Bridging Trial to Evaluate the Infectivity Equivalence of Current and New Lots of Plasmodium Falciparum Strain 3D7 Within the WRAIR Controlled Human Malaria Infection (CHMI) Model



Status:Not yet recruiting
Conditions:Infectious Disease, Infectious Disease
Therapuetic Areas:Immunology / Infectious Diseases
Healthy:No
Age Range:18 - 50
Updated:3/22/2019
Start Date:March 25, 2019
End Date:June 5, 2019
Contact:Jason Heryla, MBA
Email:jason.m.heryla.ctr@mail.mil
Phone:301-619-8985

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BRIDGING TRIAL TO EVALUATE THE INFECTIVITY EQUIVALENCE OF CURRENT AND NEW LOTS OF PLASMODIUM FALCIPARUM STRAIN 3D7 WITHIN THE WRAIR CONTROLLED HUMAN MALARIA INFECTION (CHMI) MODEL

Objectives:

Primary:

• To characterize the infectivity of the new lot of Plasmodium falciparum strain 3D7 within
the standard WRAIR CHMI model as compared to the current lot (historical data)

Secondary:

- To assess safety of the new lot of P falciparum parasites

- To assess the kinetics of detecting parasitemia and parasite clearance by quantitative
polymerase chain reaction (qPCR) as compared to blood smear

- To obtain plasma samples to restore the testing control pool for malaria serology
testing and for future malaria research

This is a single center, open label CHMI study. CHMI will consist of exposure to Plasmodium
falciparum sporozoites through the bites of infected mosquitoes. After the challenge,
subjects will be evaluated daily for the development of malaria infection using a blood
smear. Unless previously diagnosed and fully treated, subjects will be required to stay in a
hotel for a maximum of 12 nights starting on or around the evening of Day 7 post challenge.

All subjects diagnosed with malaria infection based on smears will be prescribed a standard
malaria treatment regimen to begin on the day that parasitemia is detected. Subjects who do
not become parasitemic (via smear) by Day 19 will be empirically treated for malaria.

After the hotel phase, all challenged subjects will have a final scheduled follow-up visit on
Day 28 (±7 days).

Inclusion Criteria:

- To be eligible for this study, you must meet ALL of the following conditions:

- You are between the ages of 18 and 50 years old.

- You are willing and able to participate in all planned study visits for the
duration of the study.

- You are in good general health based on your medical history, physical
examination, EKG, and screening laboratories.

- You are able to understand and sign this informed consent.

- You pass the written test called the 'Assessment of Understanding' with a score
of at least 80% (8 out of 10 questions correct).

- You agree not to donate blood during the study and for 3 years after the malaria
challenge.

- You agree not to travel to place(s) where there is malaria during the time of the
study.

- If you are a female, you must agree to consistently use effective birth control
(e.g., oral or implanted contraceptives, intrauterine device (IUD), diaphragm
with spermicide, abstinence, cervical cap) during the period from the day of
screening (today) through 3 months after the malaria challenge.

- You must be willing to take anti-malarial treatment after CHMI, if indicated.

- You must agree to stay in a pre-determined hotel near the NMRC CTC during the
designated post-CHMI follow-up period from approximately 7 days after malaria
challenge until antimalarial treatment is completed, if indicated.

- If you are an active duty military or federal employee, you must have approval
from your supervisory chain to participate. The appropriate approval form will be
provided to you.

Exclusion Criteria:

- You must not have any of the following:

- Any history of malaria infection or having been given a malaria vaccine

- Any history travel to a country with falciparum malaria in the past 6 months, or
planned travel to such an area during the course of the study

- Any history of having lived in an area with falciparum malaria for more than 5
years.

- Any use of medications that prevent or treat malaria during the 1 month prior to
challenge or planned use during the study (outside of the drugs provided by the
study team).

- Any serious medical illness or condition involving the heart, liver, lungs, or
kidneys

- Any significant risk for developing heart disease in the next 5 years. The risk
for developing heart disease in the next 5 years will be determined by a
combination of the following factors: high blood pressure, smoking, weight,
family history of heart disease and the presence of diabetes

- Any medical illness or condition involving your blood or immune system (to
include sickle cell trait or thalassemia trait)

- Any abnormal (as determined by a physician) screening laboratory test results

- Any history of neurologic disease (including migraines or seizures)

- Any history of psoriasis (itchy skin rash) or porphyria (rare disturbance of
metabolism), since these conditions could get worse after treatment with
chloroquine (a medication for treating malaria).

- You have had your spleen removed

- Any past or current infection with HIV, Hepatitis C, or Hepatitis B

- Any use of investigational drugs or vaccines within 1 month before starting the
study

- Any allergy to or inability to take the anti-malaria medications used in this
study

- Any history of allergic reaction to mosquito bites that required hospitalization

- You must not be pregnant or nursing, or have any plans to become pregnant or
breastfeed during the period from now through 3 months after malaria challenge

- Any chronic use of steroids or other medications that affect the immune system in
the 6 months before malaria challenge. Inhaled and topical (used on the skin)
steroids are allowed.

- You plan to have surgery between enrollment and 3 months after malaria challenge.

- Any active alcohol or drug abuse

- You have any other physical or psychologic condition or laboratory abnormality
that the study doctor thinks may increase your risk of having side effects or
compromise the results of the study.
We found this trial at
1
site
Silver Spring, Maryland 20910
Principal Investigator: James E Moon, PhD
Phone: 301-319-9176
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mi
from
Silver Spring, MD
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