Malaria, Malaria,Falciparum
Conditions
Keywords
PfSPZ Vaccine, HIV+, Plasmodium falciparum, Sporozoites
Brief summary
This is a randomized, double-blind, placebo-controlled trial to evaluate safety and tolerability of PfSPZ Vaccine administered as five doses of 9.0x10\^5 PfSPZ or normal saline at 0, +2, +4, +6 and +28 days to healthy HIV negative adult volunteers and healthy HIV positive volunteers in Tanzania.
Detailed description
This trial is a single center trial designed to assess the safety, tolerability, immunogenicity and efficacy of PfSPZ Vaccine (9.0x10\^5 PfSPZ given at 0, +2, +4, +6 and +28 days (Group 1, HIV negative, and Group 2, HIV positive)). Controls will receive parallel injections with normal saline (NS). All administrations of PfSPZ or NS will be by direct venous inoculation (DVI). Twenty-one male and female adult volunteers, aged from 18 to 45 years, who live in and around the Bagamoyo township, will be enrolled based on pre-defined inclusion and exclusion criteria. 12/21 subjects will be HIV positive volunteers (who clinical stage 1) on stable anti-retroviral therapy (ART) for at least 3 months with a CD4+ cell count above 500 cells/μL at screening. The rest (9/21) will be healthy HIV negative adults. Treatment allocation will be double-blind within Group 1 and 2b but not between the groups or subgroups. Immunizations will begin with healthy HIV negative volunteers first (Group 1), before inoculation of HIV positive volunteers (Groups 2a and 2b). Transitioning from immunization of HIV negative to immunization of HIV positive will begin by immunizing a sentinel group of 3 HIV positive individuals with a reduced vaccine dose of 4.5x10\^5 PfSPZ (Group 2a). This transition will be staggered by at least two (2) weeks, to allow for a safety data review. If the safety data do not meet pause criteria, this will signal a go for transitioning to immunizations of sentinel group of three (3) HIV positive volunteers. If pause criteria are met, there will be no immediate transition, and instead an ad-hoc meeting of the Safety Monitoring Committee (SMC) will be called for an independent review and recommendation. Transition from the unblinded HIV positive sentinel Group 2a to the full study cohort of double blinded placebo controlled HIV positive volunteers (Group 2b), will also be staggered for at least two (2) weeks. There will be a scheduled review by the SMC of safety data collected from the sentinel HIV positive group for up to 7 days after the fourth immunization. After the safety review, transition to the main HIV positive group (Group 2b) will take into account the SMC recommendation(s).
Interventions
BIOLOGICALPfSPZ Vaccine
Aseptic, purified, metabolically active, non-replicating, radiation-attenuated, cryopreserved Pf sporozoites.
OTHERNormal Saline Placebo
0.9% sodium chloride solution
BIOLOGICALPfSPZ Challenge
Aseptic, purified, live, infectious, cryopreserved Pf sporozoites.
Sponsors
Ifakara Health Institute
Swiss Tropical & Public Health Institute
Medical Care Development, Inc.
Sanaria Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Male and female adults, from 18 to 45 years of age * Long term (at least two years) or permanent residence in the Bagamoyo district or nearby districts in Coastal and Dar-es-Salaam regions * Availability through mobile phone 24 hours a day during the whole study period * Ability and willingness to complete the study visit schedule for safety follow-up and protocol compliance * Agreement to provide personal contact information and contact information of a third party household member or close friend to study team * Agreement not to participate in any other clinical study involving investigational medicinal products during the study period, except enrollment in observational studies (such a co-enrollment must be approved by the PI) * Agreement to release medical and other information concerning contra-indications for participation in the study, and to be attended by a study clinician for physical examination and clinical investigations including electrocardiogram (ECG) * Willingness to undergo all blood, urine and stool tests (as specified in the protocol) and additional tests that may be ordered by the study clinician to rule-out significant abnormality(ies) * Female volunteers must be willing to take measures not to become pregnant if selected for participation in the trial and to undergo serum pregnancy test at screening and at defined time-points during the trial * Volunteers for enrollment into HIV positive sub-groups must have: 1. Documented HIV infection, be in general good health and on stable ART use for at least three (3) months, preferably six (6), prior to screening 2. WHO clinical stage 1 of HIV disease 3. CD4+ T-cell count \>500 cells/μL at screening 4. Attending a care and treatment centre (CTC) within the study area for medical management of HIV infection, and agreeing to maintain regular attendance to such care and treatment centre while participating in the study 5. Agreement to allow the clinical team to contact and coordinate care with the volunteer's HIV CTC. * Correctly answering 10 out of 10 questions during informed consent process to demonstrate the understanding of study design, study procedures, risks and benefits * Signing and dating written informed consent, in accordance with local practice.
Exclusion criteria
* Previous receipt of an investigational malaria vaccine or drug in the last 5 years * Receipt of standard vaccinations within 4 weeks prior to the first immunization with a PfSPZ product or are planning to take standard vaccinations during the trial through 4 weeks following the last injection with a PfSPZ product * Participation in any other clinical trial involving investigational medicinal products within 30 days prior to the onset of the study * Clinically significant cardiac abnormalities as indicated by history, physical examination or clinically significant abnormalities in electrocardiogram (ECG) * Positive family history in a 1st or 2nd degree relative for cardiac disease at age\< 50 years old * A history of psychiatric disease * History of afebrile seizures, atypical febrile seizures or epilepsy * History of drug or alcohol abuse interfering with normal social function * History of chronic immunodeficiency condition (other than HIV) or autoimmune disease * The use of chronic immunosuppressive drugs, antibiotics, or other immune modifying drugs within three months prior to study onset (ART and inhaled and topical corticosteroids are allowed) * Meeting
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety of PfSPZ Vaccine - solicited symptoms | From day of vaccination to 7-days post vaccination. | Occurrence of solicited symptoms during a 7-day surveillance period after vaccination (day of vaccination (Vx) and +7 days post vaccination). |
| Safety of PfSPZ Vaccine - unsolicited symptoms | From day of vaccination to 28-days post vaccination. | Occurrence of unsolicited symptoms during a 28-day surveillance period after each vaccination. |
| Safety of PfSPZ Vaccine - laboratory abnormalities | Day of immunization to approximately 11 weeks after the last vaccination (approximately 36 weeks). | Occurrence of laboratory abnormalities including significant drops in CD4 T cell counts or increases in viral load. |
| Safety of PfSPZ Vaccine - serious adverse events | Day of immunization to approximately 11 weeks after the last vaccination (approximately 36 weeks). | Occurrence of serious adverse events during the study period. |
| Safety of PfSPZ Vaccine - breakthrough infection | Day of immunization to approximately 11 weeks after the last vaccination (approximately 36 weeks). | \- Occurrence of Pf infection of vaccine type detected at any point after the first vaccination (retrospectively determined). |
Countries
Tanzania
Outcome results
None listed