Safety, Tolerability and Efficacy of PfSPZ Vaccine in Healthy Children and Infants 5 Months - 9 Years Living in Kenya

NCT ID: NCT02687373

Last Updated: 2019-04-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1/PHASE2

Total Enrollment

337 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-07-21

Study Completion Date

2018-08-14

Brief Summary

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This study will be conducted in Siaya County in Nyanza Province, western Kenya. Healthy children aged 5 months through 9 years of age living within approximately 10 km of the study clinic(s) (Siaya County Referral Hospital, or Wagai dispensary, a government health facility in Wagai division) will be eligible for participation in Part 1; healthy infants aged 5 months - 12 months inclusive will be eligible for Part 2.

Detailed Description

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Part 1: Age De-Escalation and Dose Escalation Part 1 of this trial is a randomized blinded evaluation of the safety and tolerability of PfSPZ Vaccine administered by DVI in healthy children and infants living in an area of high malaria transmission. A maximum of 156 children from 5 months to 9 years inclusive at vaccination will be enrolled and randomized to receive vaccine or normal saline (NS) placebo by DVI. Total participation time in the dose escalation trial ranges from 5-16 weeks per participant from screening visit to close out or 4 - 12 weeks from enrolment to close out.

Vaccination will begin in the 5-9 year age group at a dosage of 4.5 x10\^5 PfSPZ. A single vaccination will be administered by DVI to each of 12 participants aged 5-9 years (inclusive) of age, 8 receiving PfSPZ vaccine and 4 participants receiving NS placebo by DVI, with treatment allocation randomized and double-blind. Once the initial dose has been shown to be well tolerated and without safety concerns, the next higher dose of 9.0 x 10\^5 PfSPZ will be administered to a second group of 5-9 year olds. Once this has been shown to be well tolerated and without safety concerns, the highest dose of 1.8 x 10\^6 PfSPZ will be given to a third group of 5-9 year olds and concurrently the lowest dose (1.35 x10\^5) will be given to a same-sized group of younger children aged 13-59 months. Two weeks later, this dose will be escalated to 2.7 x10\^5 PfSPZ in a second group of children aged 13-59 months. Only once this dose is shown to be well-tolerated and without safety concerns will PfSPZ Vaccine, at the lowest dose, be given to infants aged 5 - 12 months. Within each age group, dosages will increase stepwise until they reach 1.8 x 10\^6 PfSPZ, with the initiation of each group staggered by at least 2 weeks, provided that no safety thresholds are surpassed. In each dosage level, the PfSPZ Vaccine or placebo will be provided to a limited number of participants each day (e.g. 3 participants from one age group on days 1 through 4). The PfSPZ Vaccine dose will only be increased to the next dose level when safety has been assessed in subjects of the first group. The same procedures will be followed for all doses. Children in all age groups who are enrolled to receive the 2 highest doses, i.e. 9.0 x 10\^5 or 1.8 x 10\^6 PfSPZ, or placebo, will receive a second vaccination of the same dose after 8 weeks, provided the first vaccination at this dose level did not show safety signals.

Part 2: Safety and Efficacy Part of this study will be conducted in the outpatient areas of Siaya County Referral Hospital, a large referral hospital in western Kenya and in Wagai dispensary. A maximum of 416 infants from 5 M to 12 M inclusive at vaccination will be enrolled into this safety and efficacy trial and randomized to receive PfSPZ Vaccine at a dose determined during Part 1 of the trial (dose escalation), but likely to be 4.5x10\^5, 9.0 x10\^5and 1.8 x 10\^6 administered x 3 doses ; and NS placebo administered x 3 doses, all by DVI administered at 8 week intervals.

Participants (N = 416, with 104 in each study arm) will be randomly assigned in a double blinded fashion to receive one of the following PfSPZ Vaccine regimes:

Group 1 (N=104): The highest dose that is determined to be safe and well tolerated in the Part 1 trial, administered in 3 doses by DVI at 0, 8 and 16 weeks. Likely dosage will be 1.8 x 10\^6 PfSPZ per dose.

Group 2 (N=104): The second highest dose, which is half of the highest dose, administered in 3 doses by DVI at 0, 8 and 16 weeks. Likely dosage will be 9.0 x 10\^5 PfSPZ per dose.

Group 3 (N=104): A lower dose (half of the second highest dose) administered in 3 doses by DVI at 0, 8, 16 weeks. Likely dosage will be 4.5x 10\^5 PfSPZ per dose.

Group 4 (N=104): A placebo arm, will receive NS by DVI, 3 times at 8 week intervals.

Conditions

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Malaria

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Part 1: Grp 1A - PfSPZ Vaccine

Children aged 5-9 years (inclusive) of age will be enrolled in this group.

N=8; Dose of 4.5 x 10\^5 PfSPZ Vaccine administered DVI, as a single vaccination.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 1A - Normal Saline

Children aged 5-9 years (inclusive) of age will be enrolled in this group.

N=4; Normal saline administered DVI, as a single vaccination.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 1B - PfSPZ Vaccine

Children aged 5-9 years (inclusive) of age will be enrolled in this group.

N=8; Two doses of 9.0 x 10\^5 PfSPZ Vaccine administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 1A dose has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 1B - Normal Saline

Children aged 5-9 years (inclusive) of age will be enrolled in this group.

N=4; Two doses of normal saline administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 1A dose has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 1C - PfSPZ Vaccine

Children aged 5-9 years (inclusive) of age will be enrolled in this group.

N=8; Two doses of 1.8 x 10\^6 PfSPZ Vaccine administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after the 1st dose of Grp 1B has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 1C - Normal Saline

Children aged 5-9 years (inclusive) of age will be enrolled in this group.

N=4; Two doses of normal saline administered DVI, 8 weeks apart. The 1st dose will be administered after the 1st dose of Grp 1B has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 2A - PfSPZ Vaccine

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=8; Dose of 1.35 x 10\^5 PfSPZ Vaccine administered DVI, as a single vaccination. This dose will be administered 2 weeks after the 1st dose of Grp 1B has been shown to be well-tolerated and without safety concerns.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 2A - Normal Saline

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=4; Normal saline administered DVI, as a single vaccination. This dose will be administered 2 weeks after the 1st dose of Grp 1B has been shown to be well-tolerated and without safety concerns.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 2B - PfSPZ Vaccine

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=8; Dose of 2.7 x 10\^5 PfSPZ Vaccine administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 2A has been shown to be well-tolerated and without safety concerns.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 2B - Normal Saline

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=4; Normal saline administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 2A has been shown to be well-tolerated and without safety concerns.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 2C - PfSPZ Vaccine

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=8; Dose of 4.5 x 10\^5 PfSPZ Vaccine administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 2B has been shown to be well-tolerated and without safety concerns.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 2C - Normal Saline

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=4; Normal saline administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 2B has been shown to be well-tolerated and without safety concerns.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 2D - PfSPZ Vaccine

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=8; Two doses of 9.0 x 10\^5 PfSPZ Vaccine administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 2C has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 2D - Normal Saline

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=4; Two doses of normal saline administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 2C has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 2E - PfSPZ Vaccine

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=8; Two doses of 1.8 x 10\^6 PfSPZ Vaccine administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 2D has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 2E - Normal Saline

Children aged 13-59 months (inclusive) of age will be enrolled in this group.

N=4; Two doses of normal saline administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 2D has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 3A - PfSPZ Vaccine

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=8; Dose of 1.35 x 10\^5 PfSPZ Vaccine administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 2B has been shown to be well-tolerated and without safety concerns.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 3A - Normal Saline

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=4; Normal saline administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 2B has been shown to be well-tolerated and without safety concerns.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 3B - PfSPZ Vaccine

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=8; Dose of 2.7 x 10\^5 PfSPZ Vaccine administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 3A has been shown to be well-tolerated and without safety concerns.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 3B - Normal Saline

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=4; Normal saline administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 3A has been shown to be well-tolerated and without safety concerns.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 3C - PfSPZ Vaccine

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=8; Dose of 4.5 x 10\^5 PfSPZ Vaccine administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 3B has been shown to be well-tolerated and without safety concerns.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 3C - Normal Saline

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=4; Normal saline administered DVI, as a single vaccination. This dose will be administered 2 weeks after Grp 3B has been shown to be well-tolerated and without safety concerns.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 3D - PfSPZ Vaccine

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=8; Two doses of 9.0 x 10\^5 PfSPZ Vaccine administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 3C has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 3D - Normal Saline

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=4; Two doses of normal saline administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 3C has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 1: Grp 3E - PfSPZ Vaccine

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=8; Two doses of 1.8 x 10\^6 PfSPZ Vaccine administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 3D has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 1: Grp 3E - Normal Saline

Children aged 5-12 months (inclusive) of age will be enrolled in this group.

N=4; Two doses of normal saline administered DVI, 8 weeks apart. The 1st dose will be administered 2 weeks after Grp 3D has been shown to be well-tolerated and without safety concerns. The 2nd dose will be administered 8 weeks after the 1st dose in this group does not show any safety signals.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Part 2: Group 1 - PfSPZ Vaccine

Infants aged 5-12 months (inclusive) of age at vaccination will be enrolled in Part 2.

N=104; the highest dose that is determined to be safe and well tolerated in the Part 1 trial, administered in 3 doses by DVI at 0, 8 and 16 weeks. Likely dosage will be 1.8 x 10\^6 PfSPZ per dose.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 2: Group 2 - PfSPZ Vaccine

Infants aged 5-12 months (inclusive) of age at vaccination will be enrolled in Part 2.

N=104; the second highest dose, which is half of the highest dose, administered in 3 doses by DVI at 0, 8 and 16 weeks. Likely dosage will be 9.0 x 10\^5 PfSPZ per dose.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 2: Group 3 - PfSPZ Vaccine

Infants aged 5-12 months (inclusive) of age at vaccination will be enrolled in Part 2.

N=104; a lower dose (half of the second highest dose) administered in 3 doses by DVI at 0, 8, 16 weeks. Likely dosage will be 4.5x 10\^5 PfSPZ per dose.

Group Type EXPERIMENTAL

PfSPZ Vaccine

Intervention Type BIOLOGICAL

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Part 2: Group 4 - Normal Saline

Infants aged 5-12 months (inclusive) of age at vaccination will be enrolled in Part 2.

N=104; a placebo arm, will receive normal saline by DVI, 3 times at 8 week intervals.

Group Type PLACEBO_COMPARATOR

Normal Saline

Intervention Type OTHER

0.9% Sodium chloride

Interventions

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PfSPZ Vaccine

Aseptic, purified, cryopreserved, radiation-attenuated Plasmodium falciparum sporozoites

Intervention Type BIOLOGICAL

Normal Saline

0.9% Sodium chloride

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Healthy children 5 months - 9 years inclusive (Part 1) and healthy infants 5-12 months inclusive (Part 2)
* HIV negative
* Able to participate for the duration of the study.
* Parents/guardians over the age of 18 years able and willing to provide informed consent/permission. The consent/permission will be in writing. For adult parents or guardians who are illiterate, an impartial witness can sign the consent/permission form on behalf of the parent and the parent/guardian will provide a thumb print.

Exclusion Criteria

* Positive HIV test or breastfeeding infants or children of a known HIV positive mother (per Kenyan guidelines, these HIV exposed breastfeeding children should be on cotrimoxazole)
* Refusal of HIV testing
* Elevated ALT (liver function test) ≥2x ULN ( ALT \>84 U/L)
* Abnormal hematological parameters defined as: hemoglobin \< 8 g/dl, WBC \<1500 / mm3, neutrophils \<750/ mm3, platelet count \<75.000/ mm3
* Abnormal renal function test with creatinine \>0.9 mg/dL
* Known sickle cell disease and other inherited blood cell disorders like thalassemia and G6PD deficiency
* Current use of systemic immunosuppressant pharmacotherapy
* Current significant medical condition (cardiac, hepatic, renal, or hematological) or evidence of any other serious underlying medical condition identified by medical history, physical examination, or laboratory examination
* History of a splenectomy
* History of neurologic disorder (including seizures, other than uncomplicated febrile seizures)
* Known allergy to any component of the vaccine formulation, history of anaphylactic response to mosquito-bites, or known allergy to first or second line anti-malarials used to treat malaria
* Plan to participate in another investigational vaccine/drug research during or within 1 month of this study end
* Prior participation in a malaria vaccine trial
* Participation in the PfSPZ Vaccine Trial Part 1 (for Part 2 only)
* History of any other illness or condition which, in the investigator's judgment, may substantially increase the risk associated with the subject's participation in the protocol or compromise the scientific objectives
* Child/orphan in institutional care
Minimum Eligible Age

5 Months

Maximum Eligible Age

9 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Kenya Medical Research Institute

OTHER

Sponsor Role collaborator

Centers for Disease Control and Prevention

FED

Sponsor Role collaborator

National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

University of Maryland

OTHER

Sponsor Role collaborator

Sanaria Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Martina Oneko, MD

Role: PRINCIPAL_INVESTIGATOR

Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya

Locations

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Center for Global Health Research, KEMRI

Kisian, Siaya County, Kenya

Site Status

Countries

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Kenya

References

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Oneko M, Steinhardt LC, Yego R, Wiegand RE, Swanson PA, Kc N, Akach D, Sang T, Gutman JR, Nzuu EL, Dungani A, Kim Lee Sim B, Oloo PN, Otieno K, Bii DK, Billingsley PF, James ER, Kariuki S, Samuels AM, Jongo S, Chebore W, Abdulla S, Daubenberger C, Mpina M, Styers D, Potter GE, Abarbanell G, Richie TL, Hoffman SL, Seder RA. Safety, immunogenicity and efficacy of PfSPZ Vaccine against malaria in infants in western Kenya: a double-blind, randomized, placebo-controlled phase 2 trial. Nat Med. 2021 Sep;27(9):1636-1645. doi: 10.1038/s41591-021-01470-y. Epub 2021 Sep 13.

Reference Type DERIVED
PMID: 34518679 (View on PubMed)

Oneko M, Cherop YR, Sang T, Gutman JR, Wiegand R, Nyang'au EM, Odila AD, Akach D, Hamel MJ, Samuels AM, Kariuki S, Abebe Y, Nzuu EL, Wijayalath W, James ER, Sim BKL, Billingsley PF, Richie TL, Hoffman SL, Seder RA, Steinhardt LC. Feasibility of direct venous inoculation of the radiation-attenuated Plasmodium falciparum whole sporozoite vaccine in children and infants in Siaya, western Kenya. Vaccine. 2020 Jun 15;38(29):4592-4600. doi: 10.1016/j.vaccine.2020.05.008. Epub 2020 May 19.

Reference Type DERIVED
PMID: 32444192 (View on PubMed)

Steinhardt LC, Richie TL, Yego R, Akach D, Hamel MJ, Gutman JR, Wiegand RE, Nzuu EL, Dungani A, Kc N, Murshedkar T, Church LWP, Sim BKL, Billingsley PF, James ER, Abebe Y, Kariuki S, Samuels AM, Otieno K, Sang T, Kachur SP, Styers D, Schlessman K, Abarbanell G, Hoffman SL, Seder RA, Oneko M. Safety, Tolerability, and Immunogenicity of Plasmodium falciparum Sporozoite Vaccine Administered by Direct Venous Inoculation to Infants and Young Children: Findings From an Age De-escalation, Dose-Escalation, Double-blind, Randomized Controlled Study in Western Kenya. Clin Infect Dis. 2020 Aug 14;71(4):1063-1071. doi: 10.1093/cid/ciz925.

Reference Type DERIVED
PMID: 31555824 (View on PubMed)

Other Identifiers

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CDC IRB Protocol #6787

Identifier Type: OTHER

Identifier Source: secondary_id

KEMRI/SERU/CGHR/017/3129

Identifier Type: -

Identifier Source: org_study_id

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