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Acute disease (moderate/severe illness with or without fever)
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T>37.5C
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Current COVID-19 infection, defined as ongoing symptoms with positive COVID-19 PCR swab test taken during current illness or positive COVID-19 PCR swab test within preceding 14 days without symptoms. Vaccinations will be delayed by a minimum of 2 weeks from the date of the first positive COVID-19 PCR swab, as long as symptoms are improving or resolved. It will be at the discretion of the Investigator to withdraw a participant if they develop severe COVID-19 disease.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | CCVTM, University of Oxford, Churchill Hospital | Oxford | United Kingdom | OX3 7LE |
Sponsors and Collaborators
- University of Oxford
Investigators
- Principal Investigator: Angela M Minassian, DPhil FRCP, Centre for Clinical Vaccinology and Tropical Medicine, Churchill Hospital, Oxford, United
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- VAC084