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Immunization of Human Volunteers With P. Vivax Irradiated Sporozoites (SPZ-Irrad)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01082341
Recruitment Status : Completed
First Posted : March 8, 2010
Last Update Posted : March 23, 2018
Sponsor:
Collaborators:
National Heart, Lung, and Blood Institute (NHLBI)
Asoclinic Inmunología Ltda.
Information provided by (Responsible Party):
Socrates Herrera Valencia, Malaria Vaccine and Drug Development Center

Brief Summary:
It is possible to safely protect human volunteers immunized with P. vivax irradiated sporozoites from P. vivax challenge with live sporozoites.

Condition or disease Intervention/treatment Phase
Malaria Biological: Immunization with P. vivax irradiated sporozoites Phase 1 Phase 2

Detailed Description:

Title: Phase 1 and Phase 2a Clinical Trial: Immunization of human volunteers with P. vivax irr-spz. (Short name: Irrad-SPZ) Population 27 healthy adult volunteers, males and non-pregnant females, between 18-45 years of age, who fulfill inclusion/exclusion criteria (described below) as determined by clinical history and serological tests. Approximately 20 parasitized blood-donor volunteers will be required to infected Anopheles mosquitoes which will be used to immunize volunteers with a total of 1000-1500 infected mosquitoes, during 8-10 months. Afterwards challenge to prove protection.

Number of Sites: 2 Study Duration: 2 years. Subject Duration : Step1: 1-2 hours to blood donors; Step 2 and 3: 2 years to immunized volunteers Objectives Primary

• To assess the safety and protective efficacy of P. vivax irradiated sporozoite vaccination.

Secondary

  • To determine the immune responses and duration elicited by the P. vivax challenge in human Fy(+) volunteers previously immunized with irr-spz, as compared with non-immunized human volunteers.
  • To determine the immune responses and duration elicited by irr-spz immunization scheme in human Fy(+) volunteers; comparing it with the same immunization scheme with non irr-spz in Fy(-) participants, and also with controls exposed to the same mosquito bite scheme as that of immunization but using mosquitoes without parasite infection.
  • To study new antigens potentially useful to induce pre-erythrocytic protection against P. vivax malaria infection

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 27 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Phase 1 and Phase 2a Clinical Trial:Immunization of Human Volunteers With P. Vivax Irradiated Sporozoites
Study Start Date : June 2012
Actual Primary Completion Date : May 2015
Actual Study Completion Date : September 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Malaria Vaccines

Arm Intervention/treatment
Experimental: Fy(+)
14 Fy(+) human volunteers in the experimental group will be immunized with 1,000-2,000 P. vivax irrad-spz bites
Biological: Immunization with P. vivax irradiated sporozoites

Anopheles albimanus mosquitoes will be infected by artificial membrane feeding using blood from P. vivax infected donors. Once mosquitoes are positive will be irradiated at 15000 cGy and kept in boxes until use.

14 Fy(+) human volunteers in the experimental group will be immunized with 1,000-2,000 P. vivax irrad-spz bites. Seven Fy(+) volunteers in the control group will be exposed to non-infected mosquito bites. Six Fy(-) volunteers will be exposed to infective mosquito bites. For the challenge both the immunized and control groups will be exposed to 3 ± 1 infective mosquito bites. Volunteers will be closely monitored post infection and will be treated with antimalarials.

Other Name: P. vivax irradiated sporozoites vaccine

Active Comparator: Fy(+) control
Seven Fy(+) volunteers in the control group will be exposed to non-infected mosquito bites.
Biological: Immunization with P. vivax irradiated sporozoites

Anopheles albimanus mosquitoes will be infected by artificial membrane feeding using blood from P. vivax infected donors. Once mosquitoes are positive will be irradiated at 15000 cGy and kept in boxes until use.

14 Fy(+) human volunteers in the experimental group will be immunized with 1,000-2,000 P. vivax irrad-spz bites. Seven Fy(+) volunteers in the control group will be exposed to non-infected mosquito bites. Six Fy(-) volunteers will be exposed to infective mosquito bites. For the challenge both the immunized and control groups will be exposed to 3 ± 1 infective mosquito bites. Volunteers will be closely monitored post infection and will be treated with antimalarials.

Other Name: P. vivax irradiated sporozoites vaccine

Active Comparator: Fy(-)
Six Fy(-) volunteers will be exposed to infective mosquito bites.
Biological: Immunization with P. vivax irradiated sporozoites

Anopheles albimanus mosquitoes will be infected by artificial membrane feeding using blood from P. vivax infected donors. Once mosquitoes are positive will be irradiated at 15000 cGy and kept in boxes until use.

14 Fy(+) human volunteers in the experimental group will be immunized with 1,000-2,000 P. vivax irrad-spz bites. Seven Fy(+) volunteers in the control group will be exposed to non-infected mosquito bites. Six Fy(-) volunteers will be exposed to infective mosquito bites. For the challenge both the immunized and control groups will be exposed to 3 ± 1 infective mosquito bites. Volunteers will be closely monitored post infection and will be treated with antimalarials.

Other Name: P. vivax irradiated sporozoites vaccine




Primary Outcome Measures :
  1. Three groups are considered to be intervened. Experimental, Control and Fy(-) groups. Comparison will be done between E and C groups for protective efficacy. For immune response tests E vs Fy(-),E vs Fy(-), and Fy(-) vs C, pairs will be compared. [ Time Frame: 2 years ]

Secondary Outcome Measures :
  1. The number of subjects reporting any AEs, the occurrence of specifics AEs, and discontinuation due to AEs will be tabulated. Frequency of AEs will be cross-tabulated by group for each immunization session [ Time Frame: 2 years ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • • Healthy 18 to 45 years old man or non-pregnant women.

    • To have the capacity to sign an informed consent in a free and voluntary way.
    • Have an acceptable understanding of the clinical trial through the approval of a questionnaire regarding the information given in the consent process.
    • Obligatory use of adequate contra-conceptive method from beginning of recruitment and screening time up to three months after last immunization
    • Do not have chronic or acute diseases. These conditions will be determined by clinical history, physical exam and laboratory tests.
    • To accept not traveling to malaria endemic areas during the clinical trial should
    • To have telephone at home or mobile phone that permit permanent contact for follow up
    • He (she) manifest that is willing to participated during both steps of the clinical trial.

Exclusion Criteria:

  • Volunteers with less than 18 old year or more than 45 old years.
  • Pregnant and suckling women will be excluded. Pregnancy will be determined both by interview, and by serum B-subunit chorionic gonadotrophin testing.
  • History of moderate or severe insect, or food allergies.
  • G-6PD deficiency or any Hb genetic defect (for example; sickle cell disease)
  • Previous malaria infection demonstrated by think smear, PCR or specific antimalarial antibodies.
  • If the subject has previously participated in a malarial vaccine trial.
  • Clinical record of allergies to drug or insect bites.
  • Symptoms, signs or data from laboratory test that suggests to the physician any systemic disorder like renal, hepatic, cardiovascular, pulmonary, psychiatric disorders or other illnesses that could interfere with results of clinical trial or could compromise the health of the volunteer.
  • To have antibodies against hepatitis C, VIH, or hepatitis B superficial antigen and/or hepatitis B core antibodies.
  • To have any abnormality in the parameters assessed by blood laboratory tests. Base-line values will be established before initiation of the clinical trial.
  • Presence or history of an auto-immune disease such as; Asthma, lupus, rheumatoid arthritis, Graves's disease, Hashimoto tyroiditis, and others.
  • History of surgical removal of the spleen (splenectomy).
  • Volunteer with medical treatment known to alter the immune system before 3 months to recruitment, such as; cortico-steroids, chemotherapeutic agents, fludarabine, cyclosporine, tacrolimus, mycophenolate mofetil, rapamycine, ATG, alemtuzumab.
  • Alcoholism or drug abuse that may interfere with social relationship of individual.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01082341


Locations
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Colombia
Malaria Vaccine of Develepmente Center
Cali, Valle, Colombia
Sponsors and Collaborators
Malaria Vaccine and Drug Development Center
National Heart, Lung, and Blood Institute (NHLBI)
Asoclinic Inmunología Ltda.
Investigators
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Principal Investigator: Socrates Herrera, MD Malaria Vaccine Develepment Center
Additional Information:
Publications:
Herrera, S., et al., Development of a sporozoite challenge model for Plasmodium vivax in human volunteers. . (Submitte), 2009
Herrera, S., et al., Implication of Plasmdium vivax sporozoite challenge system in vaccine development, in International Research in Infectious Diseases. 2007. p. 53.
Jordan-Villegas, A., et al., Cellular and humoral responses to Plasmodium vivax irradiated sporozoites in Aotus monkeys. (In preparation), 2007
López, J.A., et al., Immunogenicity of synthetic peptides corresponding to the nonrepeat regions of the P. falciparum circumsporozoite protein. Vaccines 96. Cold Spring Harbor Laboratory 1996: p. 255-260
Fernández, O., et al. Development of a sporozoite challenge model for Plasmodium vivax in human volunteers. in Annual meeting 54th American Society of Tropical Medicine and Hygiene. December 11-15. . 2005. Washington: Am Trop J Med. Hyg.
Manzano, M.R., et al., Standardization of Anopheles albimanus infection with Plasmodium vivax for sporozoite challenge of naive volunteers. (In preparation), 2009.
Hoffman, S.L., et al., Attacking the infected hepatocyte. In Malaria Vaccine Development: A Multi- Immune Response Approach, ed. S.L. Hoffman. 1996, Washington, DC: ASM Press. 35-75.

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Socrates Herrera Valencia, Director, Malaria Vaccine and Drug Development Center
ClinicalTrials.gov Identifier: NCT01082341    
Other Study ID Numbers: MVDC-2008-005
SPZ IRR HUMAN ( Other Identifier: MVDC )
5R01HL086488-02 ( U.S. NIH Grant/Contract )
First Posted: March 8, 2010    Key Record Dates
Last Update Posted: March 23, 2018
Last Verified: March 2018
Keywords provided by Socrates Herrera Valencia, Malaria Vaccine and Drug Development Center:
GCP Good Clinical Practice
IFAT Indirect Immunofluorescence antibody test
MFA Membrane Feeding Assay
N Number (typically refers to subjects)
RBC Red Blood Cells
SOP Standard Operating Procedure
TBS Thick blood smear
P. Vivax
irradiated sporozoite vaccination.
Additional relevant MeSH terms:
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Malaria
Protozoan Infections
Parasitic Diseases
Infections
Mosquito-Borne Diseases
Vector Borne Diseases
Vaccines
Immunologic Factors
Physiological Effects of Drugs