Safety, Immunogenicity and Efficacy of the Blood-stage Plasmodium Vivax Malaria Vaccine Candidate PvDBPII in Matrix M1

Exclusion Criteria

• •History of clinical malaria (any species).
• •Travel to a clearly malaria endemic locality during the study period or within the preceding six months.
• •Use of systemic antibiotics with known antimalarial activity within 30 days of CHMI (e.g. trimethoprim-sulfamethoxazole, doxycycline, tetracycline, clindamycin, erythromycin, fluoroquinolones and azithromycin).
• •Use of anti-malarials within 30 days of CHMI
• •Weight less than 50kg, as measured at the screening visit
• •Receipt of immunoglobulins within the three months prior to planned administration of the vaccine candidate.
• •Receipt of blood products (e.g., blood transfusion) at any time in the past.
• •Peripheral venous access unlikely to allow twice daily blood testing (as determined by the Investigator).
• •Receipt of an investigational product in the 30 days preceding enrolment, or planned receipt during the study period.
• •Receipt of any vaccine in the 30 days preceding enrolment, or planned receipt of any other vaccine within 30 days preceding or following each study vaccination, with the exception of licensed COVID-19 vaccines, which should not be received between 14 days before to 7 days after any study vaccination
• •Planned receipt of a COVID-19 vaccine between 2 weeks before the day of CHMI until completion of antimalarial treatment
• •Concurrent involvement in another clinical trial or planned involvement during the study period
• •Prior receipt of an investigational vaccine likely to impact on interpretation of the trial data or the P. vivax parasite as assessed by the Investigator.
• •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).
• •History of allergic disease or reactions likely to be exacerbated by any component of the vaccine e.g. egg products, Kathon
• •History of allergic disease or reactions likely to be exacerbated by malaria infection.
• •History of clinically significant contact dermatitis
• •Any history of anaphylaxis in reaction to vaccinations
• •Pregnancy, lactation or intention to become pregnant during the study.
• •Use of medications known to cause prolongation of the QT interval and existing contraindication to the use of Malarone.
• •Use of medications known to have a potentially clinically significant interaction with Riamet and Malarone.
• •Any clinical condition known to prolong the QT interval.
• •History of cardiac arrhythmia, including clinically relevant bradycardia.
• •Disturbances of electrolyte balance, e.g. hypokalaemia or hypomagnesaemia.
• •Family history of congenital QT prolongation or sudden death.
• •Contraindications to the use of both of the proposed anti-malarial medications; Riamet Malarone.
• •History of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ).
• •History of serious psychiatric condition that may affect participation in the study.
• •Any other serious chronic illness requiring hospital specialist supervision.
• •Suspected or known current alcohol abuse as defined by an alcohol intake of greater than 25 standard UK units every week.
• •Suspected or known injecting drug abuse in the 5 years preceding enrolment.
• •Hepatitis B surface antigen (HBsAg) detected in serum.
• •Seropositive for hepatitis C virus (antibodies to HCV) at screening or (unless has taken part in a prior hepatitis C vaccine study with confirmed negative HCV antibodies prior to participation in that study, and negative HCV RNA PCR at screening for this study).
• •Positive family history in both 1st AND 2nd degree relatives \< 50 years old for cardiac disease.
• •Volunteers unable to be closely followed for social, geographic or psychological reasons.
• •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.
• •Inability of the study team to contact the volunteer's GP to confirm medical history and safety to participate
• •The following constitute absolute contraindications to CHMI:
• •Acute disease, defined as moderate or severe illness with or without fever
• •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.
• •Pregnancy